Rare key functional domain missense substitutions in MRE11A, RAD50, and NBNcontribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study
Breast Cancer Research volume 16, Article number: R58 (2014)
The MRE11A-RAD50-Nibrin (MRN) complex plays several critical roles related to repair of DNA double-strand breaks. Inherited mutations in the three components predispose to genetic instability disorders and the MRN genes have been implicated in breast cancer susceptibility, but the underlying data are not entirely convincing. Here, we address two related questions: (1) are some rare MRN variants intermediate-risk breast cancer susceptibility alleles, and if so (2) do the MRN genes follow a BRCA1/BRCA2 pattern wherein most susceptibility alleles are protein-truncating variants, or do they follow an ATM/CHEK2 pattern wherein half or more of the susceptibility alleles are missense substitutions?
Using high-resolution melt curve analysis followed by Sanger sequencing, we mutation screened the coding exons and proximal splice junction regions of the MRN genes in 1,313 early-onset breast cancer cases and 1,123 population controls. Rare variants in the three genes were pooled using bioinformatics methods similar to those previously applied to ATM, BRCA1, BRCA2, and CHEK2, and then assessed by logistic regression.
Re-analysis of our ATM, BRCA1, and BRCA2 mutation screening data revealed that these genes do not harbor pathogenic alleles (other than modest-risk SNPs) with minor allele frequencies >0.1% in Caucasian Americans, African Americans, or East Asians. Limiting our MRN analyses to variants with allele frequencies of <0.1% and combining protein-truncating variants, likely spliceogenic variants, and key functional domain rare missense substitutions, we found significant evidence that the MRN genes are indeed intermediate-risk breast cancer susceptibility genes (odds ratio (OR) = 2.88, P = 0.0090). Key domain missense substitutions were more frequent than the truncating variants (24 versus 12 observations) and conferred a slightly higher OR (3.07 versus 2.61) with a lower P value (0.029 versus 0.14).
These data establish that MRE11A, RAD50, and NBN are intermediate-risk breast cancer susceptibility genes. Like ATM and CHEK2, their spectrum of pathogenic variants includes a relatively high proportion of missense substitutions. However, the data neither establish whether variants in each of the three genes are best evaluated under the same analysis model nor achieve clinically actionable classification of individual variants observed in this study.
Based on risk and frequency, three classes of breast cancer susceptibility genes or loci are currently recognized: high-risk genes such as BRCA1 and BRCA2 (Mendelian Inheritance in Man numbers (MIMs) 113705 and 600185) in which protein-truncating mutations and severely dysfunctional missense substitutions confer a five- to ten-fold increased risk and for which the summed allele frequency in the general population is <1%; intermediate-risk genes such at ATM and CHEK2 (MIMs 208900 and 604373) in which protein-truncating mutations and severely dysfunctional missense substitutions confer a two- to five-fold increased risk and for which the summed allele frequency in the general population may approach 1%; and common, modest-risk single nucleotide polymorphisms (SNPs) which individually have much higher frequency but only rarely confer risk greater than 1.25-fold [1, 2]. Linkage analysis provided an effective genome-wide approach for locating high-risk susceptibility genes, and genome-wide association study provided an effective approach for finding risk-associated SNPs. While exome sequencing-based strategies may eventually provide a hypothesis-free, genome-wide approach for identification of intermediate-risk genes, much of our current knowledge base has flowed from candidate gene studies .
The MRN complex, formed from dimers of the proteins encoded by MRE11A, RAD50, and NBN (MIMs 600814, 604040, and 602667), plays key roles in DNA double-strand break (DSB) repair, meiotic recombination, cell cycle checkpoints, and maintenance of telomeres . In mice, homozygous knockouts of these genes are lethal [5–7]. Humans born with biallelic mutations in any one of the three genes share a cellular phenotype that includes sensitivity to ionizing radiation, a deficit in DNA DSB repair, and chromosomal instability (MIM 604391; MIM 251260) . Moreover, these people are at risk of severe cancer susceptibility phenotypes. For example, two brothers who were compound heterozygotes for mutations that fell in the amino region of the MRE11A protein died of pulmonary adenocarcinoma before age 20 [9, 10], which would seem very unlikely in the absence of an underlying cancer predisposition. Susceptibility to lymphoma is a prominent feature of Nijmegen breakage syndrome, which is caused by biallelic mutation of NBN. While too few human biallelic RAD50 mutation carriers have been identified to reach a conclusion about their cancer susceptibility, more than 20% of mice homozygous for a hypomorphic Rad50 allele (Rad50 p.Lys22Met) that lived past age four months died with lymphoma or leukemia .
Breast cancer risks for heterozygous carriers of MRN gene mutations were summarized briefly by Hollestelle et al. . Of the three genes, NBN has the strongest evidence in support of acting as an intermediate-risk breast cancer gene. This is largely because the truncating variant NBN c.657del5 has a high enough frequency among individuals of Slavic origin to be evaluated by case-control analysis, and meta-analysis of nine such studies revealed a combined odds ratio (OR) of 2.63 (95% confidence interval (CI) 1.76 to 3.93) for this variant . Most evidence in favor of RAD50 rested on a truncating variant RAD50 c.687delT which has been observed in Finnish cases and controls [14, 15]; while subsequent studies in the same and other populations are consistent with the hypothesis that RAD50 is an intermediate-risk breast or pancreatic cancer susceptibility gene, they have not provided significant supporting evidence [16, 17]. Evidence for MRE11A rests primarily on the observation of two mutations in the gene from a series of eight non-BRCA1/2 breast cancer families with tumors that showed loss of all three MRN proteins .
Previously, we performed case-control mutation screening studies of ATM, CHEK2, XRCC2, and RAD51 to clarify our understanding of their role in breast cancer susceptibility [19–22]. A common thread across these studies has been use of bioinformatic and statistical approaches designed to detect evidence of pathogenicity from both truncating and splice junction variants (T + SJV) and/or rare missense substitutions (rMS). Here, we apply a case-control mutation screening strategy in an ethnically diverse series of subjects to evaluate MRE11A, RAD50, and NBN. Given that the three proteins form an evolutionarily conserved complex involved in maintenance of genomic integrity, we decided to evaluate the three genes as a single large candidate intermediate-risk breast cancer susceptibility gene with a concatenated open reading frame of 2,774 amino acids - which nevertheless is not quite as large as the 3,056 amino acid open reading frame of ATM. Our analysis addresses two related questions: (1) are some rare MRN variants intermediate-risk breast cancer susceptibility alleles, and if so (2) do the MRN genes follow a BRCA1/2 pattern wherein most susceptibility alleles are protein-truncating variants, or do they follow an ATM/CHEK2 pattern wherein half or more of the susceptibility alleles are missense substitutions?
The design for this study has been described in detail previously [19, 20, 22]. Briefly, eligible participants included women ascertained by population-based sampling by the Australian, Northern California, and Ontario sites of the Breast Cancer Family Registry (BCFR) . Subjects were recruited between 1995 and 2005. Selection criteria for cases (N = 1,313) were diagnosis of breast cancer at or before age 45 years and self-reported race/ethnicity plus grandparents’ country of origin information consistent with Caucasian, East Asian, Hispanic/Latino, or African American racial/ethnic heritage. The controls (N = 1,123) were frequency matched to the cases within each center on racial/ethnic group, with age at selection not more than ± 10 years from the age range at diagnosis of the cases gathered from the same center. Because of the shortage of available controls in some racial/ethnic and age groups, the frequency matching was not one-to-one in all subgroups.
