Arora Sucheta, Deshpande Rajashree A, Budd Martin, Campbell Judy, Revere America, Zhang Xiaoming, Schmidt Kristina H, Paull Tanya T
The Howard Hughes Medical Institute, Department of Molecular Biosciences, and Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, Texas, USA.
Braun Laboratories, California Institute of Technology, Pasadena, California, USA.
Mol Cell Biol. 2017 Nov 28;37(24). doi: 10.1128/MCB.00156-17. Print 2017 Dec 15.
Sae2 promotes the repair of DNA double-strand breaks in The role of Sae2 is linked to the Mre11/Rad50/Xrs2 (MRX) complex, which is important for the processing of DNA ends into single-stranded substrates for homologous recombination. Sae2 has intrinsic endonuclease activity, but the role of this activity has not been assessed independently from its functions in promoting Mre11 nuclease activity. Here we identify and characterize separation-of-function mutants that lack intrinsic nuclease activity or the ability to promote Mre11 endonucleolytic activity. We find that the ability of Sae2 to promote MRX nuclease functions is important for DNA damage survival, particularly in the absence of Dna2 nuclease activity. In contrast, Sae2 nuclease activity is essential for DNA repair when the Mre11 nuclease is compromised. Resection of DNA breaks is impaired when either Sae2 activity is blocked, suggesting roles for both Mre11 and Sae2 nuclease activities in promoting the processing of DNA ends Finally, both activities of Sae2 are important for sporulation, indicating that the processing of meiotic breaks requires both Mre11 and Sae2 nuclease activities.
Sae2促进DNA双链断裂的修复。Sae2的作用与Mre11/Rad50/Xrs2(MRX)复合物相关,该复合物对于将DNA末端加工成用于同源重组的单链底物很重要。Sae2具有内在的核酸内切酶活性,但其活性的作用尚未与其促进Mre11核酸酶活性的功能分开评估。在这里,我们鉴定并表征了缺乏内在核酸酶活性或促进Mre11核酸内切酶活性能力的功能分离突变体。我们发现,Sae2促进MRX核酸酶功能的能力对于DNA损伤存活很重要,特别是在缺乏Dna2核酸酶活性的情况下。相比之下,当Mre11核酸酶受损时,Sae2核酸酶活性对于DNA修复至关重要。当Sae2活性被阻断时,DNA断裂的切除受损,这表明Mre11和Sae2核酸酶活性在促进DNA末端加工中都发挥作用。最后,Sae2的两种活性对于孢子形成都很重要,这表明减数分裂断裂的加工需要Mre11和Sae2核酸酶活性。