hMSH5: A human MutS homologue that forms a novel heterodimer with hMSH4 and is expressed during spermatogenesis

Tina Bocker, Alan Barusevicius, Tim Snowden, Debora Rasio, Shawn Guerrette, David Robbins, Carl Schmidt, John Burczak, Carlo M. Croce, Terry Copeland, Albert J. Kovatich, Richard Fishel*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

87 Scopus citations

Abstract

MutS homologues have been identified in nearly all organisms examined to date. They play essential roles in maintaining mitotic genetic fidelity and meiotic segregation fidelity. MutS homologues appear to function as a molecular switch that signals genomic manipulation events. Here we describe the identification of the human homologue of the Saccharomyces cerevisiae MSH5, which is known to participate in meiotic segregation fidelity and crossing-over. The human MSH5 (hMSH5) was localized to chromosome 6p22-21 and appears to play a role in meiosis because expression is induced during spermatogenesis between the late primary spermatocytes and the elongated spermatid phase. hMSH5 interacts specifically with hMSH4, confirming the generality of functional heterodimeric interactions in the eukaryotic MutS homologue, which also includes hMSH2-hMSH3 and hMSH2-hMSH6.

Original languageEnglish
Pages (from-to)816-822
Number of pages7
JournalCancer Research
Volume59
Issue number4
StatePublished - 15 Feb 1999
Externally publishedYes

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