Literature DB >> 9299235

Cloning and expression analysis of a meiosis-specific MutS homolog: the human MSH4 gene.

V Paquis-Flucklinger1, S Santucci-Darmanin, R Paul, A Saunières, C Turc-Carel, C Desnuelle.   

Abstract

The Escherichia coli MutHLS system has been highly conserved throughout evolution. The eukaryotic pathway results in a specialization of MutS homologs that have evolved to play crucial roles in both DNA mismatch repair and meiotic recombination. So far, meiosis-specific genes belonging to this family have only been identified in yeast. In Saccharomyces cerevisiae, MSH4 (MutS homolog 4) is a meiosis-specific protein that is not involved in mismatch correction. This protein is required for reciprocal recombination and proper segregation of homologous chromosomes at meiosis I. We have identified the human MSH4 homolog gene. The predicted amino acid sequence shows 28.7% identity with the S. cerevisiae MSH4 protein. By Northern blot analysis, human MSH4 transcripts are only detectable in testis and in ovary with a lower level of expression. We have mapped MSH4 to human chromosome 1 at band p31 by fluorescence in situ hybridization. The identification of such a gene provides a powerful tool for clarifying the respective roles of MSH and MLH genes in mammalian meiosis. Copyright 1997 Academic Press.

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Year:  1997        PMID: 9299235     DOI: 10.1006/geno.1997.4857

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  26 in total

Review 1.  Regulating double-stranded DNA break repair towards crossover or non-crossover during mammalian meiosis.

Authors:  Frédéric Baudat; Bernard de Massy
Journal:  Chromosome Res       Date:  2007       Impact factor: 5.239

2.  hMSH5 is a nucleocytoplasmic shuttling protein whose stability depends on its subcellular localization.

Authors:  François Lahaye; Françoise Lespinasse; Pascal Staccini; Lucile Palin; Véronique Paquis-Flucklinger; Sabine Santucci-Darmanin
Journal:  Nucleic Acids Res       Date:  2010-02-25       Impact factor: 16.971

3.  MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice.

Authors:  B Kneitz; P E Cohen; E Avdievich; L Zhu; M F Kane; H Hou; R D Kolodner; R Kucherlapati; J W Pollard; W Edelmann
Journal:  Genes Dev       Date:  2000-05-01       Impact factor: 11.361

4.  Crossing over during Caenorhabditis elegans meiosis requires a conserved MutS-based pathway that is partially dispensable in budding yeast.

Authors:  J Zalevsky; A J MacQueen; J B Duffy; K J Kemphues; A M Villeneuve
Journal:  Genetics       Date:  1999-11       Impact factor: 4.562

Review 5.  Lynch syndrome genes.

Authors:  Päivi Peltomäki
Journal:  Fam Cancer       Date:  2005       Impact factor: 2.375

6.  The interacting domains of three MutL heterodimers in man: hMLH1 interacts with 36 homologous amino acid residues within hMLH3, hPMS1 and hPMS2.

Authors:  E Kondo; A Horii; S Fukushige
Journal:  Nucleic Acids Res       Date:  2001-04-15       Impact factor: 16.971

7.  A phylogenomic study of the MutS family of proteins.

Authors:  J A Eisen
Journal:  Nucleic Acids Res       Date:  1998-09-15       Impact factor: 16.971

8.  RACE using only a gene-specific primer: application of a template-switching model.

Authors:  Masanori Hirano
Journal:  Mol Biotechnol       Date:  2004-07       Impact factor: 2.695

9.  Mammalian BLM helicase is critical for integrating multiple pathways of meiotic recombination.

Authors:  J Kim Holloway; Meisha A Morelli; Peter L Borst; Paula E Cohen
Journal:  J Cell Biol       Date:  2010-03-22       Impact factor: 10.539

10.  VBP1 facilitates proteasome and autophagy-mediated degradation of MutS homologue hMSH4.

Authors:  Yang Xu; Chengtao Her
Journal:  FASEB J       Date:  2013-08-20       Impact factor: 5.191

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