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Identification of transcriptional activation and inhibitory domains in serum response factor (SRF) by using GAL4-SRF constructs.

机译:通过使用GAL4-SRF构建体鉴定血清反应因子(SRF)中的转录激活和抑制域。

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摘要

The binding of serum response factor (SRF) to the c-fos serum response element has been shown to be essential for serum and growth factor activation of c-Fos. Since SRF is ubiquitously expressed, it has been difficult to measure the activity of SRF introduced into cells. To assay for functions of SRF in cells, we have changed its DNA binding specificity by fusing it to the DNA binding domain of GAL4. Transfection of GAL4-SRF constructs into cells has allowed us to identify SRF's transcriptional activation domain as well as domains which inhibit this activity. First, we found that the transcriptional activation domain maps to between amino acids 339 and 508 in HeLa cells and to between amino acids 414 and 508 in NIH 3T3 cells. Second, we show that in the context of GAL4-SRF constructs, there are two separate domains of SRF that can inhibit its activation domain. Although these domains overlap the DNA binding and dimerization domains of SRF, these functions were not required for inhibition. Finally, we show that one of the inhibitory domains is modular in that it can also inhibit activation when it is moved amino terminal to GAL4's DNA binding domain in an SRF-GAL4-SRF construct. The implications of these inhibitory domains for SRF regulation are discussed.
机译:血清反应因子(SRF)与c-fos血清反应元件的结合已显示对于c-Fos的血清和生长因子激活至关重要。由于SRF无处不在,因此很难测量引入细胞的SRF的活性。为了测定SRF在细胞中的功能,我们通过将其与GAL4的DNA结合域融合来改变其DNA结合特异性。 GAL4-SRF构建体转染到细胞中使我们能够鉴定SRF的转录激活结构域以及抑制该活性的结构域。首先,我们发现转录激活域映射到HeLa细胞中的339和508位氨基酸之间以及NIH 3T3细胞中的414和508位氨基酸之间。其次,我们表明在GAL4-SRF构建体的背景下,SRF有两个单独的域可以抑制其激活域。尽管这些结构域与SRF的DNA结合和二聚结构域重叠,但抑制这些功能并不是必需的。最后,我们表明抑制域之一是模块化的,因为当它在SRF-GAL4-SRF构建体中氨基末端移动到GAL4的DNA结合域时,它也可以抑制激活。讨论了这些抑制域对SRF调控的影响。

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