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HIV-1长末端重复序列包含一个异常元件,该元件可诱导从各种mRNA和snRNA启动子合成短RNA。

The HIV-1 long terminal repeat contains an unusual element that induces the synthesis of short RNAs from various mRNA and snRNA promoters.

作者信息

Ratnasabapathy R, Sheldon M, Johal L, Hernandez N

机构信息

Cold Spring Harbor Laboratory, New York 11724.

出版信息

Genes Dev. 1990 Dec;4(12A):2061-74. doi: 10.1101/gad.4.12a.2061.

DOI:10.1101/gad.4.12a.2061
PMID:2269426
Abstract

We describe an unusual element that activates the synthesis of short transcripts from a wide variety of mRNA and small nuclear RNA (snRNA) promoters, including the U6 RNA polymerase III promoter. This inducer of short transcripts (IST) is located between positions -5 and +82 relative to the cap site in the HIV-1 LTR. In the presence of IST, the total transcriptional activity of the different promoters is greatly increased, but the resulting additional RNA molecules are short, ending around position +60. IST is not the RNA target (TAR) for Tat trans-activation; however, because it relies entirely on cellular factors for activity, IST may serve to provide abundant RNA targets for Tat trans-activation without a requirement for full-length viral mRNA expression.

摘要

我们描述了一种不寻常的元件,它可激活多种信使核糖核酸(mRNA)和小核核糖核酸(snRNA)启动子(包括U6 RNA聚合酶III启动子)的短转录本合成。这种短转录本诱导剂(IST)位于相对于HIV-1长末端重复序列(LTR)中帽位点的-5至+82位之间。在IST存在的情况下,不同启动子的总转录活性大大增加,但产生的额外RNA分子较短,在+60位左右终止。IST不是Tat反式激活的RNA靶标(TAR);然而,由于它完全依赖细胞因子发挥活性,IST可能有助于为Tat反式激活提供丰富的RNA靶标,而无需全长病毒mRNA表达。

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