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MyoD对肌肉特异性的转录激活作用。

Muscle-specific transcriptional activation by MyoD.

作者信息

Weintraub H, Dwarki V J, Verma I, Davis R, Hollenberg S, Snider L, Lassar A, Tapscott S J

机构信息

Fred Hutchinson Cancer Research Center, Howard Hughes Medical Institute Laboratory, Seattle, Washington 98104.

出版信息

Genes Dev. 1991 Aug;5(8):1377-86. doi: 10.1101/gad.5.8.1377.

Abstract

We focus on the mechanism by which MyoD activates transcription. Previous experiments showed that when the 13-amino-acid basic region of E12 replaced the corresponding basic region of MyoD, the resulting MyoD-E12Basic chimeric protein could bind specifically to muscle-specific enhancers in vitro and form dimers with E12, but could not activate a cotransfected reporter gene or convert 10T1/2 cells to muscle. Here we show that back mutation of this chimeric protein (with the corresponding residues in MyoD) re-establishes activation, and we identify a specific alanine involved in increasing DNA binding and a specific threonine required for activation. Using a reporter gene containing MyoD-binding sites located downstream from the transcription start site, we show that MyoD-E12Basic can bind in vivo and thereby inhibit expression of the reporter. In vivo binding is also supported by the fact that the addition of the "constitutive" VP16 activation domain to MyoD-E12Basic restores full trans-activation potential. The normal MyoD-activation domain maps within the amino-terminal 53 residues and can be functionally replaced by the activation domain of VP16. The activity of the MyoD-activation domain is dramatically elevated when deletions are made almost anywhere in the rest of the MyoD molecule, suggesting that the activation domain in MyoD is usually masked. Surprisingly, MyoD-E12Basic can activate transcription in CV1 and B78 cells (but not in 10T1/2 or 3T3 cells), suggesting that the activation function of the basic domain requires a specific factor present in CV1 and B78 cells. We propose that to function, the masked MyoD-activation domain requires the participation of a second factor that recognizes the basic region. We refer to such a factor as a recognition factor.

摘要

我们专注于肌分化因子(MyoD)激活转录的机制。先前的实验表明,当E12的13个氨基酸的碱性区域取代MyoD的相应碱性区域时,所产生的MyoD-E12碱性嵌合蛋白在体外能够特异性结合肌肉特异性增强子并与E12形成二聚体,但无法激活共转染的报告基因,也不能将10T1/2细胞转化为肌肉细胞。在此我们表明,该嵌合蛋白的回突变(用MyoD中的相应残基)可重新建立激活作用,并且我们鉴定出一个参与增强DNA结合的特定丙氨酸和激活所需的一个特定苏氨酸。使用一个包含位于转录起始位点下游的MyoD结合位点的报告基因,我们表明MyoD-E12碱性蛋白能够在体内结合,从而抑制报告基因的表达。MyoD-E12碱性蛋白添加“组成型”病毒蛋白16(VP16)激活结构域可恢复完全的反式激活潜能,这一事实也支持了体内结合的观点。正常的MyoD激活结构域定位于氨基末端的53个残基内,并且可以被VP16的激活结构域功能性取代。当在MyoD分子其余部分的几乎任何位置进行缺失时,MyoD激活结构域的活性会显著提高,这表明MyoD中的激活结构域通常被掩盖。令人惊讶的是,MyoD-E12碱性蛋白能够在CV1和B78细胞中激活转录(但在10T1/2或3T3细胞中不能),这表明碱性结构域的激活功能需要CV1和B78细胞中存在的一种特定因子。我们提出,为发挥功能,被掩盖的MyoD激活结构域需要第二种识别碱性区域的因子的参与。我们将这样一种因子称为识别因子。

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