Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota Medical School, Minneapolis, MN, 55455, USA.
Department of Systems Biology, University of Texas, MD Anderson Cancer Center, Houston, TX, 77030.
DNA Repair (Amst). 2023 Feb;122:103445. doi: 10.1016/j.dnarep.2022.103445. Epub 2022 Dec 24.
Double-stranded breaks (DSBs) are toxic DNA damage and a serious threat to genomic integrity. Thus, all living organisms have evolved multiple mechanisms of DNA DSB repair, the two principal ones being classical-non homologous end joining (C-NHEJ), and homology dependent recombination (HDR). In mammals, C-NHEJ is the predominate DSB repair pathway, but how a cell chooses to repair a particular DSB by a certain pathway is still not mechanistically clear. To uncover novel regulators of DSB repair pathway choice, we performed a kinome-wide screen in a human cell line engineered to express a dominant-negative C-NHEJ factor. The intellectual basis for such a screen was our hypothesis that a C-NHEJ-crippled cell line might need to upregulate other DSB repair pathways, including HDR, in order to survive. This screen identified Bromodomain-containing Protein 3 (BRD3) as a protein whose expression was almost completely ablated specifically in a C-NHEJ-defective cell line. Subsequent experimentation demonstrated that BRD3 is a negative regulator of HDR as BRD3-null cell lines proved to be hyper-recombinogenic for gene conversion, sister chromatid exchanges and gene targeting. Mechanistically, BRD3 appears to be working at the level of Radiation Sensitive 51 (RAD51) recruitment. Overall, our results demonstrate that BRD3 is a novel regulator of human DSB repair pathway choice.
双链断裂 (DSBs) 是一种有毒的 DNA 损伤,对基因组的完整性构成严重威胁。因此,所有生物都进化出了多种 DNA DSB 修复机制,其中两种主要的机制是经典非同源末端连接 (C-NHEJ) 和同源依赖性重组 (HDR)。在哺乳动物中,C-NHEJ 是主要的 DSB 修复途径,但细胞如何选择通过特定途径修复特定的 DSB 在机制上尚不清楚。为了揭示 DSB 修复途径选择的新调控因子,我们在一种经过工程改造的人细胞系中进行了全激酶组筛选,该细胞系表达了一种显性负 C-NHEJ 因子。进行这种筛选的理论基础是我们的假设,即 C-NHEJ 受损的细胞系可能需要上调其他 DSB 修复途径,包括 HDR,以维持生存。该筛选鉴定出溴结构域蛋白 3 (BRD3) 作为一种蛋白质,其表达在 C-NHEJ 缺陷细胞系中几乎完全被消除。随后的实验表明,BRD3 是 HDR 的负调控因子,因为 BRD3 缺失细胞系在基因转换、姐妹染色单体交换和基因靶向方面表现出高度的重组能力。从机制上讲,BRD3 似乎作用于辐射敏感 51 (RAD51) 募集水平。总的来说,我们的结果表明 BRD3 是人类 DSB 修复途径选择的一种新调控因子。