Recruitment and genetic studies were approved by the Ethics Committee of the International Agency for Research on Cancer (IARC), the University of Utah Institutional Review Board (IRB), and the local IRBs of the BCFR centers from which we received samples. These local IRBs were the Health Sciences Human Research Ethics Subcommittee of the University of Melbourne, Australia; the Institutional Review Board of the Cancer Prevention Institute of California; and the Research Ethics Boards of Mount Sinai Hospital and the University Health Network, Ontario, Canada. Written informed consent was obtained from each participant.
For mutation screening of the coding exons and proximal splice junction regions of MRE11A (NM_005591.3), RAD50 (NM_005732.3) and NBN (NM_002485.4), we used 30 ng of whole-genome amplified (WGA) DNA obtained by mixing 15 ng of amplified DNA from each of two independent WGA reactions. The laboratory process was as described in detail for our recent studies of ATM, CHEK2, XRCC2, and RAD51[19–22]. Our semi-automated approach, handled by a Laboratory Information Management System (LIMS) [24, 25], relies on mutation scanning by high-resolution melt curve (HRM) analysis followed by direct Sanger sequencing of the individual samples for which an aberrant melting curve profile is indicative of the presence of a sequence variant. In a previous work, we showed that the HRM technique showed high sensitivity and specificity (1.0, and 0.8, respectively, for amplicons of <400 bp) for mutation screening by comparing the results with those obtained with Sanger sequencing .
For MRN amplicons harboring a SNP(s) with frequency ≥1% in either dbSNP or initial amplicon testing, we applied a simultaneous mutation scanning and genotyping approach using HRM analysis to improve the sensitivity and the efficiency of the mutation screening, as described previously [24, 25].
All exonic sequence variants, plus intronic sequence variants that fell within 20 bp of a splice acceptor or eight bp of a splice donor, and were either unreported or had an allele frequency of <1% in the large scale reference groups ‘Caucasian Americans’, ‘African Americans’ and ‘East Asians’ based on exome variant server (EVS) and 1,000 genomes project (1000G) data [27, 28], were confirmed either by independent re-amplification and sequencing from each of the two independent WGA reaction products and concordant variant calls, or, for five variants, by re-amplification and sequencing from genomic DNA.
All samples that failed either at the primary PCR, secondary PCR, or sequencing reaction stage were re-amplified from WGA DNAs or genomic DNAs. Samples that still did not provide satisfactory mutation screening results for at least 80% of the concatenated MRN coding sequence were excluded from further analysis. Primer and probe sequences are available from the authors upon request.
Alignments and scoring of missense substitutions
We used M-Coffee , which is part of the Tree-based consistency objective function for alignment evaluation (T-Coffee) software suite of alignment tools  to prepare a protein multiple sequence alignment for each of the three MRN proteins (MRE11A, RAD50 and NBN) in order to predict the effect of missense substitutions on the proteins and on the activity of the MRN complex. Each alignment consisted of sequences from 16 species: Homo sapiens, Macaca mulatta, Callithrix jacchus, Mus musculus, either Sus scrofa or Bos Taurus, Loxodonta africana, Dasypus novemcinctus, Monodelphis domestica, Ornithorhynchus anatinus, Gallus gallus, Anolis carolinensis, either Xenopus tropicalis or Xenopus laevis, Latimeria chalumnae, either Fugu rubripes or Danio rerio, Branchiostoma lanceolatum, and Strongylocentrotus purpuratus. The alignments were characterized using the Protpars routine of Phylogeny Inference Package version 3.2 software (PHYLIP)  to make a maximum parsimony estimate of the number of substitutions that occurred along each clade of the underlying phylogeny. The sequence alignment, or updated versions thereof, is available at the Align Grantham variation Grantham deviation (Align-GVGD) website . Missense substitutions observed during our mutation screening of the three MRN genes were scored using the Align-GVGD and Sorting Intolerant from Tolerant (SIFT) software programs with our curated alignments, and with polymorphism phenotyper (PolyPhen-2.1) software using its precompiled alignments [33–35]. In brief, Align-GVGD grades missense substitutions against a protein multiple sequence alignment based on a combination of Grantham Variation (GV), which measures the amount of physicochemical variation at a particular position in the alignment, and Grantham Deviation (GD), which measures the physicochemical difference between the missense residue and the range of variation observed at its position in the protein. The classifier provides seven ordered grades (C65, C55, C45, C35, C25, C15 and C0) ranging from the most likely deleterious to least likely deleterious . SIFT is a sequence homology-based tool that predicts variants in the query sequence as ‘tolerated’ or ‘deleterious’ using normalized probabilities calculated from the input multiple sequence alignment . Variants at a position with normalized probabilities less than 0.05 are predicted deleterious and predicted neutral with a probability greater than or equal to 0.05. PolyPhen-2 predicts variants as ‘benign’, ‘possibly damaging’, or ‘probably damaging’ based on eight sequence-based and three structure-based predictive features . The alignment pipeline used in PolyPhen-2 selects homologous sequences using a clustering algorithm and then constructs and refines the alignment yielding an alignment containing both orthologs and paralogs that may or may not be full length, which yields a wider breadth of sequences but decreased depth compared with the curated alignments used with Align-GVGD and SIFT .
In silicoprediction on splicing
Sequence variants falling in the first three bp or last three bp of an exon, plus intronic variants detected in the vicinity of the splice junction sequences, with allele frequencies <1%, were scored for their potential impact on splicing using MaxEntScan (MES), which computes the maximum entropy score of a given sequence using splice site models trained on human data . In work to be published elsewhere, we calibrated MES by calculating the average and standard deviation of MES scores for the wild-type splice junctions in BRCA1, BRCA2, and ATM, allowing us to convert raw MES scores into z-scores. Based on BRCA1 and BRCA2 mutation screening data used previously to calibrate Align-GVGD [33, 38], we found that rare variants that fall within the acceptor or donor region and reduce the MES score for the splice signal in which they fall show an approximately 95% probability to damage splice junction function when they result in a calibrated MES score of z < −2, or approximately 40% probability when they result in a calibrated MES score of −2 < z ≤ −1 ; Vallee et al., manuscript in preparation. Thus these MES-based rules were used to identify rare sequence variants that are likely to alter MRN gene mRNA splicing.
Analysis of rare variant threshold frequency from ATM, BRCA1, BRCA2, and CHEK2data
For ATM, we examined the relationship between sequence variant frequency and breast cancer risk as follows. Frequencies for all of the variants included in our 2009 ATM case-control mutation screening meta-analysis  were extracted from the EVS (for Caucasian American and African American frequencies) or UK National Genetics Reference Laboratory Manchester (NGRL Manchester) summary of 1000G data (for East Asian allele frequencies) . T + SJV (as defined in ) plus missense substitutions and in-frame indels falling from position 1960 through the end of the protein were then grouped into the following allele frequency bins: 1% to 0.32%, 0.32% to 0.10%, 0.10% to 0.032%, <0.032%. ORs for each bin were then estimated by logistic regression, adjusting for study, ethnicity and mutation-screening method employed, using Stata version 11 software (StataCorp, College Station, TX, USA).
CHEK2 sequence variants included in our 2011 CHEK2 case-control mutation screening study  were evaluated in the same way except that (a) position in the protein was not considered, and (b) logistic regressions were adjusted for study center and race/ethnicity.
For BRCA1 and BRCA2, we examined the relationship between frequency and risk as follows. First we defined ‘pseudo-cases’ and ‘pseudo-controls’ from the tested population at Myriad Genetics in the data set we used to evaluate more than 1,000 BRCA1/2 sequence variants in 2007 . The data set included results from approximately 68,000 full-sequence tests. Pseudo-cases for BRCA1 were defined to be all tested individuals who were affected with breast cancer and were not found to carry a pathogenic variant in either BRCA1 or BRCA2; pseudo-controls were taken to be affected individuals who were found to carry pathogenic mutations in BRCA2 (thus explaining their personal and family history of cancer). A similar approach was taken for BRCA2 variants, with carriers of BRCA1 pathogenic variants serving as pseudo-controls. For each gene, variants were categorized into frequency bins as described above. Logistic regression was then used to estimate ORs for each frequency bin. Note that, because carriage of clearly pathogenic variants was used to differentiate between pseudo-cases and pseudo-controls, the BRCA1 and BRCA2 ORs were estimated from the distributions of unclassified variants.
