Giorgini Flaviano, Davies Holly G, Braun Robert E
Department of Genome Sciences, University of Washington, Seattle, WA, USA.
Development. 2002 Aug;129(15):3669-79. doi: 10.1242/dev.129.15.3669.
In developing male germ cells, newly synthesized protamine mRNAs are stored for up to 7 days before translational activation. Translational repression of protamine 1 (Prm1) mRNA requires sequences present in its 3' untranslated region (UTR) and substantial evidence suggests a role for the murine Y-box protein MSY4 in this process. To determine if MSY4 can mediate translational repression in vivo, we generated transgenic mice in which the temporal window of MSY4 expression was extended during spermatogenesis. Expression of MSY4 disrupted the normal completion of spermatogenesis and caused dominant sterility. Immunocytochemical analysis of several markers, including the protamines, indicated that MSY4 prevented normal activation of translation. mRNAs whose translation was inhibited contained at least one MSY4 RNA recognition site, suggesting sequence-dependent translational repression. Altered translational activation resulted in defective processing of protamine 2 and severe defects in sperm morphogenesis. These results suggest that MSY4 plays an active role in translational repression of several mRNAs in differentiating spermatids.
在发育中的雄性生殖细胞中,新合成的鱼精蛋白mRNA在翻译激活前可储存长达7天。鱼精蛋白1(Prm1)mRNA的翻译抑制需要其3'非翻译区(UTR)中存在的序列,大量证据表明小鼠Y盒蛋白MSY4在此过程中发挥作用。为了确定MSY4是否能在体内介导翻译抑制,我们构建了转基因小鼠,在精子发生过程中延长了MSY4的表达时间窗口。MSY4的表达破坏了精子发生的正常完成并导致显性不育。对包括鱼精蛋白在内的几种标志物的免疫细胞化学分析表明,MSY4阻止了正常的翻译激活。其翻译受到抑制的mRNA含有至少一个MSY4 RNA识别位点,提示序列依赖性翻译抑制。翻译激活的改变导致鱼精蛋白2加工缺陷和精子形态发生严重缺陷。这些结果表明,MSY4在分化精子细胞中几种mRNA的翻译抑制中发挥积极作用。