Park K Y, Roe J H
Department of Microbiology, College of Natural Sciences, Seoul National University, Korea.
Biochem Biophys Res Commun. 1996 Nov 21;228(3):745-51. doi: 10.1006/bbrc.1996.1726.
We have previously demonstrated the presence of three negative regulatory elements (NRE1, 2, and 3) in the upstream region of the bovine growth hormone (bGH) gene, whose sequences are similar to the binding elements of transcription factor YY1. The recombinant human YY1 protein indeed bound to these three NRE's in vitro, among which NRE1 is the strongest binding element. Both HeLa and rat pituitary GH3 nuclear extracts contained protein which caused the same retardation as YY1 binding in gel mobility shift assay. The specific band retarded by HeLa and GH3 nuclear extracts was competed out efficiently by a known YY1 binding element. Addition of antibodies against YY1 in the binding reaction produced a distinct supershifted band and/or caused reduction in the YY1-specific band. When the recombinant plasmids containing the chloramphenicol acetyltransferase (CAT) gene under the control of the bGH promoter were introduced together with the expression vector for YY1 into HeLa cells, the expression of the bGH promoter decreased with increasing amount of cotransfecting YY1 expression vector. These results demonstrate that YY1 or its very close homolog negatively regulates bGH expression via binding to NRE's.
我们先前已证明,在牛生长激素(bGH)基因上游区域存在三个负调控元件(NRE1、2和3),其序列与转录因子YY1的结合元件相似。重组人YY1蛋白确实在体外与这三个NRE结合,其中NRE1是最强的结合元件。在凝胶迁移率变动分析中,HeLa细胞和大鼠垂体GH3细胞核提取物均含有能产生与YY1结合相同阻滞效果的蛋白质。HeLa细胞和GH3细胞核提取物阻滞的特异性条带能被已知的YY1结合元件有效竞争。在结合反应中加入抗YY1抗体可产生明显的超迁移条带和/或导致YY1特异性条带减少。当将含有受bGH启动子控制的氯霉素乙酰转移酶(CAT)基因的重组质粒与YY1表达载体一起导入HeLa细胞时,随着共转染的YY1表达载体量增加,bGH启动子的表达下降。这些结果表明,YY1或其非常接近的同源物通过与NRE结合对bGH表达起负调控作用。