Rice A P, Mathews M B
Cold Spring Harbor Laboratory, NY 11724.
Proc Natl Acad Sci U S A. 1988 Jun;85(12):4200-4. doi: 10.1073/pnas.85.12.4200.
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.
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。