Tafuri S R, Familari M, Wolffe A P
Laboratory of Molecular Embryology, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.
J Biol Chem. 1993 Jun 5;268(16):12213-20.
We have isolated a mouse cDNA clone, which encodes the protein MSY1 (mouse Y box protein 1), a new member of the Y box family of proteins. Northern analysis indicates that MSY1 mRNA accumulates over 100-fold more in testis than in other tissues. Moreover, MSY1 mRNA is developmentally regulated, initially appearing at the pachytene stage of spermatogenesis. This is the stage of maximal transcription and translation in the spermatocyte. In Xenopus laevis, homologous Y box proteins, FRGY1 and FRGY2, positively regulate transcription from promoters containing a Y box (CTGATTGGCCAA). In addition, the germ cell-specific Y box protein FRGY2 binds maternal mRNA within 60-80 S mRNP storage particles and in doing so regulates translation in the developing oocyte and embryo (Smith, L. D., Richter, J. D., and Taylor, M. A. (1984) in Molecular Biology of Development (Davidson, E. R., and Firtel, R. A., eds) pp. 129-141, Alan R. Liss, New York). The MSY1 protein can be isolated from a 60-80 S mRNP fraction of testis which like the frog oocyte contains stored, untranslated mRNAs. Furthermore, cross-linking experiments demonstrate that MSY1 is bound to mRNAs of this fraction. Finally, mobility shift analysis performed using the isolated protein indicates that MSY1 has nucleic acid binding properties similar to those of the FRGY proteins. These data suggest that the mouse Y box protein, MSY1, functions similarly to the FRGY2 protein in regulating the storage and translation of germ cell RNAs.
我们分离出了一个小鼠cDNA克隆,它编码蛋白质MSY1(小鼠Y盒蛋白1),这是Y盒蛋白家族的一个新成员。Northern分析表明,MSY1 mRNA在睾丸中的积累量比在其他组织中多100倍以上。此外,MSY1 mRNA受到发育调控,最初出现在精子发生的粗线期。这是精母细胞中转录和翻译最为活跃的阶段。在非洲爪蟾中,同源Y盒蛋白FRGY1和FRGY2对含有Y盒(CTGATTGGCCAA)的启动子的转录起正向调节作用。此外,生殖细胞特异性Y盒蛋白FRGY2与60 - 80 S mRNP储存颗粒中的母体mRNA结合,从而在发育中的卵母细胞和胚胎中调节翻译(史密斯,L.D.,里希特,J.D.,和泰勒,M.A.(1984年),载于《发育分子生物学》(戴维森,E.R.,和菲尔特尔,R.A.编),第129 - 141页,阿兰·R·利斯出版社,纽约)。MSY1蛋白可以从睾丸的60 - 80 S mRNP组分中分离出来,该组分与蛙卵母细胞一样含有储存的未翻译mRNA。此外,交联实验表明MSY1与该组分的mRNA结合在一起。最后,使用分离出的蛋白进行的迁移率变动分析表明,MSY1具有与FRGY蛋白相似的核酸结合特性。这些数据表明,小鼠Y盒蛋白MSY1在调节生殖细胞RNA的储存和翻译方面,其功能与FRGY2蛋白相似。