Literature DB >> 22749142

The functions of MutL in mismatch repair: the power of multitasking.

Alba Guarné1.   

Abstract

DNA mismatch repair enhances genomic stability by correcting errors that have escaped polymerase proofreading. One of the critical steps in DNA mismatch repair is discriminating the new from the parental DNA strand as only the former needs repair. In Escherichia coli, the latent endonuclease MutH carries out this function. However, most prokaryotes and all eukaryotes lack a mutH gene. MutL is a key component of this system that mediates protein-protein interactions during mismatch recognition, strand discrimination, and strand removal. Hence, it had long been thought that the primary function of MutL was coordinating sequential mismatch repair steps. However, recent studies have revealed that most MutL homologs from organisms lacking MutH encode a conserved metal-binding motif associated with a weak endonuclease activity. As MutL homologs bearing this activity are found only in organisms relying on MutH-independent DNA mismatch repair, this finding unveils yet another crucial function of the MutL protein at the strand discrimination step. In this chapter, we review recent functional and structural work aimed at characterizing the multiple functions of MutL and discuss how the endonuclease activity of MutL is regulated by other repair factors.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22749142     DOI: 10.1016/B978-0-12-387665-2.00003-1

Source DB:  PubMed          Journal:  Prog Mol Biol Transl Sci        ISSN: 1877-1173            Impact factor:   3.622


  21 in total

1.  Mlh1-Mlh3, a meiotic crossover and DNA mismatch repair factor, is a Msh2-Msh3-stimulated endonuclease.

Authors:  Maria V Rogacheva; Carol M Manhart; Cheng Chen; Alba Guarne; Jennifer Surtees; Eric Alani
Journal:  J Biol Chem       Date:  2014-01-08       Impact factor: 5.157

Review 2.  Modifiers of CAG/CTG Repeat Instability: Insights from Mammalian Models.

Authors:  Vanessa C Wheeler; Vincent Dion
Journal:  J Huntingtons Dis       Date:  2021

Review 3.  Postreplicative mismatch repair.

Authors:  Josef Jiricny
Journal:  Cold Spring Harb Perspect Biol       Date:  2013-04-01       Impact factor: 10.005

4.  The Saccharomyces cerevisiae Mlh1-Mlh3 heterodimer is an endonuclease that preferentially binds to Holliday junctions.

Authors:  Lepakshi Ranjha; Roopesh Anand; Petr Cejka
Journal:  J Biol Chem       Date:  2014-01-17       Impact factor: 5.157

Review 5.  The changing landscape of Lynch syndrome due to PMS2 mutations.

Authors:  J Blount; A Prakash
Journal:  Clin Genet       Date:  2018-03-15       Impact factor: 4.438

6.  Biochemical and structural characterization of two variants of uncertain significance in the PMS2 gene.

Authors:  Brandon M D'Arcy; Jessa Blount; Aishwarya Prakash
Journal:  Hum Mutat       Date:  2019-01-30       Impact factor: 4.878

Review 7.  New insights into the mechanism of DNA mismatch repair.

Authors:  Gloria X Reyes; Tobias T Schmidt; Richard D Kolodner; Hans Hombauer
Journal:  Chromosoma       Date:  2015-04-11       Impact factor: 4.316

8.  Dual daughter strand incision is processive and increases the efficiency of DNA mismatch repair.

Authors:  Nicolaas Hermans; Charlie Laffeber; Michele Cristovão; Mariela Artola-Borán; Yannicka Mardenborough; Pauline Ikpa; Aruna Jaddoe; Herrie H K Winterwerp; Claire Wyman; Josef Jiricny; Roland Kanaar; Peter Friedhoff; Joyce H G Lebbink
Journal:  Nucleic Acids Res       Date:  2016-05-12       Impact factor: 16.971

Review 9.  Roles for mismatch repair family proteins in promoting meiotic crossing over.

Authors:  Carol M Manhart; Eric Alani
Journal:  DNA Repair (Amst)       Date:  2015-12-02

10.  Structural Features and Functional Dependency on β-Clamp Define Distinct Subfamilies of Bacterial Mismatch Repair Endonuclease MutL.

Authors:  Kenji Fukui; Seiki Baba; Takashi Kumasaka; Takato Yano
Journal:  J Biol Chem       Date:  2016-07-01       Impact factor: 5.157

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