Statistical analyses of MRN case-control mutation screening data
To assess the relationship between MRN variants and breast cancer risk, analyses were performed using the chi-square test and multivariable unconditional logistic regression using Stata version 11 software (StataCorp). Differences in the case-control ratio between racial/ethnic groups and study center were accounted for by including categorical variables for each racial/ethnic group and each study center. Adjustment for racial/ethnic group should also capture confounding of genetic and social factors with interaction terms, allowing that this confounding effect may be different for the broadly labeled racial/ethnic groups in different centers. P values reported from analyses of the MRN case-control data are from the likelihood ratio test, adjusted for racial/ethnic group and study center, unless otherwise noted.
Number of subjects included in the analysis
Of the 2,436 BCFR participants, three (one case from the Canadian BCFR and two controls from the Australian BCFR) were excluded because their PCR failure rate for MRN mutation-screening amplicons was greater than 20%. The distributions of the remaining 1,312 cases and 1,121 controls by age, race or ethnicity, and study center are detailed in Table 1.
Relationship between frequency and odds ratio for homologous recombination repair pathway breast cancer susceptibility genes
In our case-control mutation screening studies of ATM, CHEK2, RAD51, and XRCC2, we excluded from statistical analysis sequence variants with allele frequencies above an arbitrarily selected frequency of 0.5%. With the availability of 1000G and EVS mutation screening data, it is now possible to use external data to bin rare sequence variants into allele frequency categories and then, using independent observational data, estimate odds ratio as a function of frequency. Results of such an analysis of sequence variants from confirmed breast cancer susceptibility genes, for example, ATM, BRCA1, BRCA2, and CHEK2 are summarized in Table 2 and provide the basis for an empirically determined allele frequency threshold.
In the 0.32% to 0.10% allele frequency bin, there was significant evidence of pathogenic variants in CHEK2; indeed, the known pathogenic CHEK2 variants c.1100delC (Chr22:29091856delG) and p.Ile157Thr (rs17879961) both have allele frequencies between 0.32% and 0.10% in the EVS ‘Caucasian American’ sample. But there was no evidence for pathogenic variants in the other three genes in this allele frequency range.
In the 0.10 to 0.032% bin, BRCA2 had an OR of 1.60 (P = 0.078). Although just shy of significant, an elevated BRCA2 OR in this EVS frequency bin is supported by the presence of known pathogenic BRCA2 variants with multiple reports in the Breast Information Core (BIC) database such as c.2806_2809delAAAC (rs80359351) and c.3847_3848delGT (rs80359405) . While the OR for ATM in this frequency bin was very near 1.0, our data set did contain one known pathogenic in-frame deletion in the gene, p.RIS2547_2549del (c.7638_7646del9), which was observed in a control.
Below an allele frequency of 0.032%, all four genes had significant evidence of pathogenic variants. We note that, in genotype-phenotype terms, the MRN genes more closely resemble BRCA1, BRCA2, and ATM than CHEK2 in that inheritance of biallelic mutations in the MRN genes is either embryonic lethal or causes a developmental phenotype that severely reduces reproductive fitness; we know of no such evidence for biallelic CHEK2 mutation carriers [42–44]. Therefore, noting that there was no evidence for pathogenic variants in ATM, BRCA1, or BRCA2 with allele frequencies >0.1% in continental level populations, we set our threshold for evaluating rare MRN variants at an allele frequency ≤0.1% in Caucasian Americans, African Americans, and East Asians, based on EVS data for the former two groups and 1000G data, as summarized by the NGRL Manchester, for East Asian allele frequencies .
Analyses of rare silent substitutions and rare, analytically innocuous splice junction variants
Full open reading frame mutation screening of the MRN genes revealed 20 rare silent substitutions and 21 splice junction variants that look innocuous by the MaxEntScan based sequence analysis criteria described in the Methods (Table S1 in Additional file 1). Accounting for subjects who carried two rare variants, 10 cases and 10 controls carried a rare silent substitution and no other potentially more severe rare variant, resulting in an OR of 0.95 (P = 0.91). Similarly, 14 cases and 13 controls carried an innocuous rare splice junction variant and no other potentially more severe rare variant, resulting in an OR of 0.62 (P = 0.25) (Table 3).
Analysis of protein-truncating variants
Full open reading frame mutation screening of the MRN genes revealed three nonsense substitutions, five frameshift variants, one severely damaging splice donor variant, one severely damaging splice acceptor variant, and two moderately damaging splice donor variants (Table 4 and Table S1 in Additional file 1). Of these 12 variants, only one, RAD50 c.2938del5, was carried by more than one subject (two controls). In addition, one of these 12 variants, RAD50 c.3852del4, falls in a final coding exon where it would not trigger nonsense-mediated decay. Analytically, we considered this as being analogous to an in-frame deletion and included the variant in our analyses of rMS and in-frame deletions rather than our analysis of T + SJV. With nine T + SJV observations in cases against three in controls, the OR for T + SJV was 2.61, P = 0.14 (Table 5).
Analyses of rare missense substitutions and in-frame indels
We observed 58 distinct rMS, one in-frame deletion, and one final exon frameshift (RAD50 c.3852del4) that we treated as an in-frame deletion (Table S1 in Additional file 1). Taking into account that two subjects (one case and one control) carried two rMS, these added up to 48 cases and 38 controls that carried one or more rMS or in-frame indel. The OR for this class of variants was 0.96 (P = 0.85) (Table 3).
In our analyses of BRCA1 and BRCA2, we found that evidence for pathogenic, non-spliceogenic, missense substitutions in those genes was limited to substitutions that fall in the protein’s key functional domains and have severity scores of greater than C0 when evaluated by Align-GVGD [33, 38]; that observation is also supported by an extensive functional assay analysis of BRCA1 missense substitutions . In our case-control mutation screening analysis of ATM, we also found that evidence for rMS that predispose to breast cancer was limited to rMS with Align-GVGD severity scores of greater than C0 that fall in the key functional domains of the protein that are central to its enzymatic activity . Accordingly, we carried out an analysis of MRN gene rMS limited to these key functional domains, largely as described in a recent review of MRN protein structure and function  with the exception that we excluded from the analysis variants falling in the second DNA binding domain of MRE11A because this domain is required for DSB formation during meiosis but not for repair of DSBs .
Limited to the key functional domains as annotated on Figure 1 (which is derived from Williams et al. ), and excluding the second DNA binding domain of MRE11A, we observed 23 rMS and one final exon truncating variant that we evaluate as an in-frame deletion (RAD50 c.3852del4). These variants were carried by 24 cases and five controls, resulting in an OR of 3.17 (P = 0.012) (Table 5 and Table S1 in Additional file 1).
