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Expression of human BRCA2 in Saccharomyces cerevisiae complements the loss of RAD52 in double-strand break repair
Current Genetics ( IF 2.5 ) Pub Date : 2023-11-07 , DOI: 10.1007/s00294-023-01278-y
Sherrice Law 1 , Hannah Park 1 , Eyar Shany 2 , Sumer Sandhu 3 , Mayukha Vallabhaneni 4 , Damon Meyer 4
Affiliation  

BRCA2 is a tumor-suppressor gene that is normally expressed in the breast and ovarian tissue of mammals. The BRCA2 protein mediates the repair of double-strand breaks (DSBs) using homologous recombination, which is a conserved pathway in eukaryotes. Women who express missense mutations in the BRCA2 gene are predisposed to an elevated lifetime risk for both breast cancer and ovarian cancer. In the present study, the efficiency of human BRCA2 (hBRCA2) in DSB repair was investigated in the budding yeast Saccharomyces cerevisiae. While budding yeast does not possess a true BRCA2 homolog, they have a potential functional homolog known as Rad52, which is an essential repair protein involved in mediating homologous recombination using the same mechanism as BRCA2 in humans. Therefore, to examine the functional overlap between Rad52 in yeast and hBRCA2, we expressed the wild-type hBRCA2 gene in budding yeast with or without Rad52 and monitored ionizing radiation resistance and DSB repair efficiency. We found that the expression of hBRCA2 in rad52 mutants increases both radiation resistance and DSB repair frequency compared to cells not expressing BRCA2. Specifically, BRCA2 improved the protection against ionizing radiation by at least 1.93-fold and the repair frequency by 6.1-fold. In addition, our results show that homology length influences repair efficiency in rad52 mutant cells, which impacts BRCA2 mediated repair of DSBs. This study provides evidence that S. cerevisiae could be used to monitor BRCA2 function, which can help in understanding the genetic consequences of BRCA2 variants and how they may contribute to cancer progression.



中文翻译:

人类 BRCA2 在酿酒酵母中的表达补充了双链断裂修复中 RAD52 的缺失

BRCA2是一种肿瘤抑制基因,通常在哺乳动物的乳腺和卵巢组织中表达。BRCA2 蛋白利用同源重组介导双链断裂 (DSB) 修复,这是真核生物中的保守途径。BRCA2基因表达错义突变的女性一生中罹患乳腺癌和卵巢癌的风险较高。在本研究中,在芽殖酵母酿酒酵母中研究了人类 BRCA2 (hBRCA2) 在 DSB 修复中的效率。虽然芽殖酵母不具有真正的 BRCA2 同源物,但它们具有潜在的功能同源物,称为 Rad52,这是一种重要的修复蛋白,参与介导同源重组,其机制与人类 BRCA2 相同。因此,为了检查酵母中 Rad52 和 hBRCA2 之间的功能重叠,我们在有或没有 Rad52 的芽殖酵母中表达野生型hBRCA2基因,并监测电离辐射抗性和 DSB 修复效率。我们发现,与不表达 BRCA2 的细胞相比,rad52突变体中hBRCA2的表达增加了辐射抗性和 DSB 修复频率。具体来说,BRCA2 将电离辐射防护提高了至少 1.93 倍,修复频率提高了 6.1 倍。此外,我们的结果表明,同源长度影响rad52突变细胞的修复效率,从而影响 BRCA2 介导的 DSB 修复。这项研究提供了酿酒酵母可用于监测 BRCA2 功能的证据,这有助于了解 BRCA2 变异的遗传后果以及它们如何促进癌症进展。

更新日期:2023-11-09
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