首页> 美国卫生研究院文献>Journal of Virology >The adenovirus E4 17-kilodalton protein complexes with the cellular transcription factor E2F altering its DNA-binding properties and stimulating E1A-independent accumulation of E2 mRNA.
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The adenovirus E4 17-kilodalton protein complexes with the cellular transcription factor E2F altering its DNA-binding properties and stimulating E1A-independent accumulation of E2 mRNA.

机译:腺病毒E4 17-千金蛋白与细胞转录因子E2F形成复合物从而改变其DNA结合特性并刺激E2 mRNA的E1A非依赖性积累。

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摘要

E2F is a cellular DNA-binding factor. Its binding activity is changed within adenovirus-infected cells so that it binds cooperatively to pairs of properly spaced and oriented E2F recognition sites. In the work described in this report, the conversion to cooperative binding was shown to require the adenovirus E4 17-kilodalton (kDa) polypeptide. Mutant viruses carrying alterations within the E4 17-kDa coding region failed to generate the infection-specific, cooperatively binding form of E2F. It was possible to alter E2F from uninfected cells so that it bound cooperatively by incubation with a partially purified fraction obtained from infected cells. The E4 17-kDa protein copurified with this activity and was also found to be present in a complex containing E2F. Consistent with its ability to alter the binding of E2F to its recognition sites within the E2 promoter, the E4 17-kDa polypeptide contributed to maximal expression of E2 mRNAs in some cell types. Its ability to enhance E2 transcription did not require expression of the E1A transactivator protein. These results are consistent with a model which proposes that the E4 17-kDa polypeptide binds to the cellular E2F factor, altering its binding behavior and thereby enhancing its ability to stimulate transcription.
机译:E2F是细胞DNA结合因子。它的结合活性在腺病毒感染的细胞内发生了变化,因此它与适当间隔且定向的E2F识别位点对协同结合。在本报告中描述的工作中,表明向协同结合的转化需要腺病毒E4 17-千达尔顿(kDa)多肽。在E4 17-kDa编码区内发生变异的突变病毒未能产生感染特异性的E2F协同结合形式。有可能改变未感染细胞的E2F,从而使其与从感染细胞获得的部分纯化级分一起温育,从而协同结合。 E4 17-kDa蛋白与该活性共纯化,并且还发现存在于含有E2F的复合物中。与它改变E2F与其在E2启动子内的识别位点的结合的能力一致,E4 17-kDa多肽有助于在某些细胞类型中E2 mRNA的最大表达。它增强E2转录的能力不需要表达E1A反式激活蛋白。这些结果与提出E4 17-kDa多肽结合细胞E2F因子,改变其结合行为并从而增强其刺激转录能力的模型相一致。

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