To refine analyses of the key domain rMS, we prepared and hand-curated protein multiple sequence alignments of the MRN proteins. Each alignment contains 16 sequences from MRN orthologs and, from the perspective of the position of Homo sapiens in the vertebrate phylogeny, each samples the same key nodes of mammalian and vertebrate evolution. The concatenated alignment slightly exceeds an average of 3.0 substitutions per position, reaching our criterion of sufficient sequence diversity for evaluating missense substitutions . Using these alignments, the key domain rMS were scored with Align-GVGD and SIFT; PolyPhen-2 scores for these variants were also extracted from PolyPhen’s pre-computed exome-wide data set [32, 64, 65]. The key domain final exon truncating variant RAD50 c.3852del4 was assigned Align-GVGD, SIFT, and PolyPhen-2 scores corresponding to the most severe missense substitution created by the frameshifted coding; these were C65, 0.00, and 0.996, respectively (Align-GVGD and PolyPhen-2 scales have the opposite polarity of the SIFT scale; all three of these scores are indicative of an extremely damaging variant). Accordingly, for all further analyses described here, RAD50 c.3852del4 is included in the most severe grade of key domain rMS unless otherwise noted.
A conservative view of protein multiple sequence alignment-based evaluation of human missense substitutions is that each missense substitution that falls within or very close to the range of variation observed at its position in an appropriately informative alignment should be neutral or nearly so. With Align-GVGD, this would correspond to missense substitutions that score C0. Using the complete alignments of the MRN proteins, 11 of the key domain rMS scored C0; these were carried by 11 cases and just one control, potentially indicative of overly stringent alignment depth. Reducing the stringency of the Align-GVGD scoring by restricting the alignments to the mammals-only subset (comprising sequences from nine species), four of the key domain rMS scored C0, and these were carried by four cases and one control. Excluding these four substitutions as likely innocuous, the 20 remaining key domain rMS were carried by 20 cases and four controls (Table 5 and Table S1 in Additional file 1). The OR for the non-C0 key domain rMS and in-frame deletions was 3.07 (P = 0.029).
Exploiting the intrinsic ordering of the seven Align-GVGD grades from C0 to C65, we performed a logistic regression test for log-linear OR trends across noncarriers and carriers of the seven grades of rMS. In this test, the C0 substitutions are again considered very likely neutral and assigned a severity grade of 0, which was the same as the grade assigned to noncarriers. The more severe grades were assigned sequentially higher severities, with C65 substitutions assigned a severity grade of 6 (Tables 4 and 6). The test yielded a lognormal OR increase of 0.21/grade (P = 0.077), which corresponds to a modeled OR of 3.60 at grade 6 (Table 6).
Truncating variants and rare missense substitutions assessed in a single model
Using a simple binary classification to combine T + SJV plus key functional domain rMS of grade > C0 into a single model, we observed 29 carriers among the cases against seven among the controls. This binary classification resulted in an OR of 2.88, P = 0.0090 (Table 5).
To add the T + SJV into the regression test for OR trend across the graded rMS, we assigned protein-truncating variants a severity grade equal to that of the highest grade rMS included in that regression, in this case 6.0. Potentially damaging splice junction variants were assigned this severity grade x their probability to damage a splice junction, that is, severely damaging splice junction variants were assigned a severity grade of 0.95 × 6 = 5.7, and moderately damaging splice junction variants a severity grade of 0.40 × 6 = 2.4. This test yielded a lognormal OR increase of 0.18/grade (P = 0.033), which corresponds to a modeled OR of 2.89 at the most severe grade (Table 6).
In addition to the lognormal OR coefficient and modeled OR at the most severe sequence variant grade, Table 6 also reports the OR point estimate at the most severe sequence variant grade. One unusual result was that, for the analysis or rMS, the logistic regression adjustment for race/ethnicity and study center decreased the modeled OR for key domain C65 rMS by 42% and decreased the OR point estimated for this class of rMS by 58% compared to the crude result. These ORs also decreased in the combined test of rMS plus T + SJV, but not as dramatically.
Looking at the underlying data, 11 of the 12 observations of key domain C65 rMS - including both controls that carried such a variant - were carried by either an East Asian or a Latina. Because the case:control ratio in these groups was 3:1 (Table 1), the adjustment for race/ethnicity applies a relatively high weight to the genotypes of the East Asian and Latina controls, explaining the marked decrease in the OR point estimates upon adjustment. As clustering of C65 rMS in the East Asian and Latina subjects was an unexpected heterogeneity in our data set, we checked for heterogeneity across racial/ethnic groups by class of likely pathogenic sequence variant (Table 7). While there was no evidence for heterogeneity in the distributions of T + SJV or rMS in general, subset analysis found racial/ethnic heterogeneity across the key domain rMS (P = 0.003) and sub-subset analysis found that this heterogeneity was localized exclusively to the key domain C65 variants (P = 0.96 for rMS of grade C0 to C55, but P <1x10−5 for C65 rMS). To examine the impact of racial/ethnic heterogeneity in the distribution of key domain C65 rMS on the evidence in favor of the MRN genes as intermediate-risk breast cancer susceptibility genes, we assessed the key domain C65 missense substitutions alone and re-ran the binary analysis of T + SJV and key domain rMS with the C65 variants excluded (Table 8). The crude OR for key domain C65 missense substitutions alone was 4.3, but dropped to 1.78 upon adjustment for race/ethnicity and study center. Nonetheless, excluding these C65 rMS from the binary analysis of T + SJV and key domain rMS resulted in an OR of 3.39 (Table 5), and the P value (P = 0.010) was virtually identical to that observed when the C65 rMS were included (P = 0.0090). Similarly, setting aside the issue of racial/ethnic heterogeneity by limiting the binary analysis of T + SJVs and key domain rMS to Caucasians of European ancestry resulted in an OR of 4.08 (P = 0.0068) (Table 8). Finally, exclusion of the key domain C65 rMS from the graded test of rMS and T + SJV resulted in a lognormal OR increase of 0.33/grade (P = 0.021) and virtually no change in the OR coefficient upon adjustment (Table 6). Thus the racial/ethnic heterogeneity in the distribution of these rMS does not impinge on the overall result of this study. Of note, among the key domain C65 rMS, the RAD50 zinc hook domain missense substitution p.Arg725Trp was observed in three Latina cases; the EVS reports that the variant was observed in 1 of 2,200 African Americans and the variant was not present in 1000G data.
In the present work, we evaluated the contribution of rare variants in the genes MRE11A, RAD50, and NBN to breast cancer risk. As the proteins encoded by these genes form an evolutionarily conserved complex that could be functionally impaired by a dysfunctional variant in any one of the genes, we evaluated them as if they constitute a single candidate susceptibility gene. Combining T + SJV, and key functional domain rMS, we found that this set of rare MRN genes variants contributes to breast cancer susceptibility (OR = 2.88, P = 0.0090). A post hoc test for heterogeneity did not reveal evidence for between-gene differences in the case-control distributions of likely pathogenic variants: Fisher’s exact test P values of between-gene heterogeneity for T + SJV, key domain rMS and the combination of the two classes of rare variants were 0.43, 1.00, and 0.53, respectively (Table 7). Similarly, looking at the genes individually, neither truncating variants, nor key domain missense substitutions, nor a combination of the two reached statistical significance from single gene data (Table 9). Thus evidence from this study in favor of the MRN genes as intermediate-risk breast cancer susceptibility genes emerges from the ensemble analysis of the three genes.
Although MRN gene T + SJV were not by themselves a significant breast cancer risk factor, we note that our OR point estimate of 2.61 is both very close to the meta-analysis point estimate of 2.63 that Zhang et al. obtained for NBN c.657del5 , and close to the point estimate of 2.32 that we obtained in our meta-analysis of ATM T + SJV . Thus, while we cannot exclude that our nonsignificant finding is actually indicative of little or no risk of breast cancer conferred by MRN gene protein-truncating variants, our data are more strongly in accord with the hypothesis that they confer an intermediate risk of magnitude similar to the risk conferred by truncating variants in ATM.
