Bocker 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
Department of Microbiology and Immunology, Kimmel Cancer Institute, Thomas Jefferson University and Medical College, Philadelphia, Pennsylvania 19107, USA.
Cancer Res. 1999 Feb 15;59(4):816-22.
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.
到目前为止,几乎在所有已检测的生物体中都发现了MutS同源物。它们在维持有丝分裂遗传保真度和减数分裂分离保真度方面发挥着重要作用。MutS同源物似乎起着分子开关的作用,对基因组操作事件发出信号。在此,我们描述了酿酒酵母MSH5的人类同源物的鉴定,已知该同源物参与减数分裂分离保真度和交叉互换。人类MSH5(hMSH5)定位于6号染色体p22 - 21区域,并且似乎在减数分裂中发挥作用,因为在初级精母细胞后期和延长的精子细胞阶段之间的精子发生过程中其表达被诱导。hMSH5与hMSH4特异性相互作用,证实了真核生物MutS同源物中功能性异源二聚体相互作用的普遍性,其中还包括hMSH2 - hMSH3和hMSH2 - hMSH6。