基因编辑权威指南。
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基因 · Cancer

BRCA1

BRCA1 DNA repair associated · A DNA repair gene whose loss substantially raises the risk of breast and ovarian cancer, important to gene editing mostly because of the repair pathway it serves.

17q21.31 cancerDNA repair
染色体 17 BRCA1 17q21.31 p q

仅为示意图——染色体臂比例为近似值,条带细节未按比例绘制。细胞遗传学位置以 NCBI Gene 公布的数据为准。

这个基因的功能

BRCA1 helps repair a specific kind of DNA damage: breaks through both strands. Inherit a broken copy and your cells repair such damage less well, and cancer risk rises substantially. It matters to gene editing for a reason people find surprising: the repair pathway BRCA1 works in is the same one CRISPR relies on when it makes a precise correction.

BRCA1, at 17q21.31, encodes a tumour suppressor central to homologous recombination repair of double-strand breaks. Pathogenic variants confer substantially elevated lifetime risk of breast and ovarian cancer. Its relevance to editing is mechanistic: homology-directed repair, the pathway required for template-based correction after a Cas9 cut, is the pathway BRCA1 serves, and it operates only in dividing cells, which is a fundamental constraint on precise editing.

Sources

  • MedlinePlus Genetics, U.S. National Library of Medicine
    BRCA1 gene ↗

Connected in CRISPR Decoded

Every entry on this site is linked to the others it relates to. These connections are part of the record, not a search result.

Diseases

Cancer