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MyoD介导的组织特异性基因激活:通过顺式作用抑制元件确定特异性

Tissue-specific gene activation by MyoD: determination of specificity by cis-acting repression elements.

作者信息

Weintraub H, Genetta T, Kadesch T

机构信息

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

出版信息

Genes Dev. 1994 Sep 15;8(18):2203-11. doi: 10.1101/gad.8.18.2203.

Abstract

MyoD is a muscle-specific transcriptional activator; E12 is a B-cell activator. An IgH enhancer is activated almost 100-fold by E12 but not at all by Myo; an MCK enhancer is activated almost 1000-fold by MyoD and not at all by E12. MyoD and E12 are both basic helix-loop-helix proteins that bind to similar E-box sequences (CANNTG); the IgH enhancer contains the same E boxes as the MCK enhancer, yet each retains exclusive specificity for either E12 or MyoD, respectively. We show that the IgH enhancer contains a cis-acting negative element that is directed at MyoD, but not at E12. This repression requires the mu E5 E box within the IgH enhancer; however, the specificity for repression, as opposed to activation, is associated with 2 bp flanking each side of the mu E5 E box. The target for repression of MyoD in the IgH enhancer is the bHLH region of MyoD. Our results suggest that MyoD only activates myogenic genes because nonmuscle enhancers that contain E boxes also contain negative elements that prevent MyoD activity.

摘要

肌分化蛋白(MyoD)是一种肌肉特异性转录激活因子;E12是一种B细胞激活因子。免疫球蛋白重链(IgH)增强子被E12激活近100倍,但完全不被MyoD激活;肌酸激酶(MCK)增强子被MyoD激活近1000倍,而完全不被E12激活。MyoD和E12都是碱性螺旋-环-螺旋蛋白,它们与相似的E盒序列(CANNTG)结合;IgH增强子与MCK增强子含有相同的E盒,但各自分别对E12或MyoD保持专一的特异性。我们发现IgH增强子含有一个针对MyoD的顺式作用负性元件,但不针对E12。这种抑制作用需要IgH增强子内的μE5 E盒;然而,与激活相反,抑制的特异性与μE5 E盒两侧各2个碱基对相关。IgH增强子中MyoD的抑制靶点是MyoD的碱性螺旋-环-螺旋区域。我们的结果表明,MyoD仅激活肌源性基因,因为含有E盒的非肌肉增强子也含有阻止MyoD活性的负性元件。

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