Litcius/Paper detail

A conserved Ctp1/CtIP C-terminal peptide stimulates Mre11 endonuclease activity

Aleksandar Zdravković, James M. Daley, Arijit Dutta, Tatsuya Niwa, Yasuto Murayama, Shuji Kanamaru, Kentaro Ito, Takahisa Maki, Bilge Argunhan, Masayuki Takahashi, Hideo Tsubouchi, Patrick Sung, Hiroshi Iwasaki

2021Proceedings of the National Academy of Sciences22 citationsDOIOpen Access PDF

Abstract

homolog of human CtIP. Here, with purified proteins, we show that Ctp1 phosphorylation stimulates MRN endonuclease activity by inducing the association of Ctp1 with Nbs1. The highly conserved extreme C terminus of Ctp1 is indispensable for MRN activation. Importantly, a polypeptide composed of the conserved 15 amino acids at the C terminus of Ctp1 (CT15) is sufficient to stimulate Mre11 endonuclease activity. Furthermore, the CT15 equivalent from CtIP can stimulate human MRE11 endonuclease activity, arguing for the generality of this stimulatory mechanism. Thus, we propose that Nbs1-mediated recruitment of CT15 plays a pivotal role in the activation of the Mre11 endonuclease by Ctp1/CtIP.

Topics & Concepts

EndonucleasePeptideBiologyCell biologyMolecular biologyChemistryGeneticsDNABiochemistryRNA modifications and cancerCRISPR and Genetic EngineeringChromosomal and Genetic Variations
A conserved Ctp1/CtIP C-terminal peptide stimulates Mre11 endonuclease activity | Litcius