首页> 美国卫生研究院文献>Journal of Virology >Various modes of basic helix-loop-helix protein-mediated regulation of murine leukemia virus transcription in lymphoid cell lines.
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Various modes of basic helix-loop-helix protein-mediated regulation of murine leukemia virus transcription in lymphoid cell lines.

机译:基本的螺旋-环-螺旋蛋白介导的淋巴样细胞系小鼠白血病病毒转录调控的各种模式。

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摘要

The transcriptionally regulatory regions of the lymphomagenic Akv and SL3-3 murine leukemia retroviruses (MLVs) contain two types of E-box consensus motifs, CAGATG. One type, EA/S, is located in the upstream promoter region, and the other, E(gre), is located in a tandem repeat with enhancer properties. We have examined the requirements of the individual E-boxes in MLV transcriptional regulation. In lymphoid cell lines only, the E(gre)-binding protein complexes included ALF1 or HEB and E2A basic helix-loop-helix proteins. Ectopic ALF1 and E2A proteins required intact E(gre) motifs for mediating transcriptional activation. ALF1 transactivated transcription of Akv MLV through the two E(gre) motifs equally, whereas E2A protein required the promoter-proximal E(gre) motif. In T- and B-cell lines, the E(gre) motifs were of major importance for Akv MLV transcriptional activity, while the EA/S motif had some effect. In contrast, neither E(gre) nor EA/S motifs contributed pronouncedly to Akv MLV transcription in NIH 3T3 cells lacking DNA-binding ALF1 or HEB and E2A proteins. The Id1 protein was found to repress ALF1 activity in vitro and in vivo. Moreover, ectopic Id1 repressed E(gre)-directed but not EA/S-directed MLV transcription in lymphoid cell lines. In conclusion, E(gre) motifs and interacting basic helix-loop-helix proteins are important determinants for MLV transcriptional activity in lymphocytic cell lines.
机译:产生淋巴瘤的Akv和SL3-3鼠类白血病逆转录病毒(MLV)的转录调控区包含两种类型的E-box共有基序,即CAGATG。一种类型的EA / S位于上游启动子区域,另一种类型的E(gre)位于具有增强子特性的串联重复序列中。我们已经检查了MLV转录调控中各个E-box的要求。仅在淋巴样细胞系中,E(gre)结合蛋白复合物包括ALF1或HEB和E2A基本螺旋-环-螺旋蛋白。异位ALF1和E2A蛋白需要完整的E(gre)主题来介导转录激活。 ALF1通过两个E(gre)基序平等地激活Akv MLV的转录,而E2A蛋白则需要启动子附近的E(gre)基序。在T细胞和B细胞系中,E(gre)基序对于Akv MLV转录活性至关重要,而EA / S基序具有一定作用。相比之下,E(gre)和EA / S模体均对缺乏DNA结合ALF1或HEB和E2A蛋白的NIH 3T3细胞的Akv MLV转录没有明显贡献。发现Id1蛋白在体外和体内均抑制ALF1活性。此外,异位Id1抑制淋巴样细胞系中E(gre)指导但不是EA / S指导的MLV转录。总之,E(gre)主题和相互作用的基本螺旋-环-螺旋蛋白是淋巴细胞中MLV转录活性的重要决定因素。

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