Teng Yen-Ni, Chuang Po-Jung, Liu Yo-Wen
Department of Biological Sciences and Technology, National University of Tainan, No.33, Sec. 2, Shulin St., West Central District, Tainan City 700, Taiwan.
Int J Mol Sci. 2012 Dec 28;14(1):625-39. doi: 10.3390/ijms14010625.
The human Leucine-rich Repeats and WD repeat Domain containing 1 (LRWD1) gene was originally identified by cDNA microarray as one of the genes down-regulated in the testicular tissues of patients with severe spermatogenic defects. Human LRWD1 is a testicular-enriched protein that is present predominantly in the cytoplasm of spermatocytes and spermatids and colocalizes with the centrosome at the base of sperm tail. Reporter assay, Chromatin immunoprecipitation (ChIP) analysis, and gel electrophoretic mobility shift assay (EMSA) were used to identify the core promoter region of LRWD1. A 198 bp segment upstream of the LRWD1 transcription initiation site exhibited promoter activity. The LRWD1 core promoter lacked a TATA box but contained a NF-κB binding site. Chromatin immunoprecipitation (ChIP) analysis and gel electrophoretic mobility shift assay (EMSA) showed basal binding of the NF-κB subunit to the LRWD1 promoter. LRWD1 promoter activity was positively regulated by NF-κB, and this regulation was dependent on the presence of the conserved κB site in the LRWD1 promoter region. Our data suggest that NF-κB is an important regulator for the expression of LRWD1. This is the first study showing that the expression of the testis-enriched LRWD1 gene is regulated by NF-κB.
人类富含亮氨酸重复序列和WD重复结构域蛋白1(LRWD1)基因最初是通过cDNA微阵列鉴定出来的,它是严重生精缺陷患者睾丸组织中下调的基因之一。人类LRWD1是一种睾丸富集蛋白,主要存在于精母细胞和精子细胞的细胞质中,并与精子尾部基部的中心体共定位。采用报告基因检测、染色质免疫沉淀(ChIP)分析和凝胶电泳迁移率变动分析(EMSA)来鉴定LRWD1的核心启动子区域。LRWD1转录起始位点上游198 bp的片段具有启动子活性。LRWD1核心启动子缺乏TATA盒,但含有一个NF-κB结合位点。染色质免疫沉淀(ChIP)分析和凝胶电泳迁移率变动分析(EMSA)显示NF-κB亚基与LRWD1启动子存在基础结合。LRWD1启动子活性受NF-κB正向调控,且这种调控依赖于LRWD1启动子区域中保守的κB位点的存在。我们的数据表明NF-κB是LRWD1表达的重要调节因子。这是第一项表明睾丸富集的LRWD1基因表达受NF-κB调控的研究。