Chang Guobin, Chen Rong, Xu Lu, Ma Teng, Wang Hongzhi, Chen Jing, Zhang Yang, Li Zhiteng, Wan Fang, Guo Xiaomin, Xu Qi, Zhao Wenming, Chen Guohong
College of Animal Science and Technology, Yangzhou University, Yangzhou 225009, China.
College of Animal Science and Technology, Yangzhou University, Yangzhou 225009, China; Institute of Animal Science, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China.
Anim Reprod Sci. 2015 Nov;162:95-103. doi: 10.1016/j.anireprosci.2015.09.016. Epub 2015 Sep 30.
The P-element induced wimpy testis (Piwi) protein family, a subfamily of the Argonaute protein family, is involved in gene silencing and shows specific expression in spermatogenic cells. To reveal the transcriptional regulatory mechanisms of Piwil1 in chickens, we cloned sequences of the chicken Piwil1 promoter region and performed luciferase reporter and electrophoretic mobility shift assays to analyze the transcriptional activity and identify important transcriptional regulatory elements. The results showed that the region from -90 to -43 in the 5'-flanking region of Piwil1 contains a transcriptional regulatory CCAAT box that was necessary for the transcriptional activity of the Piwil1 promoter. Moreover, the transcription factor nuclear factor Y (NF-Y) was bound to the Piwil1 promoter CCAAT box specifically in germ cells. In addition, bisulfite sequencing to determine the methylation profile of the Piwil1 promoter CpG island in different spermatogenic and non-germ cell populations was performed. Compared with germ cells, non-germ cells showed increased methylation of the promoter region containing the CCAAT box, loss of NF-Y binding, and silencing of the Piwil1 locus. It is demonstrated that the specific expression of Piwil1 in chicken germ cells is regulated by the transcription factor NF-Y and differential CpG island methylation.
P 元件诱导的弱精睾丸(Piwi)蛋白家族是 Argonaute 蛋白家族的一个亚家族,参与基因沉默,并在生精细胞中特异性表达。为了揭示鸡 Piwil1 的转录调控机制,我们克隆了鸡 Piwil1 启动子区域的序列,并进行了荧光素酶报告基因和电泳迁移率变动分析,以分析转录活性并鉴定重要的转录调控元件。结果表明,Piwil1 的 5'侧翼区域中从 -90 到 -43 的区域包含一个转录调控 CCAAT 框,这是 Piwil1 启动子转录活性所必需的。此外,转录因子核因子 Y(NF-Y)在生殖细胞中特异性地与 Piwil1 启动子 CCAAT 框结合。另外,进行了亚硫酸氢盐测序以确定不同生精细胞和非生殖细胞群体中 Piwil1 启动子 CpG 岛的甲基化谱。与生殖细胞相比,非生殖细胞中含有 CCAAT 框的启动子区域甲基化增加,NF-Y 结合丧失,Piwil1 基因座沉默。结果表明,鸡生殖细胞中 Piwil1 的特异性表达受转录因子 NF-Y 和差异 CpG 岛甲基化的调控。