Overall, there was no association between rMS and risk of breast cancer. Nevertheless, tightening the focus to key functional domain rMS resulted in a significant association with an OR of approximately 3.0. In this sense, the MRN genes behave as the homologous recombination repair genes BRCA1, BRCA2, and ATM - genes in which rare missense substitutions that are pathogenic because of missense dysfunction per se are largely confined to key functional domains.
Combining MRN T + SJV and key functional domain rMS, we observed an OR of 2.88 with a P value of 0.0090. That P value meets the threshold of P <0.01 that Hollestelle et al. suggested for establishing intermediate-risk susceptibility genes that were already strong candidates based on their biochemical function . Thus with a mutation screening and data analysis approach that considered MRE11A, RAD50, and Nibrin as a unique functional entity and focused the analysis of rMS to those that fall in the key functional domains of the MRN complex, we overcame the limitation of previous suggestive studies that were based on a small number of founder mutations [13, 15, 18], and confirmed the hypothesis that MRE11A, RAD50, and NBN are intermediate-risk susceptibility genes in a general sense. Moreover, because we did not observe any of the four sequence variants most responsible for the MRN genes’ candidate gene status (MRE11A p.Arg202Gly, MRE11A p.Arg633Stop, RAD50 c.687delT, and NBN c.657del5) [13, 14, 18], this confirmation is independent of the hypothesis-generating data.
Five of the sequence variants observed in the MRN case-control mutation screening bear further discussion.
NBN p.Arg215Trp was of interest because association studies have found evidence that it confers modest risk of several cancers (for review, see ), and there is biochemical evidence, albeit somewhat conflicting, of altered function of this nibrin allele [67, 68]. We observed six cases and six controls with the p.Arg215Trp missense substitution, resulting in an OR of 0.96 (95% CI 0.30 to 3.06, P = 0.95). While these confidence intervals are too wide to exclude the possibility that NBN p.Arg215Trp is actually a modest-risk variant, we also point out that position Arg215 is quite variable in our protein multiple sequence alignment and that, according to EVS data, the variant has a frequency of 0.37% in Caucasian Americans - well above the frequency threshold we found for severely dysfunctional variants in homologous recombination repair genes in which biallelic mutations cause embryonic lethality or severe childhood disease.
Second, we observed one carrier, a Caucasian control ascertained at the age of 55, of the MRE11A in-frame deletion c.2109del9. The variant falls in the last exon of the gene, near the carboxy terminus of the second DNA binding domain (which is also the carboxy terminus of the protein). Because this domain is required for double-strand break formation during meiosis but not for repair of double-strand breaks , the domain was not included in the list of ‘key functional domains’ and the indel was not included in statistical analyses of key functional domain variants.
Third, we observed one carrier, an East Asian case diagnosed at the age of 35, of MRE11A p.Thr481Ile. This residue is a threonine in all but one species in our alignment, but is a methionine in the cephalochordate, Branchiostoma lanceolatum. The substitution falls within the protein’s RAD50 interaction domain. While very few of the rare variants that we observed have been reported in human ataxia-telangiectasia-like disease or Nijmegen breakage syndrome patients, another substitution at this residue, p.Thr481Lys, was observed in an Italian ataxia-telangiectasia-like disease sib-pair .
Fourth, we observed one carrier, an East Asian control ascertained at age 50, of the RAD50 frameshift c.3852del4. Because the frameshift falls in the last exon of the gene where it would not be expected to cause nonsense-mediated decay of the mRNA, we evaluated it as an in-frame deletion rather than as a frameshift. As such, it scrambles well-conserved sequence near the carboxy terminus of the protein’s carboxy-end ATPase domain and final MRE11A binding domain including positions such as Arg1288 and Lys1291 that are invariant in our protein multiple sequence alignment. The sequence scrambling creates nonconservative substitutions at invariant key functional domain positions, resulting in the highest possible sequence variant severity score.
Fifth, we observed one carrier, also an East Asian control ascertained at age 50, of the NBN missense substitution p.Ile35Thr. This position falls in the protein’s functionally important forkhead-associated (FHA) domain and is either isoleucine or leucine in all of the species included in our NBN protein multiple sequence alignment.
The last three variants described above illustrate two of the analytic problems encountered in this study. All three were evaluated as key domain C65 rMS and all three were observed in East Asian subjects. Combined with eight additional observations of key domain C65 rMS in either East Asian or Latina subjects against just one in a Caucasian of European ancestry, there was an unexpected excess of these variants in the non-Caucasian subjects mutation screened in this study. Second, the two variants observed in the controls affected positions with little or no cross-species physicochemical variability; consequently, they would be graded as severe C65 variants with either a mammals-only protein multiple sequence alignment or with our complete alignment through the deuterostomate Strongylocentrotus purpuratus. In contrast, the MRE11A rMS that described from a breast cancer case (p.Thr481Ile), as well as the rMS observed at the same position in a pair of ataxia-telangiectasia-like disease cases (p.Thr481Lys), score as severe C65 substitutions when evaluated with the mammals-only alignment but as likely innocuous C0 substitutions when evaluated with the evolutionarily deep alignment. Since the observation of a nonconservative rMS at MRE11A position Thr481 in a pair of ataxia-telangiectasia-like disease cases increases the odds that substitutions at this position are in fact pathogenic, it appears that using the evolutionarily deeper alignments is, for the MRN genes, counterproductive. On the other hand, the empirically determined allele frequency thresholds derived by combining older ATM, BRCA1, BRCA2, and CHEK2 case-control mutation screening data with EVS and 1000G data - found to be 0.1% for the three genes (ATM, BRCA1, and BRCA2) where inheritance of biallelic mutations is either embryonic lethal or causes a developmental phenotype that severely reduces reproductive fitness, and 0.32% for CHEK2 - provides a new tool to help with evaluation of the many rare variants observed in a case-control mutation screening study of candidate cancer susceptibility genes.
For BRCA1 and BRCA2, it is well established that a strong majority of pathogenic variants are, ultimately, protein-truncating variants. In contrast, case-control mutation screening of CHEK2 revealed an approximately equal contribution from T + SJVs and rMSs to the fraction of breast cancer attributable to rare variants in that gene, and a case-control mutation screening meta-analysis of ATM revealed that rMS in that gene may actually be responsible for a larger fraction of the breast cancer attributable to rare variants than are the T + SJVs [19, 20]. In the mutation screening data reported here, rare key functional domain missense substitutions in the MRN genes were more frequent (24 vs. 12 observations) than truncating variants and conferred a slightly higher OR (3.07 vs. 2.61) with a lower P value (0.029 vs. 0.14). These data are more congruent with the ATM/CHEK2 pattern than the BRCA1/2 pattern. Since there is not yet any efficient approach to clinically actionable classification of missense substitutions in these genes, these data point toward a clinical problem. When the MRN genes are mutation screened as part of a clinical panel-based cancer susceptibility gene sequencing test, a large fraction, if not the majority, of the genetic risk attributable to them will reside in rare missense substitutions that will initially be reported to clinical geneticists as unclassified variants.
The analytic strategy of treating the three genes as a single concatenated gene had one notable drawback: we are not able to ask whether variants in each of the three genes are best evaluated under the same analysis model. Thus an enormous amount of work, likely involving larger scale mutation screening efforts to gain more analytic precision, tests of segregation to examine penetrance and tumor spectrum, and perhaps development of functional assays to aid evaluation of rare missense substitutions, remains to be performed on with MRE11A, RAD50, and NBN.
