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Diagnostic mRNA splicing assay for variants in BRCA1 and BRCA2 identified two novel pathogenic splicing aberrations
Hereditary Cancer in Clinical Practicevolume 17, Article number: 14 (2019)
Pathogenic variants in BRCA1 and BRCA2 cause hereditary breast and ovarian cancer. Screening of these genes has become easily accessible in diagnostic laboratories. Sequencing and copy number analyses are used to detect pathogenic variants, but also lead to identification of variants of unknown clinical significance (VUS). If the effect of a VUS can be clarified, it has direct consequence for the clinical management of the patient and family members. A splicing assay is one of several tools that might help in the classification of VUS. We therefore established mRNA analyses for BRCA1 and BRCA2 in the diagnostic laboratory in 2015. We hereby report the results of mRNA analysis variants in BRCA1 and BRCA2 after three years.
Variants predicted to alter splicing and variants within the canonical splice sites were selected for splicing analyses. Splicing assays were performed by reverse transcription-PCR of patient RNA. A biallalic expression analysis was carried out whenever possible.
Twenty-five variants in BRCA1 and BRCA2 were analyzed by splicing assays; nine showed altered transcripts and 16 showed normal splicing patterns. The two novel pathogenic variants in BRCA1 c.4484 + 3 A > C and c.5407–10G > A were characterized.
We conclude that mRNA analyses are useful in characterization of variants that may affect splicing. The results can guide classification of variants from unknown clinical significance to pathogenic or benign in a diagnostic laboratory, and thus be of direct clinical importance.
Pathogenic variants in BRCA1 and BRCA2 cause hereditary breast and ovarian cancer. Since the discovery of the genes more than 20 years ago [1,2,3], clinical testing has gradually become more available and comprehensive. As the methods have developed, resulting in cheaper and faster analyses, more patients are given the opportunity to have a genetic test and the tests have expanded from a few founder mutations to full gene testing of BRCA1 and BRCA2, and more recently additional genes.
Full sequencing and copy number analyses of BRCA1 and BRCA2 have the obvious advantage of finding more disease causing variants compared to a limited analysis. A disadvantage is the identification of variants of unknown clinical significance (VUS), and variant interpretation has become a major challenge.
It is of great importance to investigate, if possible, if a variant is pathogenic or not, as it may affect the clinical management of the patient and relatives, including disease screening, prevention and treatment. Multifactorial models have been developed to help classify variants. The international consortium ENIGMA (Evidence-Based Network for the Interpretation of Germline Mutant Alleles) was initiated in 2009 . A main goal was to assess the association of genetic variants with cancer predisposition through collaboration between researchers and clinicians, collecting and combining information on genetic variants in the breast cancer genes. The multifactorial method integrates data from several different independent sources such as family history, cosegregation with disease in families, and co-occurrence of a variant in trans with a pathogenic mutation. This is a favourable approach when there is enough available information on a specific variant. However, many variants are rare, and gathering enough information to reach a conclusion regarding pathogenicity in a multifactorial analysis is not always possible. Suitable functional analyses may therefore be of great value.
For exonic variants there are several ways in which a variant can alter the protein or its function, including missense, nonsense and frameshift. In addition to this, any variant, both exonic and intronic, can potentially affect splicing . There are still limitations in knowledge and tools to identify all variants that alter splicing. However, we do have bioinformatic tools to predict splicing effects of variants in or near the consensus splice site with reasonable sensitivity and specificity . These bioinformatic prediction tools are useful to select variants for functional splicing analysis, which can then confirm or disprove the predicted effect.
A variant within a consensus splice site will usually be reported as a variant of unknown significance unless additional information is available, even if there is no prediction of altered splicing. In this setting, a splicing assay can be valuable in reclassification from a VUS to a benign variant. Variants within the canonical splice site will usually be classified as likely pathogenic unless other information is available. Most canonical splice site variants are pathogenic, but there are known exceptions. Some variants within the canonical splice sites lead to naturally occurring in-frame isoforms that may rescue gene functionality. For BRCA1 and BRCA2 such variants are listed in the ENIGMA BRCA1/2 Gene Variant Classification Criteria (Table 6 in version 2.5.12017). So even in the case of a canonical splice site variant, a functional study to confirm -or possibly disprove- the effect on splicing is of great value.
