Yamaguchi Masayoshi, Murata Tomiyasu
Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA 30322, USA.
Laboratory of Analytical Neurobiology, Faculty of Pharmacy, Meijo University, Nagoya, Aichi 468-8503, Japan.
Biomed Rep. 2017 Apr;6(4):374-378. doi: 10.3892/br.2017.874. Epub 2017 Mar 17.
Regucalcin gene promoter region-related protein-p117 (RGPR-p117; gene symbol, ) was identified in 2001 as a novel transcription factor that specifically binds to a nuclear factor I consensus motif, TTGGC(N)CC in the promoter region of the regucalcin () gene. The human RGPR-p117 gene consists of 26 exons spanning ~4.1 kbp and is localized on chromosome 1q25.2. The nuclear translocation of cytoplasm RGPR-p117 is mediated via the protein kinase C-dependent signaling pathway. Overexpression of RGPR-p117 enhances the transcription activity of , and a protective effect on cell death by inhibition of gene expression levels of caspase-3, caspase-8 and FADD proteins that possess the TTGGC motif in the promoter region of those genes was revealed. RGPR-p117 has a crucial role as a transcription factor. Notably, RGPR-p117 was shown to localize in the plasma membranes, mitochondria and microsomes (endoplasmic reticulum; ER). RGPR-p117, which is located in the ER, was also shown to have a role as an ER export factor implicated in the transports of proteins and lipids. As a result of this finding, it was proposed in 2007 that RGPR-p117 is renamed SEC 16 homolog B, endoplasmic reticulum export factor (SEC16B). Recently, there is increasing evidence that RGPR-p117/SEC16B may be involved in human obesity. Thus, the current review presents data regarding the involvement of RGPR-p117 in human obesity.
调节钙素基因启动子区域相关蛋白-p117(RGPR-p117;基因符号, )于2001年被鉴定为一种新型转录因子,它能特异性结合调节钙素( )基因启动子区域的核因子I共有基序TTGGC(N)CC。人类RGPR-p117基因由26个外显子组成,跨度约4.1千碱基对,位于1号染色体的1q25.2位置。细胞质RGPR-p117的核转位是通过蛋白激酶C依赖性信号通路介导的。RGPR-p117的过表达增强了 的转录活性,并且通过抑制那些基因启动子区域具有TTGGC基序的半胱天冬酶-3、半胱天冬酶-8和FADD蛋白的基因表达水平,揭示了其对细胞死亡的保护作用。RGPR-p117作为转录因子具有关键作用。值得注意的是,RGPR-p117被证明定位于质膜、线粒体和微粒体(内质网;ER)。位于内质网中的RGPR-p117也被证明具有作为内质网输出因子参与蛋白质和脂质转运的作用。基于这一发现,2007年有人提议将RGPR-p117重新命名为内质网输出因子SEC 16同源物B(SEC16B)。最近,越来越多的证据表明RGPR-p117/SEC16B可能与人类肥胖有关。因此,本综述呈现了关于RGPR-p117参与人类肥胖的数据。