Localization of MMR proteins on meiotic chromosomes in mice indicates distinct functions during prophase I
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hMSH4-hMSH5 adenosine nucleotide processing and interactions with homologous recombination machineryConditional inactivation of the DNA damage response gene Hus1 in mouse testis reveals separable roles for components of the RAD9-RAD1-HUS1 complex in meiotic chromosome maintenanceMammalian BTBD12 (SLX4) protects against genomic instability during mammalian spermatogenesisNew insights into the mechanism of DNA mismatch repairVariation in crossover frequencies perturb crossover assurance without affecting meiotic chromosome segregation in Saccharomyces cerevisiaeMlh1-Mlh3, a meiotic crossover and DNA mismatch repair factor, is a Msh2-Msh3-stimulated endonucleaseThe Saccharomyces cerevisiae Mlh1-Mlh3 heterodimer is an endonuclease that preferentially binds to Holliday junctions.AGO4 regulates entry into meiosis and influences silencing of sex chromosomes in the male mouse germlineRNF212 is a dosage-sensitive regulator of crossing-over during mammalian meiosisDeletion of genes implicated in protecting the integrity of male germ cells has differential effects on the incidence of DNA breaks and germ cell lossFancJ (Brip1) loss-of-function allele results in spermatogonial cell depletion during embryogenesis and altered processing of crossover sites during meiotic prophase I in miceMammalian CNTD1 is critical for meiotic crossover maturation and deselection of excess precrossover sitesEvolutionary rate covariation in meiotic proteins results from fluctuating evolutionary pressure in yeasts and mammalsTwo levels of interference in mouse meiotic recombinationMUS81 generates a subset of MLH1-MLH3-independent crossovers in mammalian meiosis.MSH2 ATPase domain mutation affects CTG*CAG repeat instability in transgenic mice.Modulating Crossover Frequency and Interference for Obligate Crossovers in Saccharomyces cerevisiae Meiosis.Genetic analysis of baker's yeast Msh4-Msh5 reveals a threshold crossover level for meiotic viability.Mammalian BLM helicase is critical for integrating multiple pathways of meiotic recombinationPMS2 endonuclease activity has distinct biological functions and is essential for genome maintenance.Evidence that hMLH3 functions primarily in meiosis and in hMSH2-hMSH3 mismatch repair.Senataxin plays an essential role with DNA damage response proteins in meiotic recombination and gene silencingMismatch repair during homologous and homeologous recombinationNEK1 Facilitates Cohesin Removal during Mammalian SpermatogenesisMlh1 deficiency in zebrafish results in male sterility and aneuploid as well as triploid progeny in females.Dgcr8 and Dicer are essential for sex chromosome integrity during meiosis in males.The Arabidopsis HEI10 is a new ZMM protein related to Zip3Using crossover breakpoints in recombinant inbred lines to identify quantitative trait loci controlling the global recombination frequency.Meiosis-specific proteins MEIOB and SPATA22 cooperatively associate with the single-stranded DNA-binding replication protein A complex and DNA double-strand breaks.Distinct DNA-binding surfaces in the ATPase and linker domains of MutLγ determine its substrate specificities and exert separable functions in meiotic recombination and mismatch repairRoles for mismatch repair family proteins in promoting meiotic crossing over.Distinct functions of MLH3 at recombination hot spots in the mouse.An intact Pms2 ATPase domain is not essential for male fertilityDistinct effects of the recurrent Mlh1G67R mutation on MMR functions, cancer, and meiosisA mutation in the putative MLH3 endonuclease domain confers a defect in both mismatch repair and meiosis in Saccharomyces cerevisiae.Ubiquitylated PCNA plays a role in somatic hypermutation and class-switch recombination and is required for meiotic progression.Reassessment of the role of Mut S homolog 5 in Ig class switch recombination shows lack of involvement in cis- and trans-switching.Proteins involved in meiotic recombination: a role in male infertility?Structural insights into Saccharomyces cerevisiae Msh4-Msh5 complex function using homology modelingStable expression of MutLγ in human cells reveals no specific response to mismatched DNA, but distinct recruitment to damage sites.
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P2860
Localization of MMR proteins on meiotic chromosomes in mice indicates distinct functions during prophase I
description
2005 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2005
@ast
im November 2005 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2005/11/07)
@sk
vědecký článek publikovaný v roce 2005
@cs
wetenschappelijk artikel (gepubliceerd op 2005/11/07)
@nl
наукова стаття, опублікована в листопаді 2005
@uk
مقالة علمية (نشرت في 7-11-2005)
@ar
name
Localization of MMR proteins o ...... ct functions during prophase I
@ast
Localization of MMR proteins o ...... ct functions during prophase I
@en
Localization of MMR proteins o ...... ct functions during prophase I
@nl
type
label
Localization of MMR proteins o ...... ct functions during prophase I
@ast
Localization of MMR proteins o ...... ct functions during prophase I
@en
Localization of MMR proteins o ...... ct functions during prophase I
@nl
prefLabel
Localization of MMR proteins o ...... ct functions during prophase I
@ast
Localization of MMR proteins o ...... ct functions during prophase I
@en
Localization of MMR proteins o ...... ct functions during prophase I
@nl
P2093
P2860
P921
P356
P1476
Localization of MMR proteins o ...... ct functions during prophase I
@en
P2093
Anton Svetlanov
Frank P. Macaluso
John Greally
Michelle L. Lenzi
Nadine K. Kolas
Paula E. Cohen
R. Michael Liskay
Steven M. Lipkin
Winfried Edelmann
P2860
P304
P356
10.1083/JCB.200506170
P407
P577
2005-11-07T00:00:00Z