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

  1. Author:
    Bocher, T.
    Barusevicius, A.
    Snowden, T.
    Rasio, D.
    Guerrette, S.
    Robbins, D.
    Schmidt, C.
    Burczak, J.
    Croce, C. M.
    Copeland, T.
    Kovatich, A. J.
    Fishel, R.
  2. Author Address

    Fishel R Thomas Jefferson Univ, Jefferson Med Coll, Kimmel Canc Inst, Dept Microbiol & Immunol 233 S 10th St Philadelphia, PA 19107 USA Thomas Jefferson Univ, Jefferson Med Coll, Kimmel Canc Inst, Dept Microbiol & Immunol Philadelphia, PA 19107 USA Thomas Jefferson Univ, Jefferson Med Coll, Kimmel Canc Inst, Dept Pathol & Cell Biol Philadelphia, PA 19107 USA SmithKline Beecham Pharmaceut King Of Prussia, PA 19406 USA NCI, Frederick Canc Res & Dev Ctr, ABL Basic Res Program Frederick, MD 21702 USA
    1. Year: 1999
  1. Journal: Cancer Research
    1. 59
    2. 4
    3. Pages: 816-822
  2. Type of Article: Article
  1. 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. [References: 25]

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