Mutte Sumanth K, Barendse Patrick, Ugarte Pilar Bobadilla, Swarts Daan C
Laboratory of Biochemistry, Wageningen University, 6708 WE Wageningen, the Netherlands; MyGen Informatics, 6706 JE Wageningen, the Netherlands.
Laboratory of Biochemistry, Wageningen University, 6708 WE Wageningen, the Netherlands.
Cell Rep. 2025 Jan 28;44(1):115110. doi: 10.1016/j.celrep.2024.115110. Epub 2025 Jan 2.
Bacteria encode various DNA repair pathways to maintain genome integrity. However, the high degree of homology between DNA repair proteins or their domains hampers accurate identification. Here, we describe a stringent search strategy to identify DNA repair proteins and provide a systematic analysis of taxonomic distribution and co-occurrence of DNA repair proteins involved in RecA-dependent homologous recombination. Our results reveal the widespread presence of RecA, SSB, and RecOR proteins and phyla-specific distribution for the DNA repair complexes RecBCD, AddAB, and AdnAB. Furthermore, we report co-occurrences of DNA repair proteins with immune systems, including specific CRISPR-Cas subtypes, prokaryotic Argonautes (pAgos), dGTPases, GAPS2, and Wadjet. Our results imply that while certain DNA repair proteins and immune systems might function in conjunction, no immune system strictly relies on a specific DNA repair protein. As such, these findings offer an updated perspective on the distribution of DNA repair systems and their connection to immune systems in bacteria.
细菌编码多种DNA修复途径以维持基因组完整性。然而,DNA修复蛋白或其结构域之间的高度同源性阻碍了准确识别。在此,我们描述了一种严格的搜索策略来识别DNA修复蛋白,并对参与RecA依赖性同源重组的DNA修复蛋白的分类分布和共现情况进行系统分析。我们的结果揭示了RecA、单链结合蛋白(SSB)和RecOR蛋白的广泛存在,以及DNA修复复合物RecBCD、AddAB和AdnAB的门特异性分布。此外,我们报告了DNA修复蛋白与免疫系统的共现情况,包括特定的CRISPR-Cas亚型、原核生物的Argonaute蛋白(pAgos)、dGTP酶、GAPS2和Wadjet。我们的结果表明,虽然某些DNA修复蛋白和免疫系统可能协同发挥作用,但没有一种免疫系统严格依赖于特定的DNA修复蛋白。因此,这些发现为细菌中DNA修复系统的分布及其与免疫系统的联系提供了新的视角。