无内含子mRNA表达的两种不同途径:一种与人类免疫缺陷病毒Rev和人类T细胞白血病病毒I型Rex功能相关,另一种无关。

T Kiyokawa, T Umemoto, Y Watanabe, S Matsushita, H Shida
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引用次数: 9

摘要

根据其表达对TAgRex(人类T细胞白血病病毒I型Rex蛋白的显性阴性突变体)抑制作用的敏感性,以及它们表达人类免疫缺陷病毒(HIV)基因组内含子编码基因的能力,将无内含子mrna分为两类。干扰素- α mRNA不能诱导HIV病毒env基因的表达,其表达对TAgRex具有抗性。相比之下,乙肝病毒核胞质输出mrna所必需的转录后调控元件(PRE)诱导了位于HIV基因组内含子内的氯霉素乙酰转移酶基因的表达。TAgRex抑制预介导表达。因此,这些结果表明,至少存在两种不同的无内含子mRNA表达途径,一种与Rev和Rex功能相关,另一种与Rev和Rex功能无关。
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Two distinct pathways for intronless mRNA expression: one related, the other unrelated to human immunodeficiency virus Rev and human T cell leukemia virus type I Rex functions.

Intronless mRNAs were classified into two classes based on the sensitivities of their expression to the inhibitory effect of TAgRex, a dominant-negative mutant of the Rex protein of human T cell leukemia virus type I, and their abilities to express the genes encoded in the intron of the human immunodeficiency virus (HIV) genome. Interferon-alpha mRNA could not induce the expression of the env gene of HIV, and its expression was resistant to TAgRex. In contrast, the posttranscriptional regulatory element (PRE), necessary for the nucleo-cytoplasmic export of mRNAs of hepatitis B virus, induced expression of the chloramphenicol acetyl transferase gene located within the intron of the HIV genome. PRE-mediated expression was inhibited by TAgRex. Thus, these results suggest that there are at least two distinct pathways for intronless mRNA expression, one related to and the other unrelated to Rev and Rex functions.

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