Piscitelli Jonathan M, Witte Scott J, Sakinejad Yasmine S, Manhart Carol M
Department of Chemistry, Temple University, 1901 N. 13th St. Philadelphia, PA 19122, USA.
Nucleic Acids Res. 2025 Jan 24;53(3). doi: 10.1093/nar/gkae1253.
In eukaryotic post-replicative mismatch repair, MutS homolog complexes detect mismatches and in the major eukaryotic pathway, recruit Mlh1-Pms1/MLH1-PMS2 (yeast/human) complexes, which nick the newly replicated DNA strand upon activation by the replication processivity clamp, PCNA. This incision enables mismatch removal and DNA repair. Beyond its endonuclease role, Mlh1-Pms1/MLH1-PMS2 also has ATPase activity, which genetic studies suggest is essential for mismatch repair, although its precise regulatory role on DNA remains unclear. Here, we use an ATP-binding and hydrolysis-deficient yeast Mlh1-Pms1 variant to show that ATP hydrolysis promotes disengagement from Mlh1-Pms1-generated nicks, with hydrolysis in the Mlh1 subunit driving this activity. Our data suggest that the ATPase-deficient variant becomes trapped on its own endonuclease product, suggesting a mechanistic explanation for observations in genetic experiments. Additionally, we observed that Mlh1-Pms1 selectively protects DNA from exonuclease degradation at pre-existing nicks, which may act as strand discrimination signals in mismatch repair. Together, our findings suggest that Mlh1-Pms1 exhibits distinct behaviors on its own endonuclease products versus substrates with pre-existing nicks, supporting two distinct modes of action during DNA mismatch repair.
在真核生物复制后错配修复过程中,MutS同源复合物可检测到错配,并且在主要的真核生物途径中,招募Mlh1 - Pms1 / MLH1 - PMS2(酵母/人类)复合物,该复合物在被复制持续性钳PCNA激活后,会切割新复制的DNA链。这种切割使得错配得以去除并进行DNA修复。除了其核酸内切酶作用外,Mlh1 - Pms1 / MLH1 - PMS2还具有ATP酶活性,遗传学研究表明该活性对错配修复至关重要,尽管其对DNA的确切调控作用仍不清楚。在此,我们使用一种ATP结合和水解缺陷的酵母Mlh1 - Pms1变体来表明,ATP水解促进了与Mlh1 - Pms1产生的切口的脱离,Mlh1亚基中的水解驱动了这种活性。我们的数据表明,ATP酶缺陷变体被困在其自身的核酸内切酶产物上,这为遗传学实验中的观察结果提供了一种机制解释。此外,我们观察到Mlh1 - Pms1在预先存在的切口处选择性地保护DNA免受核酸外切酶降解,这可能在错配修复中作为链区分信号。总之,我们的研究结果表明,Mlh1 - Pms1在其自身的核酸内切酶产物与预先存在切口的底物上表现出不同的行为,支持了DNA错配修复过程中的两种不同作用模式。