School of Life Sciences, University of Nottingham, Nottingham NG7 2UH, UK.
Centre for Medicines Discovery, University of Oxford, Oxford OX3 7FZ, UK.
Int J Mol Sci. 2024 Nov 19;25(22):12417. doi: 10.3390/ijms252212417.
Multiple modes of DNA repair need DNA synthesis by DNA polymerase enzymes. The eukaryotic B-family DNA polymerase complexes delta (Polδ) and zeta (Polζ) help to repair DNA strand breaks when primed by homologous recombination or single-strand DNA annealing. DNA synthesis by Polδ and Polζ is mutagenic, but is needed for the survival of cells in the presence of DNA strand breaks. The POLD3 subunit of Polδ and Polζ is at the heart of DNA repair by recombination, by modulating polymerase functions and interacting with other DNA repair proteins. We provide the background to POLD3 discovery, investigate its structure, as well as function in cells. We highlight unexplored structural aspects of POLD3 and new biochemical data that will help to understand the pivotal role of POLD3 in DNA repair and mutagenesis in eukaryotes, and its impact on human health.
多种 DNA 修复模式需要 DNA 聚合酶酶来进行 DNA 合成。真核生物 B 族 DNA 聚合酶复合物 delta(Polδ)和 zeta(Polζ)在同源重组或单链 DNA 退火引发时有助于修复 DNA 链断裂。Polδ 和 Polζ 的 DNA 合成具有诱变作用,但对于在 DNA 链断裂存在的情况下细胞的存活是必需的。Polδ 和 Polζ 的 POLD3 亚基是通过重组进行 DNA 修复的核心,通过调节聚合酶功能并与其他 DNA 修复蛋白相互作用。我们提供了 POLD3 发现的背景,研究了它的结构,以及在细胞中的功能。我们强调了 POLD3 未被探索的结构方面和新的生化数据,这些将有助于理解 POLD3 在真核生物中 DNA 修复和诱变中的关键作用,以及它对人类健康的影响。