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不同的途径调节骨骼肌肌球蛋白重链基因的表达。

Different pathways regulate expression of the skeletal myosin heavy chain genes.

作者信息

Allen D L, Sartorius C A, Sycuro L K, Leinwand L A

机构信息

Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, Colorado 80309-0347, USA.

出版信息

J Biol Chem. 2001 Nov 23;276(47):43524-33. doi: 10.1074/jbc.M108017200. Epub 2001 Sep 10.

DOI:10.1074/jbc.M108017200
PMID:11551968
Abstract

Mammalian skeletal muscles are a mosaic of different fiber types largely defined by differential myosin heavy chain (MyHC) expression. Little is known about the molecular mechanisms regulating expression of the MyHC gene family members in different fiber types. In this work, we identified several cis- and trans-elements that regulate expression of the three adult fast MyHC genes. Despite multiple DNA-binding motifs for well characterized muscle transcription factors upstream of all three fast MyHC genes, expression of MyoD/Myf-5, calcineurin, or NFAT3 had different effects on the three promoters. MyoD or Myf-5 overexpression preferentially activated the IIb promoter, whereas NFAT or activated calcineurin overexpression preferentially activated the IIa promoter. Calcineurin had a 50-100-fold stimulatory effect on the IIa promoter, and the known downstream effectors of calcineurin (myocyte enhancer factor-2 and NFAT) cannot completely account for this activation. Finally, we identified two elements critical for regulating MyHC-IId/x expression: a 130-base pair enhancer element and a CArG-like element that inhibited IId/x promoter activity in vitro. Thus, we have found specific regulatory pathways that are distinct for the three adult fast MyHC genes. These elements are logical candidates for fiber-specific control of skeletal muscle gene expression in vivo.

摘要

哺乳动物的骨骼肌是由不同纤维类型组成的镶嵌体,主要由不同的肌球蛋白重链(MyHC)表达来定义。关于调节不同纤维类型中MyHC基因家族成员表达的分子机制,我们知之甚少。在这项研究中,我们鉴定了几个顺式和反式元件,它们调节三种成年快速MyHC基因的表达。尽管在所有三种快速MyHC基因上游存在多个特征明确的肌肉转录因子的DNA结合基序,但MyoD/Myf-5、钙调神经磷酸酶或NFAT3的表达对这三种启动子有不同的影响。MyoD或Myf-5的过表达优先激活IIb启动子,而NFAT或钙调神经磷酸酶的过表达优先激活IIa启动子。钙调神经磷酸酶对IIa启动子有50到100倍的刺激作用,而钙调神经磷酸酶已知的下游效应物(肌细胞增强因子-2和NFAT)不能完全解释这种激活。最后,我们鉴定了两个调节MyHC-IId/x表达的关键元件:一个130个碱基对的增强子元件和一个在体外抑制IId/x启动子活性的类CArG元件。因此,我们发现了三种成年快速MyHC基因特有的特定调节途径。这些元件是体内骨骼肌基因表达纤维特异性控制的合理候选者。

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