Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario L8N 3Z5, Canada.
Nucleic Acids Res. 2012 Mar;40(5):2131-9. doi: 10.1093/nar/gkr1059. Epub 2011 Nov 18.
Many types of DNA structures are generated in response to DNA damage, repair and recombination that require processing via specialized nucleases. DNA hairpins represent one such class of structures formed during V(D)J recombination, palindrome extrusion, DNA transposition and some types of double-strand breaks. Here we present biochemical and genetic evidence to suggest that Pso2 is a robust DNA hairpin opening nuclease in budding yeast. Pso2 (SNM1A in mammals) belongs to a small group of proteins thought to function predominantly during interstrand crosslink (ICL) repair. In this study, we characterized the nuclease activity of Pso2 toward a variety of DNA substrates. Unexpectedly, Pso2 was found to be an efficient, structure-specific DNA hairpin opening endonuclease. This activity was further shown to be required in vivo for repair of chromosomal breaks harboring closed hairpin ends. These findings provide the first evidence that Pso2 may function outside ICL repair and open the possibility that Pso2 may function at least in part during ICL repair by processing DNA intermediates including DNA hairpins or hairpin-like structures.
许多类型的 DNA 结构是在应对 DNA 损伤、修复和重组时产生的,这些过程需要通过专门的核酸酶进行处理。发夹结构是在 V(D)J 重组、回文序列外突、DNA 转座和某些类型的双链断裂过程中形成的一类结构。本文通过生化和遗传证据表明,Pso2 是一种在 budding yeast 中具有强大发夹结构打开活性的核酸内切酶。Pso2(哺乳动物中的 SNM1A)属于一小类蛋白,被认为主要在链间交联(ICL)修复中发挥作用。在本研究中,我们对 Pso2 对各种 DNA 底物的核酸酶活性进行了表征。出乎意料的是,发现 Pso2 是一种高效、结构特异性的 DNA 发夹结构内切酶。体内实验进一步表明,该活性对于修复含有闭合发夹末端的染色体断裂是必需的。这些发现首次证明 Pso2 可能在 ICL 修复之外发挥作用,并为 Pso2 可能通过处理包括 DNA 发夹或发夹样结构在内的 DNA 中间体来参与 ICL 修复提供了可能性。