Results reported here establish that MRE11A, RAD50, and NBN are intermediate-risk breast cancer susceptibility genes and help to justify their inclusion on panel-based cancer susceptibility gene tests. Protein-truncating variants and rare missense substitutions falling in the key functional domains of these proteins appear to confer two- to three-fold increased risk of breast cancer. Like ATM and CHEK2, the spectrum of pathogenic variants in the MRN genes includes a relatively high proportion of missense substitutions. However, the data neither establish whether variants in each of the three genes are best evaluated under the same analysis model nor achieve clinically actionable classification of individual variants observed in this study. Given the relatively low frequency of likely pathogenic variants in the MRN genes, development of clinically applicable rare missense substitution classification models for these genes will require data from very large observational studies supplemented, in all likelihood, by carefully calibrated functional assays.
1000 genomes project
Align Grantham variation Grantham deviation
ataxia telangiectasia mutated
Breast Cancer Family Registry
Breast Cancer Information Core
Breast Cancer 1 gene
BRCA1 and/or BRCA2
Breast Cancer 2 gene
checkpoint kinase 2
Canadian Institutes for Health Research
exome variant server
high-resolution melting curve analysis
International Agency for Research on Cancer
Institutional Review Board
Mendelian Inheritance in Man
- MRE11A :
meiotic recombination 11
- MRN complex:
- NBN :
United States National Cancer Institute
- NGRL Manchester:
UK National Reference Laboratory Manchester
United States National Institutes of Health
polymerase chain reaction
Phylogeny Inference Package
rare missense substitution
Sorting Intolerant from Tolerant
- T- or M-Coffee:
Tree-based consistency objective function for alignment evaluation
- T + SJV:
truncating and splice junction variants
- WGA DNA:
whole-genome amplified deoxyribonucleic acid
X-ray cross complemention group 2.
Genetic susceptibility. World Cancer Report 2008. Edited by: Boyle P, Levin B. 2008, Lyon: IARC Press, 183-184.
Michailidou K, Hall P, Gonzalez-Neira A, Ghoussaini M, Dennis J, Milne RL, Schmidt MK, Chang-Claude J, Bojesen SE, Bolla MK, Wang Q, Dicks E, Lee A, Turnbull C, Rahman N, Fletcher O, Peto J, Gibson L, Dos Santos Silva I, Nevanlinna H, Muranen TA, Aittomaki K, Blomqvist C, Czene K, Irwanto A, Liu J, Waisfisz Q, Meijers-Heijboer H, Adank M, van der Luijt RB, et al: Large-scale genotyping identifies 41 new loci associated with breast cancer risk. Nat Genet. 2013, 45: 353-361. 361e1-2
Hollestelle A, Wasielewski M, Martens JW, Schutte M: Discovering moderate-risk breast cancer susceptibility genes. Curr Opin Genet Dev. 2010, 20: 268-276.
Williams GJ, Lees-Miller SP, Tainer JA: Mre11-Rad50-Nbs1 conformations and the control of sensing, signaling, and effector responses at DNA double-strand breaks. DNA Repair (Amst). 2010, 9: 1299-1306.
Xiao Y, Weaver DT: Conditional gene targeted deletion by Cre recombinase demonstrates the requirement for the double-strand break repair Mre11 protein in murine embryonic stem cells. Nucleic Acids Res. 1997, 25: 2985-2991.
Luo G, Yao MS, Bender CF, Mills M, Bladl AR, Bradley A, Petrini JH: Disruption of mRad50 causes embryonic stem cell lethality, abnormal embryonic development, and sensitivity to ionizing radiation. Proc Natl Acad Sci U S A. 1999, 96: 7376-7381.
Zhu J, Petersen S, Tessarollo L, Nussenzweig A: Targeted disruption of the Nijmegen breakage syndrome gene NBS1 leads to early embryonic lethality in mice. Curr Biol. 2001, 11: 105-109.
Waltes R, Kalb R, Gatei M, Kijas AW, Stumm M, Sobeck A, Wieland B, Varon R, Lerenthal Y, Lavin MF, Schindler D, Dork T: Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder. Am J Hum Genet. 2009, 84: 605-616.
Uchisaka N, Takahashi N, Sato M, Kikuchi A, Mochizuki S, Imai K, Nonoyama S, Ohara O, Watanabe F, Mizutani S, Hanada R, Morio T: Two brothers with ataxia-telangiectasia-like disorder with lung adenocarcinoma. J Pediatr. 2009, 155: 435-438.
Regal JA, Festerling TA, Buis JM, Ferguson DO: Disease-associated MRE11 mutants impact ATM/ATR DNA damage signaling by distinct mechanisms. Hum Mol Genet. 2013, 22: 5146-5159.
van der Burgt I, Chrzanowska KH, Smeets D, Weemaes C: Nijmegen breakage syndrome. J Med Genet. 1996, 33: 153-156.
Bender CF, Sikes ML, Sullivan R, Huye LE, Le Beau MM, Roth DB, Mirzoeva OK, Oltz EM, Petrini JH: Cancer predisposition and hematopoietic failure in Rad50(S/S) mice. Genes Dev. 2002, 16: 2237-2251.
Zhang ZH, Yang LS, Huang F, Hao JH, Su PY, Sun YH: Current evidence on the relationship between two polymorphisms in the NBS1 gene and breast cancer risk: a meta-analysis. Asian Pac J Cancer Prev. 2012, 13: 5375-5379.
Heikkinen K, Karppinen SM, Soini Y, Makinen M, Winqvist R: Mutation screening of Mre11 complex genes: indication of RAD50 involvement in breast and ovarian cancer susceptibility. J Med Genet. 2003, 40: e131-
Heikkinen K, Rapakko K, Karppinen SM, Erkko H, Knuutila S, Lundan T, Mannermaa A, Borresen-Dale AL, Borg A, Barkardottir RB, Petrini J, Winqvist R: RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability. Carcinogenesis. 2006, 27: 1593-1599.
Tommiska J, Seal S, Renwick A, Barfoot R, Baskcomb L, Jayatilake H, Bartkova J, Tallila J, Kaare M, Tamminen A, Heikkila P, Evans DG, Eccles D, Aittomaki K, Blomqvist C, Bartek J, Stratton MR, Nevanlinna H, Rahman N: Evaluation of RAD50 in familial breast cancer predisposition. Int J Cancer. 2006, 118: 2911-2916.
Wang X, Szabo C, Qian C, Amadio PG, Thibodeau SN, Cerhan JR, Petersen GM, Liu W, Couch FJ: Mutational analysis of thirty-two double-strand DNA break repair genes in breast and pancreatic cancers. Cancer Res. 2008, 68: 971-975.
Bartkova J, Tommiska J, Oplustilova L, Aaltonen K, Tamminen A, Heikkinen T, Mistrik M, Aittomaki K, Blomqvist C, Heikkila P, Lukas J, Nevanlinna H, Bartek J: Aberrations of the MRE11-RAD50-NBS1 DNA damage sensor complex in human breast cancer: MRE11 as a candidate familial cancer-predisposing gene. Mol Oncol. 2008, 2: 296-316.
Tavtigian SV, Oefner PJ, Babikyan D, Hartmann A, Healey S, Le Calvez-Kelm F, Lesueur F, Byrnes GB, Chuang SC, Forey N, Feuchtinger C, Gioia L, Hall J, Hashibe M, Herte B, McKay-Chopin S, Thomas A, Vallee MP, Voegele C, Webb PM, Whiteman DC, Sangrajrang S, Hopper JL, Southey MC, Andrulis IL, John EM, Chenevix-Trench G: Rare, evolutionarily unlikely missense substitutions in ATM confer increased risk of breast cancer. Am J Hum Genet. 2009, 85: 427-446.
