Functional Characterization of the Human BRCA1 △11 Splicing Isoforms in Yeast

被引:0
|
作者
Galli, Alvaro [1 ]
Belle, Francesca [1 ]
Fargnoli, Arcangelo [1 ]
Caligo, Maria Adelaide [2 ]
Cervelli, Tiziana [1 ]
机构
[1] CNR, Inst Clin Physiol, Lab Funct Genet & Genom, Yeast Genet & Genom, I-56124 Pisa, Italy
[2] Univ Hosp Pisa, Dept Oncol, Mol Genet Unit, Pisa, Italy
关键词
BRCA1 triangle 11 splicing isoforms; yeast-based functional assay; BRCA1 intronic variants; BRCA1; localization; SUBCELLULAR-LOCALIZATION; SEQUENCE VARIANTS; MURINE BRCA1; EXPRESSION; RECOMBINATION; ASSOCIATION; BRCA1-DELTA-11; RESISTANCE; MUTATIONS; GENOMICS;
D O I
10.3390/ijms25147511
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
BRCA1, a crucial tumor suppressor gene, has several splicing isoforms, including Delta 9-11, Delta 11, and Delta 11q, which lack exon 11, coding for significant portions of the protein. These isoforms are naturally present in both normal and cancerous cells, exhibiting altered activity compared to the full-length BRCA1. Despite this, the impact on cancer risk of the germline intronic variants promoting the exclusive expression of these Delta 11 isoforms remains uncertain. Consequently, they are classified as variants of uncertain significance (VUS), posing challenges for traditional genetic classification methods due to their rarity and complexity. Our research utilizes a yeast-based functional assay, previously validated for assessing missense BRCA1 variants, to compare the activity of the Delta 11 splicing isoforms with known pathogenic missense variants. This approach allows us to elucidate the functional implications of these isoforms and determine whether their exclusive expression could contribute to increased cancer risk. By doing so, we aim to provide insights into the pathogenic potential of intronic VUS-generating BRCA1 splicing isoforms and improve the classification of BRCA1 variants.
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页数:12
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