Iguchi-Ariga S M, Okazaki T, Itani T, Ogata M, Sato Y, Ariga H
Institute of Medical Science, University of Tokyo, Japan.
EMBO J. 1988 Oct;7(10):3135-42. doi: 10.1002/j.1460-2075.1988.tb03180.x.
We have previously reported that c-myc protein may promote cellular DNA replication by binding to initiation sites of replication. Here we report that a putative origin of human cellular DNA replication (ori) is present at approximately 2 kb upstream of the coding region of the c-myc gene itself. The c-myc protein, or protein(s) complexed with c-myc protein, bind to the upstream region (approximately 200 bp in length) which has transcriptional enhancer activity as well as autonomously replicating activity in human cells, suggesting that the c-myc protein may be an enhancer binding protein as well as a DNA replication protein. Results with deletion mutants suggest that the sequence essential to the origin of DNA replication may be adjacent to, but cannot be clearly separated from, the sequence responsible for enhancer activity. Furthermore, when cloned DNA containing putative c-myc protein binding sequences was transfected as competitor into HL-60 cells, expression of c-myc was inhibited, suggesting that c-myc protein itself may be necessary for c-myc expression.
我们之前报道过,c-myc蛋白可能通过与复制起始位点结合来促进细胞DNA复制。在此我们报道,人类细胞DNA复制的一个假定起始点(ori)位于c-myc基因自身编码区上游约2 kb处。c-myc蛋白或与c-myc蛋白复合的蛋白结合到上游区域(长度约200 bp),该区域在人类细胞中具有转录增强子活性以及自主复制活性,这表明c-myc蛋白可能既是一种增强子结合蛋白,也是一种DNA复制蛋白。缺失突变体的结果表明,DNA复制起始点所必需的序列可能与负责增强子活性的序列相邻,但无法明确分离。此外,当将含有假定的c-myc蛋白结合序列的克隆DNA作为竞争者转染到HL-60细胞中时,c-myc的表达受到抑制,这表明c-myc蛋白本身可能是c-myc表达所必需的。