Our laboratory established a diagnostic mRNA splicing assay for BRCA1 and BRCA2 in 2015, based on the recommendations published by ENIGMA . Variants predicted to lead to loss of a splice site, introduction of a new splice site, or activation of a cryptic splice site and variants within the consensus splice site were selected for mRNA splicing analysis. Here we report the results after three years of diagnostic functional splicing analysis for BRCA1 and BRCA2.
Selection criteria for RNA analysis
Variants were selected for RNA analysis based on the results of sequencing of BRCA1 and BRCA2 in patients undergoing diagnostic or predictive genetic testing for hereditary breast and ovarian cancer. Variants within a consensus splice site were selected for RNA analysis, regardless of splicing prediction as recommended by ENIGMA . A consensus splice site was defined as the last three nucleotides of the exon and the first six of the intron (donor splice site) and last twenty nucleotides of an intron and the two first of the next exon (acceptor splice site) .
Identified variants that were predicted to disrupt or create a splice site were also included regardless of their localization within or outside splice sites. The Alamut software was used for splicing predictions. The four tools SpliceSiteFinder-like, MaxEntScan, NNSPLICE and GeneSplicer, were used, on the basis of a resource analysis by National Genetics Reference Laboratory in Manchester “Splice Site Tools, A Comparative Analysis Report by Hellen B (http://www.ngrl.org.uk/Manchester/)”. We considered a reduction in the splice site score by 10–20% by at least three of the tools as significant. The score of the normal splice site was taken into account. The prediction of a new splice site was considered significant if at least three of the tools recognized the putative new splice site. Again, the score, and the distance to the normal splice site was considered. When in doubt, we had a liberal approach in choosing variants for RNA analysis. We also included some variants where the literature showed divergent or inconclusive results, even though the variant did not meet our criteria for splicing assay.
As we were establishing a new method in our laboratory, we decided to include variants that had been analyzed by splicing assays by others for the purpose of validation.
The DNA and mRNA variant numbering is based on the cDNA sequence for BRCA1 (GeneBank: NM_007294.3) and BRCA2 (GeneBank: NM_000059.3). The BRCA1 and BRCA2 nomenclature follows the recommendations from the Human Genome Variation Society (HGVS), where A in the translation initiation codon ATG is base c.1 (http://varnomen.hgvs.org/). Exons are numbered systematically (1…n) in BRCA1 and BRCA2, which may differ from previous publications where exon numbering of BRCA1 is based on historical numbering of exons (1,2,3,5…n).
Blood samples, RNA extraction and reverse transcriptase PCR
Blood from patients undergoing genetic testing at Oslo University Hospital, and control blood samples from voluntary blood bank donors, was drawn and stored in PAXgene Blood RNA tubes according to manufacturer’s recommendations. RNA was extracted using the PAXgene Blood RNA kit (both from Preanalytix, Qiagen, Hombreachtikon, Switzerland), according to the recommended protocols (PreAnalytiX) including DNAse treatment. cDNA was generated using the SuperScript Vilo cDNA Synthesis Kit (Invitrogen, Carlsbad, California, USA), using 150 ng input RNA.
Transcript analysis was carried out by recommendations given by ENIGMA . PCR for fragment analysis was performed using AmpliTaq Gold 360 DNA Polymerase (Applied Biosystems, Foster City, California, USA). Reverse primers were tagged with FAM at the 5′ end for detection by Capillary electrophoresis (CE). The PCR fragments were separated by CE on ABI 3730xl DNA analyzer and using GeneScan™ 1200 LIZ® dye Size Standard (both from Applied Biosystems). CE analysis was performed with GeneMarker software (SoftGenetics, Pennsylvania, USA).
All patient samples were amplified in duplicates. Two to three controls from individuals not carrying the variant were always amplified in parallel with patient samples. In order to avoid allele drop out due to failure of primers to anneal, all patients were checked for single nucleotide polymorphisms (SNPs) in the primer annealing sequence. Sequencing was carried out on ABI 3730xl DNA analyzer (Applied Biosystems) using BigDye Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems).
