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<dc:title>Unraveling the molecular effect of a rare missense mutation in BRIP1 associated with inherited breast cancer</dc:title>
<dc:creator>Velázquez Pérez, Carolina</dc:creator>
<dc:creator>Esteban Cardeñosa, Eva</dc:creator>
<dc:creator>Lastra, Enrique</dc:creator>
<dc:creator>Abella, Luis Enrique</dc:creator>
<dc:creator>de la Cruz, Virginia</dc:creator>
<dc:creator>Domínguez Lobatón, María Carmen</dc:creator>
<dc:creator>Duran Dominguez, María Mercedes</dc:creator>
<dc:creator>Infante Sanz, María Del Mar</dc:creator>
<dc:description>BRIP1 is a component of the Fanconi Anemia/BRCA pathway responsible for DNA reparation via helicase activity. Some heterozygous variants in BRIP1 could contribute to Hereditary Breast Cancer through a defective DNA repair. The clinical utility of BRIP1 mutations in a familial cancer context is compromised by the conflicting interpretation of “variants of uncertain significance” (VUS). Defining the clinical significance of variants identified in genetic tests is a major challenge; therefore, studies that evaluate the biological effect of these variants are definitely necessary. To contribute to this purpose, we have characterized the variant c.550G>T of BRIP1, a missense mutation with little evidence about its pathogenicity. Since Human Splicing FinderTM predicts the creation of a new exonic splicing enhancer site we decided to perform cDNA analysis revealing that the c.550G>T mutation located in exon 6 led to an aberrant transcript causing exon 5 skipping. Our results demonstrate that the c.550G>T BRIP1 variant disrupts normal splicing, causing exon 5 skipping. Considering that the exon 5 encodes the helicase domain of BRIP1, it is expected an alteration of the function. This finding enhances the interpretation of this VUS, suggesting a potential pathogenic effect.</dc:description>
<dc:date>2025-01-09T11:10:17Z</dc:date>
<dc:date>2025-01-09T11:10:17Z</dc:date>
<dc:date>2019</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:type>info:eu-repo/semantics/draft</dc:type>
<dc:identifier>Molecular Carcinogenesis,2019 Jan;58(1):156-160</dc:identifier>
<dc:identifier>0899-1987</dc:identifier>
<dc:identifier>https://uvadoc.uva.es/handle/10324/73281</dc:identifier>
<dc:identifier>10.1002/mc.22910</dc:identifier>
<dc:identifier>156</dc:identifier>
<dc:identifier>1</dc:identifier>
<dc:identifier>160</dc:identifier>
<dc:identifier>Molecular Carcinogenesis</dc:identifier>
<dc:identifier>58</dc:identifier>
<dc:identifier>1098-2744</dc:identifier>
<dc:language>spa</dc:language>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:format>application/pdf</dc:format>
<dc:publisher>Wiley</dc:publisher>
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