Yang Juxiang, Medvedev Sergey, Yu Junying, Tang Linda C, Agno Julio E, Matzuk Martin M, Schultz Richard M, Hecht Norman B
Center for Research on Reproduction and Women's Health and Department of Biology, University of Pennsylvania School of Medicine, 421 Curie Boulevard, Philadelphia, PA 19104, USA.
Proc Natl Acad Sci U S A. 2005 Apr 19;102(16):5755-60. doi: 10.1073/pnas.0408718102. Epub 2005 Apr 11.
MSY2, a germ-cell-specific member of the Y-box family of DNA-/RNA-binding proteins, is proposed to function as a coactivator of transcription in the nucleus and to stabilize and store maternal and paternal mRNAs in the cytoplasm. In mice lacking Msy2, a normal Mendelian ratio is observed after matings between heterozygotes with equal numbers of phenotypically normal but sterile male and female homozygotes (Msy2-/-). Spermatogenesis is disrupted in postmeiotic null germ cells with many misshapen and multinucleated spermatids, and no spermatozoa are detected in the epididymis. Apoptosis is increased in the testes of homozygotes, and real-time RT-PCR assays reveal large reductions in the mRNA levels of postmeiotic male germ cell mRNAs and smaller reductions of meiotic germ cell transcripts. In females, there is no apparent decrease in either the number of follicles or their morphology in ovaries obtained from 2- and 8-day-old Msy2-/- mice. In contrast, follicle number and progression are reduced in 21-day-old Msy2-/- ovaries. In adult Msy2-/- females, oocyte loss increases, anovulation is observed, and multiple oocyte and follicle defects are seen. Thus, Msy2 represents one of a small number of germ-cell-specific genes whose deletion leads to the disruption of both spermatogenesis and oogenesis.
MSY2是DNA/RNA结合蛋白Y盒家族中一种生殖细胞特异性成员,被认为在细胞核中作为转录共激活因子发挥作用,并在细胞质中稳定和储存母源和父源mRNA。在Msy2基因敲除的小鼠中,杂合子之间交配后,观察到孟德尔比率正常,产生数量相等的表型正常但不育的雄性和雌性纯合子(Msy2-/-)。减数分裂后缺失Msy2的生殖细胞中精子发生受到破坏,出现许多畸形和多核精子细胞,附睾中未检测到精子。纯合子睾丸中的细胞凋亡增加,实时RT-PCR分析显示减数分裂后雄性生殖细胞mRNA水平大幅降低,减数分裂生殖细胞转录本水平降低幅度较小。在雌性中,从2日龄和8日龄Msy2-/-小鼠获得的卵巢中,卵泡数量及其形态均无明显减少。相比之下,21日龄Msy2-/-卵巢中的卵泡数量和发育进程减少。在成年Msy2-/-雌性小鼠中,卵母细胞损失增加,观察到无排卵现象,并且出现多个卵母细胞和卵泡缺陷。因此,Msy2是少数几种生殖细胞特异性基因之一,其缺失会导致精子发生和卵子发生均受到破坏。