For variants with that affected splicing, we assessed if the variant induced partial or complete splicing aberration, as recommended by ENIGMA . This was achieved by specifically amplifying the wild-type transcript including a heterozygous exonic variant, whenever this was possible. In addition, if possible, a region including a heterozygous exonic variant was amplified in order to determine expression of both alleles in samples with no effect on splicing.
Based on the results of the analyses, each variant was given a splice class as defined by Houdayer et al. ; Class 3S: Severe impact on splicing/the mutant allele does not produce the wild type transcript, complete effect, 2S: impact on alternative splicing/leaky splice site mutation, partial effect, and Class 1S: no effect on splicing with identification of the two alleles using informative SNPs.
Out of the 25 variants analyzed in the splicing assay, nine showed altered splicing (Table 1). All nine of the aberrant transcripts had altered reading frames, eventually leading to premature stop codons. Five of these had been assessed in different functional splicing assays before, and our results were consistent with those of other studies. Four of the variants have not been characterized by functional studies before, as far as we know. Two of these showed complete pathogenic splicing aberrations. Unfortunately, for the other two novel variants we were not able to assess whether the altered splicing was partial or complete. Sixteen variants had normal splicing pattern (Table 2). We were able to demonstrate biallelic expression for 12 of these sixteen variants.
Variants with altered transcripts
Two novel pathogen splicing variants in BRCA1 were identified; c.4484 + 3 A > C and c.5407–10G > A. The variant BRCA1 c.4484 + 3A > C led to complete skipping of exon 14, which results in a disruption of the open reading frame (Fig. 1). The variant BRCA1 c.5407–10G > A showed retention of 8 bases of intron 22 i the mutant transcript (Fig. 2). There was no normal transcript produced from the variant alleles.
Two additional novel variants leading to abnormal splicing were identified, BRCA1 c.5332 + 4A > G and BRCA2 c.8754 + 5G > C, unfortunately we were not able to show if the aberration was complete or partial in these cases and could thus not draw any conclusion about pathogenicity. BRCA1 c.5332 + 4A > G led to skipping of exon 20, which disrupts the open reading frame. BRCA2 c.8754 + 5G > C led to retention of 46 bases of the 5′-end of intron 21 in the mutant transcript.
Five of the variants with altered splicing had been published before. The detected transcripts and references to the literature are listed in Table 1. Four were pathogenic due to complete aberrations of the reading frame; BRCA1 c.4484G > A led to skipping of exon 13. BRCA1 c.4675G > A led to a complete loss of the last 11bases of exon 14. BRCA2 c.631 + 4A > G led to complete skipping of exon 7. BRCA2 c.8331 + 2 T > C led to a complete skipping of exon 18, whereas BRCA2 c.7992 T > A led to a partial skipping of exon 18, which is a naturally occurring minor alternative transcript. BRCA2 c.7992 T > A increased the amount of this alternative transcript.
Variants with normal transcripts
Sixteen variants showed normal splicing (Table 2). Twelve of them were demonstrated to have normal transcripts produced by both alleles. Of these, seven were intronic variants and one was a synonymous exonic variant. These eight variants could be classified as benign on the basis of the splicing results. Four of these variants; BRCA1 c.594-20A > G, c.4676-8C > G and c.4987-4 T > G and BRCA2 c.7436-4A > G had not been analyzed by a splicing assay before as far as we know.
We report the results of a splicing assay for a number of variants, some with aberrations and some with normal results. In both cases, the results are of significant clinical utility.
All the detected abnormal transcripts resulted in premature stop codons. Transcripts containing premature termination codons are degraded by nonsense-mediated mRNA decay (NMD), unless they are localized less than 50 nucleotides upstream of the position of the terminal intron [10, 11]. We concluded that the variants that gave rise to only transcripts with premature stop codons are pathogenic as they are all appear in parts of the gene where we expect them to be degraded by NMD.
We characterized two novel pathogenic splicing variants, BRCA1 c.5407–10G > A and c.4484 + 3A > C. BRCA1 c.5407–10G > A had been reported as VUS in the ClinVar database (a database on the relationships between human variations and phenotypes) and listed once in the genome Aggregation Database (gnomAD) (> 246,000 alleles). BRCA1 c.4484 + 3A > C had not been reported before to our knowledge, neither in publications nor in databases. We classified these two variants as pathogenic as both led to complete splicing aberrations which altered the reading frame leading to premature stop codon; BRCA1 c.5407–10G > A through retention of eight intronic bases, and BRCA1 c.4484 + 3A > C thorough skipping of exon 13 (the same transcript as for BRCA1 c.4484G > A). In these two cases the mRNA results directly affected the clinical management of the patient. In addition, their relatives were given the opportunity to undergo predictive genetics testing, giving carriers the possibility to opt for disease screening and/or prevention.
