Bengal E, Flores O, Rangarajan P N, Chen A, Weintraub H, Verma I M
Salk Institute, San Diego, CA 92186-5800.
Proc Natl Acad Sci U S A. 1994 Jun 21;91(13):6221-5. doi: 10.1073/pnas.91.13.6221.
An in vitro transcription system from HeLa cells has been established in which MyoD and E47 proteins activate transcription both as homodimers and heterodimers. However, heterodimers activate transcription more efficiently than homodimers, and function synergistically from multiple binding sites. Positive control mutants in the basic region of MyoD that have previously been shown to be defective in initiating the myogenic program, can bind DNA but have lost their ability to function as transcriptional activators in vitro. Additionally, positive control mutants, unlike wild-type MyoD, fail to bind cooperatively to DNA. We propose that binding of MyoD complexes to high affinity MyoD binding sites induces conformational changes that facilitate cooperative binding to multiple sites and promote transcriptional activation.
已建立一种来自HeLa细胞的体外转录系统,其中MyoD和E47蛋白作为同二聚体和异二聚体均可激活转录。然而,异二聚体比同二聚体更有效地激活转录,并且从多个结合位点协同发挥作用。MyoD碱性区域的阳性对照突变体先前已被证明在启动肌生成程序方面存在缺陷,它们能够结合DNA,但在体外已丧失作为转录激活因子发挥作用的能力。此外,与野生型MyoD不同,阳性对照突变体不能与DNA协同结合。我们提出,MyoD复合物与高亲和力MyoD结合位点的结合会诱导构象变化,从而促进与多个位点的协同结合并促进转录激活。