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Analysis of cis-regulatory elements in the 5' untranslated region of murine leukemia virus controlling protein expression

机译:鼠白血病病毒5'非翻译区控制蛋白表达的顺式调控元件分析

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摘要

It has previously been reported by us that high-level expression of the Env protein of Fr-MLV clone A8 in brains is crucial for induction of spongiform neurodegeneration, and that the 0.3-kb fragment containing the R, U5, and the 5' leader sequence of A8 is responsible for neuropathogenicity. In the present study, the role of the 5' untranslated region in protein expression was investigated. Luciferase expression vectors containing the LTR (R-U3-U5) and 5' leader sequence of A8 and non-neuropathogenic 57 Fr-MLV, designated gl-A8 and gl-57, and their chimeric vectors, were constructed, and transfected into rat glial cells F10. Replacement of the region containing the 3' half of R, U5, and 5' leader sequence of gl-A8 with that of 57 showed a reduction in luciferase activities, and replacement of this region of gl-57 with that of A8 showed increased luciferase activity. These results show that the region containing the 3' half of R, U5, and 5' leader sequence of A8 more efficiently up-regulates protein expression than 57. In particular, the 3' half of 5' leader of A8 was most responsible for the up-regulation of protein expression. Of interest, after replacement of the fragments between A8 and 57, changes in the activities of vectors containing A8-U3 paralleled the amount of mRNA, but the activities of vectors containing 57-U3 did not. Furthermore, it is suggested that the region containing R, U5, and the 5' leader sequence influences transcriptional or post-transcriptional steps, depending on the upstream sequence containing enhancer elements and promoter.
机译:先前我们曾报道过,Fr-MLV克隆A8的Env蛋白在脑中的高表达对于诱导海绵状神经变性至关重要,并且含有R,U5和5'前导序列的0.3kb片段A8的序列负责神经致病性。在本研究中,研究了5'非翻译区在蛋白质表达中的作用。构建了含有A8的LTR(R-U3-U5)和5'前导序列和非神经致病性57 Fr-MLV的萤光素酶表达载体,以及它们的嵌合载体,并将其转染到大鼠中胶质细胞F10。 gl-A8的R,U5和5'前导序列的3'一半区域替换为57的区域显示萤光素酶活性降低,而gl-57的该区域替换为A8的萤光素酶活性增加。活动。这些结果表明,包含A8的R,U5和5'前导序列的3'一半的区域比57更有效地上调蛋白质表达。特别是,A8的5'前导的3'一半是最主要的原因。蛋白质表达的上调。令人感兴趣的是,在替换A8和57之间的片段后,含有A8-U3的载体的活性变化与mRNA的量平行,但是含有57-U3的载体的活性却没有。此外,建议包含R,U5和5'前导序列的区域影响转录或转录后步骤,这取决于包含增强子元件和启动子的上游序列。

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