For the other two novel variants with abnormal splicing, we were unfortunately not able to draw any conclusions about pathogenicity. BRCA1 c.5332 + 4A > G had been reported in ClinVar, three times as a variant of unknown significance and one registration as likely pathogen by CIMBA, but without provided evidence for the conclusion. BRCA1 c.5332 + 4A > G was listed four times in gnomAD (> 246,000 alleles). BRCA2 c.8754 + 5G > C led to retention of 46 bases of the 5′-end of intron 21 in the mutant transcript. This variant has not been reported before to our knowledge, neither in publications, nor in databases, but the same transcript has previously been found for another pathogenic variant in the close vicinity, namely BRCA2 c.8754 + 3 .
Five of the variants with aberrant splicing had been published before. The methods used for splicing assay were slightly different, but we detected the same transcripts and came to the same conclusions regarding pathogenicity for these variants. The two known pathogenic BRCA1 variants, c.4484G > A and c.4675G > A, had both been published with functional studies in patient RNA in 2012 [6, 13]. They have since been reported by different laboratories in ClinVar and in different populations. BRCA1 c.4484G > A leading to skipping of exon 13 (previously known as exon 14) has been reported in patients in France , Australia  and Brasil . BRCA1 c.4675G > A leading to loss of the last 11bases of exon 14 (previously known as exon 15) has been reported in patients in Germany  and Lithuania . The variant BRCA2 c.631 + 4A > G was found in a Danish breast and ovarian cancer family and analyzed with a combination of minigene and RT-PCR with the conclusion of a disease causing mutation . The variant BRCA2 c.8331 + 2 T > C has been reported several times in ClinVar and is assumed to be pathogenic because of the localization in the canonical donor splice site. However, it was only in 2017, that the result of a functional assay was published, a mingene assay that demonstrated 87% exon 18 skipping . We confirmed a complete pathogenic exon 18 skipping in a patient sample.
BRCA2 c.7992 T > A led to a partial skipping of exon 18, which is a naturally occurring minor alternative transcript . BRCA2 c.7992 T>A increased the amount of the alternative transcript lacking exon 18. This variant remains a variant of unknown significance, consistent with the conclusion drawn by Fraile-Bethencourt et al. . They quantified the ratio between the transcripts produced by this variant in a minigene assay and found 69% of the normal transcript and 31% of the transcript lacking exon 18.
Sixteen variants showed normal splicing. Twelve of them were demonstrated to have normal transcripts produced by both alleles. Of these, seven were intronic variants and one was a synonymous exonic variant. We classified these eight variants as benign based on the results of the splicing assay. To our knowledge, we are the first to report the results of a splicing assay for four of these, including BRCA1 c.594-20A > G, c.4676-8C > G and c.4987-4 T > G and BRCA2 c.7436-4A > G. These variants are rare (reported in gnomAD once, eighteen, two and four times, respectively).
Four of the variants with normal splicing pattern were exonic variants leading to amino acid substitutions, which have to be assessed separately regarding a potential effect on protein function, but we can at least rule out major splicing aberrations. Three of these exonic variants (BRCA1 c.441G > C p.(Leu147Phe) and BRCA2 c.7006C > T p.(Arg2336Cys) and c.9257G > C p.(Gly3086Ala)) had not been analyzed in a splicing assay before, as far as we know.
Three BRCA1 variants c.81-13C > G, c.81-14C > G and c.4676-8C > G were predicted to attenuate the acceptor splice site. For two of these, c.81-13C > G and c.4676-8C > G, we and others, demonstrated normal splicing. For BRCA1 c.81-14C > G, we detected only normal transcripts, but were unfortunately not able to demonstrate biallelic expression and could therefore not draw a firm conclusion. BRCA1 c.81–13 lies in the polypyrimidine tract. Even though the substitution of a C with a G interferes with the polypyrimidine stretch, there are still 16 pyrimidines in a row, so we assume that the substitution does not affect the qualities of the tract. The same argument would apply for BRCA1 c.81-14C > G. For the variant BRCA1 c.4676-8C > G, the pyrimidne tract is shorter, but closer to the intron-exon boundery, which could be an explenation for preserved normal splicing .
