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鸡心脏和肝脏中肌钙蛋白C基因的缓慢表达受相似增强子调控。

Slow troponin C gene expression in chicken heart and liver is regulated by similar enhancers.

作者信息

Grewal J S, Bag J

机构信息

Department of Molecular Biology and Genetics, University of Guelph, Ont., Canada.

出版信息

FEBS Lett. 1996 Apr 1;383(3):267-72. doi: 10.1016/0014-5793(96)00247-5.

Abstract

Two isoforms of troponin C (TnC) are encoded by distinct single copy genes. Expression of fast TnC is restricted to the skeletal muscle, whereas the slow isoform is expressed in both skeletal and cardiac muscle. Chicken slow TnC (cTnC) gene is also expressed in some non-muscle tissues like the liver and the brain. Expression of cTnC gene is regulated by two distinct enhancers in cardiac and skeletal muscles. The cardiac specific enhancer is located in the immediate 5' flanking region (bp-124 to -79) of the murine cTnC gene whereas the skeletal enhancer is located within the first intron (bp 997 to 1141). In the present study we have examined how cTnC gene expression is regulated in the chicken liver. Transient transfection of liver cells with CTnC-CAT reporter constructs containing various regions of the murine cTnC gene showed that its expression in chicken liver is regulated by the cardiac specific enhancer. Furthermore, electrophoretic mobility shift assays using synthetic oligonucleotides corresponding to both CEF-1 and CEF-2 regions of the murine cardiac enhancer revealed formation of specific DNA-protein complexes. Ultraviolet light induced covalent linking of nuclear proteins to CEF-1 and CEF-2 oligomers were used to examine the nature of the cardiac enhancer binding polypeptides; one polypeptide of 48 kDa appeared to bind to both CEF-1 and CEF-2 sequences.

摘要

肌钙蛋白C(TnC)的两种同工型由不同的单拷贝基因编码。快速TnC的表达仅限于骨骼肌,而慢速同工型在骨骼肌和心肌中均有表达。鸡的慢速TnC(cTnC)基因在肝脏和大脑等一些非肌肉组织中也有表达。cTnC基因的表达受心肌和骨骼肌中两个不同增强子的调控。心肌特异性增强子位于小鼠cTnC基因紧邻的5'侧翼区域(碱基对-124至-79),而骨骼肌增强子位于第一个内含子内(碱基对997至1141)。在本研究中,我们研究了鸡肝脏中cTnC基因表达是如何调控的。用含有小鼠cTnC基因各个区域的CTnC-CAT报告基因构建体对肝细胞进行瞬时转染,结果表明其在鸡肝脏中的表达受心肌特异性增强子的调控。此外,使用与小鼠心肌增强子的CEF-1和CEF-2区域相对应的合成寡核苷酸进行电泳迁移率变动分析,揭示了特异性DNA-蛋白质复合物的形成。利用紫外线诱导核蛋白与CEF-1和CEF-2寡聚体的共价连接来检测心肌增强子结合多肽的性质;一种48 kDa的多肽似乎与CEF-1和CEF-2序列都结合。

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