Yu Zuoren, Raabe Tobias, Hecht Norman B
Center for Research on Reproduction and Women's Health, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.
Biol Reprod. 2005 Sep;73(3):427-33. doi: 10.1095/biolreprod.105.040998. Epub 2005 May 18.
MicroRNAs play important roles in regulating development at both transcriptional and posttranscriptional levels. Here, we report 29 microRNAs from mouse testis that are differentially expressed as the prepubertal testis differentiates to the adult testis. Using computational analyses to identify potential microRNA target mRNAs, we identify several possible male germ cell target mRNAs. One highly conserved sequence in the 3'-untranslated region (UTR) of transition protein 2 (Tnp2) mRNA, a testis-specific and posttranscriptionally regulated mRNA in postmeiotic germ cells, is complementary to Mirn122a. Mirn122a is enriched in late-stage male germ cells and is predominantly on polysomes. Mirn122a, but not another noncomplementary microRNA, inhibits the activity of a luciferase reporter construct containing the 3'-UTR of Tnp2. Site-directed mutations of Mirn122a indicate that base pairing of the 5'-region of Mirn122a to its complementary site in the 3'-UTR of Tnp2 mRNA is essential for the downregulation of luciferase activity. Real-time reverse transcription-polymerase chain reaction and ribonuclease protection assays reveal that the Mirn122a-directed decrease of the Tnp2 reporter gene activity results from mRNA cleavage. We propose that specific microRNAs, such as Mirn122a, could be involved in the posttranscriptional regulation of mRNAs such as Tnp2 in the mammalian testis.
微小RNA在转录和转录后水平的发育调控中发挥着重要作用。在此,我们报告了来自小鼠睾丸的29种微小RNA,它们在青春期前睾丸向成年睾丸分化过程中差异表达。通过计算分析来鉴定潜在的微小RNA靶标mRNA,我们确定了几种可能的雄性生殖细胞靶标mRNA。过渡蛋白2(Tnp2)mRNA的3'-非翻译区(UTR)中有一个高度保守的序列,Tnp2是减数分裂后生殖细胞中睾丸特异性且受转录后调控的mRNA,该序列与Mirn122a互补。Mirn122a在晚期雄性生殖细胞中富集,且主要存在于多核糖体上。Mirn122a而非另一种非互补微小RNA抑制了包含Tnp2 3'-UTR的荧光素酶报告构建体的活性。对Mirn122a进行定点突变表明,Mirn122a 5'-区域与Tnp2 mRNA 3'-UTR中其互补位点的碱基配对对于荧光素酶活性的下调至关重要。实时逆转录-聚合酶链反应和核糖核酸酶保护分析表明,Mirn122a介导的Tnp2报告基因活性降低是由mRNA切割导致的。我们提出,特定的微小RNA,如Mirn122a,可能参与哺乳动物睾丸中Tnp2等mRNA的转录后调控。