The fact that several of the variants, both the pathogenic and the normal ones, are very rare, illustrate the need for functional studies for variant classification in these cases.
When it comes to selecting variants for splicing assays, ideally one should analyze all variants, as any variant could potentially affect splicing . There is no efficient way to do this yet. Sensitivity of splicing prediction tools is highest in the vicinity of consensus splice sites, whereas predictions of variant effect on splicing enhancers, silencers and branchpoint have poor specificity . Bioinformatic predictions must be confirmed by functional mRNA analysis.
Overall, there was a good concordance between splicing predictions and results of mRNA analyses. All variants that altered transcription were predicted to do so. However, in line with others, we demonstrated that even if the bioinformatic tools are successful in predicting reduction in a splice site, they may not be able to discriminate between activation of a new site versus exon skipping . For the variants that maintained a normal splicing pattern, a few were predicted to alter splicing. These were located in the polypyrimidine tract. It is known that the polypyrimidine tract is quite variable from gene to gene and intron to intron. The function of the polypyrimidine tract is dependent in a number of factors, including total length of the tract, number of consecutive pyrimidines, distance to the intron-exon boundary, distance to the branch point and strength of the branch point [21, 22]. It seems that the variation in all these factors might make it difficult to predict whether a single change in the polypyrimidine tract results in altered splicing or not, by the bioinformatic tools, giving us another example of the benefit of splicing assays.
Minigene assays are valuable in assessing splicing effects of a variant, especially if there is no available patient mRNA [19, 23]. An advantage with this method is the investigation of the expression of one allele at a time. However, as the transcription takes place in a different environment than a human cell, and discrepancies in results from minigenes and patient samples have been reported, confirmation in patient RNA is recommended if possible. We confirmed the result of minigene reported by others in patient RNA for a couple of the variants. A disadvantage with the patient RNA method is the need for a normal variant in the patient sample, to be able to discriminate between the alleles in the distinction between partial or complete splicing aberration, and the assessment of biallelic expression in normal transcripts.
As the splicing process could be differently regulated in different tissues, a sample from breast or ovarian tissue would be ideal for the study of splicing variants in the breast cancer genes. This is usually not available in the clinical setting. However, ENIGMA concluded that BRCA1 alternative splicing is similar in blood and breast, supporting the clinical relevance of blood based in vitro splicing assays .
The methods used here were shown to work well and help in the functional assessment of several variants. However, there are numbers of potential splicing variants that we are missing because of lack of efficient ways of identifying these, such as variants affecting splicing enhancers and silencers. These and other regulatory variants will probably be better characterized in the near future.
We conclude that mRNA analyses are beneficial in characterization of variants that may affect splicing. The results can guide classification of variants from unknown clinical significance to pathogenic or benign, and thus be of great importance to patients and relatives, enabling female carriers to opt for disease screening and/or prevention. We characterized two novel pathogenic splicing variants. Development of knowledge and methods in the field will lead to identification and characterization of more splicing variants in the future.
Evidence-Based Network for the Interpretation of Germline Mutant Alleles
genome Aggregation Database
Nonsense-mediated mRNA decay
Reverse transcription polymerase chain reaction
Single nucleotide polymorphisms
Variant of unknown clinical significance
Breast cancer gene 1/2
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We are thankful to Oslo University Hospital and the Department of Medical genetics that enabled the performance of this quality of care study. We would like to thank everyone in the department who contributed to the work with laboratory methods and discussions of the results.
The work was done as part of a quality of care study at the Department of Medical Genetics, Oslo University Hospital, without extra funding.
Availability of data and materials
Primers are available upon request.
Ethics approval and consent to participate
The study was carried out in the Section of Laboratory Diagnostics at Department of Medical genetics, Oslo University Hospital, OUH. The study was assessed by the Data Protection Office at OUH and was approved by the Head of the Department of Medical genetics as a quality of care study.
Consent for publication
The authors declare that they have no competing interests.
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