Zhou Jianlin, Fan Changzheng, Zhong Yingli, Liu Yunhai, Liu Mingjun, Zhou Aidong, Ren Kaiqun, Zhang Jian
Department of Biochemistry and Molecular Biology, College of Life Science, Hunan Normal University, Changsha, Hunan 410081, China.
FEBS Lett. 2005 Mar 14;579(7):1715-22. doi: 10.1016/j.febslet.2005.02.027.
The mouse polymerase delta-interacting protein 1 gene, PDIP1, is mapped to chromosome 7F3 region, spans approximately 16.7kb, and is organized into six exons. The transcription start site (TSS) was determined to be G, corresponding to position of 162-bp upstream of the translation start codon. The promoter region was found to lack TATA box or CCAAT box, instead, a CpG island was detected surrounding TSS. The region from -162 to +114 is required for basal transcriptional regulation of mouse PDIP1 gene, contains two AP-2 and two Sp1 binding sites. The Sp1 site upstream of TSS activates, while the other Sp1 site and two AP-2 sites suppress the transcription activity of mouse PDIP1 gene.
小鼠聚合酶δ相互作用蛋白1基因(PDIP1)定位于7F3染色体区域,跨度约16.7kb,由六个外显子组成。转录起始位点(TSS)确定为G,对应于翻译起始密码子上游162bp的位置。发现启动子区域缺乏TATA盒或CCAAT盒,相反,在TSS周围检测到一个CpG岛。从-162到+114的区域是小鼠PDIP1基因基础转录调控所必需的,包含两个AP-2和两个Sp1结合位点。TSS上游的Sp1位点激活,而其他Sp1位点和两个AP-2位点抑制小鼠PDIP1基因的转录活性。