Le Calvez-Kelm F, Lesueur F, Damiola F, Vallee M, Voegele C, Babikyan D, Durand G, Forey N, McKay-Chopin S, Robinot N, Nguyen-Dumont T, Thomas A, Byrnes GB, Hopper JL, Southey MC, Andrulis IL, John EM, Tavtigian SV: Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study. Breast Cancer Res. 2011, 13: R6-
Park DJ, Lesueur F, Nguyen-Dumont T, Pertesi M, Odefrey F, Hammet F, Neuhausen SL, John EM, Andrulis IL, Terry MB, Daly M, Buys S, Le Calvez-Kelm F, Lonie A, Pope BJ, Tsimiklis H, Voegele C, Hilbers FM, Hoogerbrugge N, Barroso A, Osorio A, Giles GG, Devilee P, Benitez J, Hopper JL, Tavtigian SV, Goldgar DE, Southey MC: Rare mutations in XRCC2 increase the risk of breast cancer. Am J Hum Genet. 2012, 90: 734-739.
Le Calvez-Kelm F, Oliver J, Damiola F, Forey N, Robinot N, Durand G, Voegele C, Vallee MP, Byrnes G, Registry BC, Hopper JL, Southey MC, Andrulis IL, John EM, Tavtigian SV, Lesueur F: RAD51 and breast cancer susceptibility: no evidence for rare variant association in the Breast Cancer Family Registry Study. PLoS One. 2012, 7: e52374-
John EM, Hopper JL, Beck JC, Knight JA, Neuhausen SL, Senie RT, Ziogas A, Andrulis IL, Anton-Culver H, Boyd N, Buys SS, Daly MB, O’Malley FP, Santella RM, Southey MC, Venne VL, Venter DJ, West DW, Whittemore AS, Seminara D: The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer. Breast Cancer Res. 2004, 6: R375-R389.
Voegele C, Tavtigian SV, de Silva D, Cuber S, Thomas A, Le Calvez-Kelm F: A Laboratory Information Management System (LIMS) for a high throughput genetic platform aimed at candidate gene mutation screening. Bioinformatics. 2007, 23: 2504-2506.
Nguyen-Dumont T, Calvez-Kelm FL, Forey N, McKay-Chopin S, Garritano S, Gioia-Patricola L, De Silva D, Weigel R, Sangrajrang S, Lesueur F, Tavtigian SV: Description and validation of high-throughput simultaneous genotyping and mutation scanning by high-resolution melting curve analysis. Hum Mutat. 2009, 30: 884-890.
Garritano S, Gemignani F, Voegele C, Nguyen-Dumont T, Le Calvez-Kelm F, De Silva D, Lesueur F, Landi S, Tavtigian SV: Determining the effectiveness of High Resolution Melting analysis for SNP genotyping and mutation scanning at the TP53 locus. BMC Genet. 2009, 10: 5-
The exome variant server. [http://evs.gs.washington.edu/EVS/]
1000 Genomes. [http://browser.1000genomes.org/index.html]
Wallace IM, O’Sullivan O, Higgins DG, Notredame C: M-Coffee: combining multiple sequence alignment methods with T-Coffee. Nucleic Acids Res. 2006, 34: 1692-1699.
Felsenstein J: PHYLIP - Phylogeny Inference Package (version 3.2). Cladistics. 1989, 5: 164-166.
Align GVGD. [http://agvgd.iarc.fr]
Tavtigian SV, Byrnes GB, Goldgar DE, Thomas A: Classification of rare missense substitutions, using risk surfaces, with genetic- and molecular-epidemiology applications. Hum Mutat. 2008, 29: 1342-1354.
Kumar P, Henikoff S, Ng PC: Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm. Nat Protoc. 2009, 4: 1073-1081.
Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, Bork P, Kondrashov AS, Sunyaev SR: A method and server for predicting damaging missense mutations. Nat Methods. 2010, 7: 248-249.
Tavtigian SV, Greenblatt MS, Lesueur F, Byrnes GB: In silico analysis of missense substitutions using sequence-alignment based methods. Hum Mutat. 2008, 29: 1327-1336.
Yeo G, Burge CB: Maximum entropy modeling of short sequence motifs with applications to RNA splicing signals. J Comput Biol. 2004, 11: 377-394.
Easton DF, Deffenbaugh AM, Pruss D, Frye C, Wenstrup RJ, Allen-Brady K, Tavtigian SV, Monteiro AN, Iversen ES, Couch FJ, Goldgar DE: A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes. Am J Hum Genet. 2007, 81: 873-883.
Vallee MP, Francy TC, Judkins MK, Babikyan D, Lesueur F, Gammon A, Goldgar DE, Couch FJ, Tavtigian SV: Classification of missense substitutions in the BRCA genes: a database dedicated to Ex-UVs. Hum Mutat. 2012, 33: 22-28.
NGRL 1000 Genomes Variant Access. [https://secure.ngrl.org.uk/1kg_querytool/]
Breast cancer information core. [http://research.nhgri.nih.gov/projects/bic/index.shtml]
van Puijenbroek M, van Asperen CJ, van Mil A, Devilee P, van Wezel T, Morreau H: Homozygosity for a CHEK2*1100delC mutation identified in familial colorectal cancer does not lead to a severe clinical phenotype. J Pathol. 2005, 206: 198-204.
Adank MA, Jonker MA, Kluijt I, van Mil SE, Oldenburg RA, Mooi WJ, Hogervorst FB, van den Ouweland AM, Gille JJ, Schmidt MK, van der Vaart AW, Meijers-Heijboer H, Waisfisz Q: CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women. J Med Genet. 2011, 48: 860-863.
Huijts PE, Hollestelle A, Balliu B, Houwing-Duistermaat JJ, Meijers CM, Blom JC, Ozturk B, Krol-Warmerdam EM, Wijnen J, Berns EM, Martens JW, Seynaeve C, Kiemeney LA, van der Heijden HF, Tollenaar RA, Devilee P, van Asperen CJ: CHEK2*1100delC homozygosity in the Netherlands-prevalence and risk of breast and lung cancer. Eur J Hum Genet. 2013, 22: 46-51.
Bouwman P, van der Gulden H, van der Heijden I, Drost R, Klijn CN, Prasetyanti P, Pieterse M, Wientjens E, Seibler J, Hogervorst FB, Jonkers J: A high-throughput functional complementation assay for classification of BRCA1 missense variants. Cancer Discov. 2013, 3: 1142-1155.
Usui T, Ohta T, Oshiumi H, Tomizawa J, Ogawa H, Ogawa T: Complex formation and functional versatility of Mre11 of budding yeast in recombination. Cell. 1998, 95: 705-716.
InterPro protein sequence analysis and classification. [http://www.ebi.ac.uk/interpro/]
NCBI conserved domains database. [http://www.ncbi.nlm.nih.gov/Structure/cdd/cdd.shtml]
Marchler-Bauer A, Lu S, Anderson JB, Chitsaz F, Derbyshire MK, DeWeese-Scott C, Fong JH, Geer LY, Geer RC, Gonzales NR, Gwadz M, Hurwitz DI, Jackson JD, Ke Z, Lanczycki CJ, Lu F, Marchler GH, Mullokandov M, Omelchenko MV, Robertson CL, Song JS, Thanki N, Yamashita RA, Zhang D, Zhang N, Zheng C, Bryant SH: CDD: a Conserved Domain Database for the functional annotation of proteins. Nucleic Acids Res. 2011, 39: D225-D229.
Schiller CB, Lammens K, Guerini I, Coordes B, Feldmann H, Schlauderer F, Mockel C, Schele A, Strasser K, Jackson SP, Hopfner KP: Structure of Mre11-Nbs1 complex yields insights into ataxia-telangiectasia-like disease mutations and DNA damage signaling. Nat Struct Mol Biol. 2012, 19: 693-700.
Hopfner KP, Karcher A, Craig L, Woo TT, Carney JP, Tainer JA: Structural biochemistry and interaction architecture of the DNA double-strand break repair Mre11 nuclease and Rad50-ATPase. Cell. 2001, 105: 473-485.
