Bancroft J D, Schaefer L A, Degen S J
Division of Basic Science Research, Children's Hospital Research Foundation, Cincinnati, OH.
Gene. 1990 Nov 15;95(2):253-60. doi: 10.1016/0378-1119(90)90368-2.
The nt sequence of 6127 bp of sequence upstream of the human prothrombin-encoding gene (F2) has been determined. Since we previously characterized 417 bp of DNA immediately upstream from the transcription start point (tsp), 6544 bp of continuous flanking sequence are known. Eleven Alu repeat sequences present in this region comprise 45% of the sequence; other repetitive sequences were identified by searching GenBank. The tsp was found to be heterogeneous by exon mapping and primer extension analysis. To localize the cis-acting sequences responsible for the liver-specific expression of F2, hybrid cat genes were constructed with various lengths of F2 5'-flanking region cloned upstream from a promoterless cat gene. After transfection into HepG2 and HeLa cells, it was inferred that the region between nt -1101 and -798 was required for synthesis in HepG2 cells; no synthesis was observed using these constructs in HeLa cells. Two sequences for known liver-specific or regulatory cis-acting sequences were identified in this region.
已确定人凝血酶原编码基因(F2)上游6127 bp的核苷酸序列。由于我们之前已对转录起始点(tsp)上游紧邻的417 bp DNA进行了特征分析,因此已知有6544 bp的连续侧翼序列。该区域存在的11个Alu重复序列占序列的45%;通过搜索GenBank鉴定出了其他重复序列。通过外显子定位和引物延伸分析发现tsp是异质的。为了定位负责F2肝脏特异性表达的顺式作用序列,构建了杂种cat基因,其带有从无启动子的cat基因上游克隆的不同长度的F2 5'侧翼区域。转染到HepG2和HeLa细胞后,推断nt -1101至-798之间的区域是HepG2细胞合成所必需的;在HeLa细胞中使用这些构建体未观察到合成。在该区域鉴定出了两个已知的肝脏特异性或调节性顺式作用序列。