Zeng Mei, Sun Huaqin, Chen Shu, Wang Xinying, Yang Yuan, Liu Yunqiang, Tao Dachang, Yang Zhirong, Zhang Sizhong, Ma Yongxin
Department of Medical Genetics, West China Hospital, Sichuan University, Renmin Nanlu, Section 3 #17, Chengdu 610041, PR China.
Mol Hum Reprod. 2008 Jun;14(6):331-6. doi: 10.1093/molehr/gan024. Epub 2008 May 20.
Rbmy gene encodes a RNA-binding protein and its expression is limited to the nuclei of germ cells. Previous studies indicate that RBMY may function in pre-mRNA processing during spermatogenesis, although its precise target mRNAs remain unclear. By using specific nucleic acids associated with proteins and immunoprecipitation techniques, we have identified 12 potential target mRNAs bound by mouse RBMY protein from testis. We detect that both mRbmy-1 and mRbmy-2 transcripts co-exist in mouse testis and they differ mainly in the 5'UTR. Importantly, our result shows that mRBMY protein can bind to one of its own transcripts, mRbmy-2, suggesting that mRBMY may affect alternative splicing or regulate the expression of its own gene. Using electrophoretic mobility shift assay, we demonstrated that mRBMY protein can bind to the testis and sperm-specific spa17 mRNA and that the binding domain contains rich oligo(A), suggesting that mRBMY protein may have high affinity to oligo(A) rich sequences. In conclusion, the identification of RBMY target mRNAs will be helpful to further explore the biological function of RBMY in spermatogenesis.
Rbmy基因编码一种RNA结合蛋白,其表达仅限于生殖细胞的细胞核。先前的研究表明,RBMY可能在精子发生过程中的前体mRNA加工中发挥作用,尽管其确切的靶mRNA仍不清楚。通过使用与蛋白质相关的特异性核酸和免疫沉淀技术,我们从睾丸中鉴定出了12种与小鼠RBMY蛋白结合的潜在靶mRNA。我们检测到mRbmy-1和mRbmy-2转录本在小鼠睾丸中共同存在,它们主要在5'UTR区域存在差异。重要的是,我们的结果表明mRBMY蛋白可以结合其自身的一种转录本mRbmy-2,这表明mRBMY可能影响可变剪接或调节其自身基因的表达。使用电泳迁移率变动分析,我们证明mRBMY蛋白可以结合睾丸和精子特异性的spa17 mRNA,并且结合结构域包含丰富的寡聚(A),这表明mRBMY蛋白可能对富含寡聚(A)的序列具有高亲和力。总之,RBMY靶mRNA的鉴定将有助于进一步探索RBMY在精子发生中的生物学功能。