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腺病毒E1A 13S蛋白对在腺病毒载体中表达的人类免疫缺陷病毒长末端重复序列的反式激活作用。

Trans-activation of the human immunodeficiency virus long terminal repeat sequences, expressed in an adenovirus vector, by the adenovirus E1A 13S protein.

作者信息

Rice A P, Mathews M B

机构信息

Cold Spring Harbor Laboratory, NY 11724.

出版信息

Proc Natl Acad Sci U S A. 1988 Jun;85(12):4200-4. doi: 10.1073/pnas.85.12.4200.

Abstract

The human immunodeficiency virus 1 (HIV-1) long terminal repeat (LTR) sequences were inserted into adenovirus in place of the E1 region. The HIV-1 LTR contained in this recombinant adenovirus responds to trans-activation by tatIII in a HeLa cell line constitutively expressing that HIV-1 gene product. In addition, the HIV-1 LTR is activated by the adenovirus E1A 13S, but not 12S or 9S, gene product when it is supplied in trans by a coinfecting wild-type adenovirus. The Rous sarcoma virus LTR, in a similar recombinant adenovirus, is insensitive to tatIII but is also trans-activated by the E1A 13S protein. The action of the 13S E1A and tatIII proteins are additive for the HIV-1 LTR in the context of adenovirus and they appear to act at the transcriptional level. As in HeLa cells, the adenovirus-borne HIV-1 LTR is inactive in the absence of a trans-activator in H9 and Jurkat cells, two human leukemic T-cell lines. This suggests that recombinant adenoviruses have diagnostic potential for the detection of trans-activators of the HIV-1 LTR that are present in circulating human lymphocytes.

摘要

人类免疫缺陷病毒1型(HIV-1)的长末端重复序列(LTR)被插入到腺病毒的E1区域。这种重组腺病毒中所含的HIV-1 LTR在持续表达HIV-1基因产物的HeLa细胞系中对tatIII的反式激活有反应。此外,当通过共感染野生型腺病毒反式提供时,HIV-1 LTR被腺病毒E1A 13S基因产物激活,但不被12S或9S基因产物激活。在类似的重组腺病毒中,劳氏肉瘤病毒LTR对tatIII不敏感,但也被E1A 13S蛋白反式激活。在腺病毒的背景下,13S E1A和tatIII蛋白对HIV-1 LTR的作用是相加的,并且它们似乎在转录水平起作用。与在HeLa细胞中一样,在两种人类白血病T细胞系H9和Jurkat细胞中,腺病毒携带的HIV-1 LTR在没有反式激活剂的情况下是无活性的。这表明重组腺病毒对于检测循环人类淋巴细胞中存在的HIV-1 LTR反式激活剂具有诊断潜力。

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