Quitschke W W, DePonti-Zilli L, Lin Z Y, Paterson B M
Laboratory of Biochemistry, National Cancer Institute, Bethesda, Maryland 20892.
Mol Cell Biol. 1989 Aug;9(8):3218-30. doi: 10.1128/mcb.9.8.3218-3230.1989.
The cis-acting regions that appear to be involved in negative regulation of the chicken alpha-cardiac actin promoter both in vivo and in vitro have been identified. A nuclear factor(s) binding to the proximal region mapped over the TATA element between nucleotides -50 and -25. In the distal region, binding spanned nucleotides -136 to -112, a region that included a second CArG box (CArG2) 5' to the more familiar CCAAT-box (CArG1) consensus sequence. Nuclear factors binding to these different domains were found in both muscle and nonmuscle preparations but were detectable at considerably lower levels in tissues expressing the alpha-cardiac actin gene. In contrast, concentrations of the beta-actin CCAAT-box binding activity were similar in all extracts tested. The role of these factor-binding domains on the activity of the cardiac actin promoter in vivo and in vitro and the prevalence of the binding factors in nonmuscle extracts are consistent with the idea that these binding domains and their associated factors are involved in the tissue-restricted expression of cardiac actin through both positive and negative regulatory mechanisms. In the absence of negative regulatory factors, these same binding domains act synergistically, via other factors, to activate the cardiac actin promoter during myogenesis.
已确定在体内和体外似乎参与鸡α-心肌肌动蛋白启动子负调控的顺式作用区域。一种核因子与定位在核苷酸-50至-25之间TATA元件上的近端区域结合。在远端区域,结合跨越核苷酸-136至-112,该区域在更常见的CCAAT框(CArG1)共有序列的5'端包含第二个CArG框(CArG2)。在肌肉和非肌肉制剂中均发现了与这些不同结构域结合的核因子,但在表达α-心肌肌动蛋白基因的组织中,其水平要低得多。相比之下,在所有测试提取物中,β-肌动蛋白CCAAT框结合活性的浓度相似。这些因子结合结构域在体内和体外对心肌肌动蛋白启动子活性的作用以及非肌肉提取物中结合因子的普遍性,与这些结合结构域及其相关因子通过正负调控机制参与心肌肌动蛋白的组织限制性表达的观点一致。在没有负调控因子的情况下,这些相同的结合结构域通过其他因子协同作用,在肌生成过程中激活心肌肌动蛋白启动子。