Williams RS, Moncalian G, Williams JS, Yamada Y, Limbo O, Shin DS, Groocock LM, Cahill D, Hitomi C, Guenther G, Moiani D, Carney JP, Russell P, Tainer JA: Mre11 dimers coordinate DNA end bridging and nuclease processing in double-strand-break repair. Cell. 2008, 135: 97-109.
Lammens K, Bemeleit DJ, Mockel C, Clausing E, Schele A, Hartung S, Schiller CB, Lucas M, Angermuller C, Soding J, Strasser K, Hopfner KP: The Mre11:Rad50 structure shows an ATP-dependent molecular clamp in DNA double-strand break repair. Cell. 2011, 145: 54-66.
Williams GJ, Williams RS, Williams JS, Moncalian G, Arvai AS, Limbo O, Guenther G, SilDas S, Hammel M, Russell P, Tainer JA: ABC ATPase signature helices in Rad50 link nucleotide state to Mre11 interface for DNA repair. Nat Struct Mol Biol. 2011, 18: 423-431.
Lim HS, Kim JS, Park YB, Gwon GH, Cho Y: Crystal structure of the Mre11-Rad50-ATPgammaS complex: understanding the interplay between Mre11 and Rad50. Genes Dev. 2011, 25: 1091-1104.
Dery U, Coulombe Y, Rodrigue A, Stasiak A, Richard S, Masson JY: A glycine-arginine domain in control of the human MRE11 DNA repair protein. Mol Cell Biol. 2008, 28: 3058-3069.
Boisvert FM, Dery U, Masson JY, Richard S: Arginine methylation of MRE11 by PRMT1 is required for DNA damage checkpoint control. Genes Dev. 2005, 19: 671-676.
Hopfner KP, Karcher A, Shin DS, Craig L, Arthur LM, Carney JP, Tainer JA: Structural biology of Rad50 ATPase: ATP-driven conformational control in DNA double-strand break repair and the ABC-ATPase superfamily. Cell. 2000, 101: 789-800.
Williams RS, Dodson GE, Limbo O, Yamada Y, Williams JS, Guenther G, Classen S, Glover JN, Iwasaki H, Russell P, Tainer JA: Nbs1 flexibly tethers Ctp1 and Mre11-Rad50 to coordinate DNA double-strand break processing and repair. Cell. 2009, 139: 87-99.
Lloyd J, Chapman JR, Clapperton JA, Haire LF, Hartsuiker E, Li J, Carr AM, Jackson SP, Smerdon SJ: A supramodular FHA/BRCT-repeat architecture mediates Nbs1 adaptor function in response to DNA damage. Cell. 2009, 139: 100-111.
Falck J, Coates J, Jackson SP: Conserved modes of recruitment of ATM, ATR and DNA-PKcs to sites of DNA damage. Nature. 2005, 434: 605-611.
You Z, Chahwan C, Bailis J, Hunter T, Russell P: ATM activation and its recruitment to damaged DNA require binding to the C terminus of Nbs1. Mol Cell Biol. 2005, 25: 5363-5379.
di Masi A, Antoccia A: NBS1 heterozygosity and cancer risk. Curr Genomics. 2008, 9: 275-281.
di Masi A, Viganotti M, Polticelli F, Ascenzi P, Tanzarella C, Antoccia A: The R215W mutation in NBS1 impairs gamma-H2AX binding and affects DNA repair: molecular bases for the severe phenotype of 657del5/R215W Nijmegen breakage syndrome patients. Biochem Biophys Res Commun. 2008, 369: 835-840.
Dzikiewicz-Krawczyk A, Mosor M, Januszkiewicz D, Nowak J: Impact of heterozygous c.657–661del, p.I171V and p.R215W mutations in NBN on nibrin functions. Mutagenesis. 2012, 27: 337-343.
Delia D, Piane M, Buscemi G, Savio C, Palmeri S, Lulli P, Carlessi L, Fontanella E, Chessa L: MRE11 mutations and impaired ATM-dependent responses in an Italian family with ataxia-telangiectasia-like disorder. Hum Mol Genet. 2004, 13: 2155-2163.
We wish to thank all participants in the BCFR for their contribution to the study. We also appreciate the support of J. McKay and the Genetic Cancer Susceptibility group at IARC.
This work was supported by the United States National Institutes of Health (NIH) National Cancer Institute (NCI) grant R01 CA121245, by the Canadian Institutes of Health Research (CIHR) for the CIHR Team in Familial Risks of Breast Cancer program, by the Government of Canada through Genome Canada and the Canadian Institutes of Health Research, and the Ministère de l’enseignement supérieur, de la recherche, de la science, et de la technologie du Québec through Génome Québec. The BCFR was supported by grant UM1 CA164920 from the NCI. The work also benefited from the Huntsman Cancer Institute’s Bioinformatics Shared Resource, which is supported by NCI grant P30 CA042014. The content of this manuscript does not necessarily reflect the views or policies of the NCI or any of the collaborating centers in the BCFR, nor does mention of trade names, commercial products, or organizations imply endorsement by the U.S. Government or the BCFR.
The authors declare that they have no competing interests.
FD led the mutation screening of RAD50, contributed to data analysis, and helped to draft the manuscript. MP led the mutation screening of NBN, contributed to data analysis, and helped to draft the manuscript. JO led the mutation screening of MRE11A, contributed to data analysis, and helped to draft the manuscript. FLCK contributed to study design, led the laboratory team, and helped to draft the manuscript. CV was responsible for data management throughput for the project, helped to refine the laboratory platform, and helped to draft the manuscript. ELY built and curated the MRN protein multiple sequence alignments, helped with scoring missense substitutions, and helped to draft the manuscript. NR contributed to the mutation screening and data analysis, helped to refine the laboratory platform, and helped to draft the manuscript. NF contributed to the mutation screening and data analysis, helped to refine the laboratory platform, and helped to draft the manuscript. GD contributed to the mutation screening and data analysis, helped to refine the laboratory platform, and helped to draft the manuscript. MPV built the algorithm for evaluating splice junction variants and helped to draft the manuscript. KT contributed to evaluation of splice junction variants and helped to draft the manuscript. TCR adapted the splice junction analysis algorithm to run on sequence variants written in genome coordinates and helped to draft the manuscript. GJW defined the coordinates of the MRN protein key functional domains and helped to draft the manuscript. JLH was the lead investigator for subjects gathered through the Australian site of the BCFR and helped to draft the manuscript. MCS contributed to study design, contributed to the management of samples obtained through the Australian site of the BCFR, and helped to draft the manuscript. ILA was the lead investigator for subjects gathered through the Ontario site of the BCFR and helped to draft the manuscript. EMJ was the lead investigator for subjects gathered through the Northern California site of the BCFR and helped to draft the manuscript. DEG contributed to study design, contributed to the analysis of rare variants in BRCA1 and BRCA2, gave advice on analysis of the MRN data, and helped to draft the manuscript. FL contributed to study design and data analysis, and helped to draft the manuscript. SVT was responsible for overall study design, contributed to data analysis, and helped to draft the manuscript. All authors read and approved the final manuscript.
Francesca Damiola, Maroulio Pertesi, Javier Oliver contributed equally to this work.
Electronic supplementary material
Additional file 1: Table S1: This spreadsheet contains anonymized coded observational data sufficient to perform most of the analyses of the MRN case-control mutation screening data described in this manuscript. (XLSX 402 KB)
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Damiola, F., Pertesi, M., Oliver, J. et al. Rare key functional domain missense substitutions in MRE11A, RAD50, and NBNcontribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study. Breast Cancer Res 16, R58 (2014). https://doi.org/10.1186/bcr3669