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人类免疫缺陷病毒1型的nef基因对病毒生长无负面影响。

Lack of a negative influence on viral growth by the nef gene of human immunodeficiency virus type 1.

作者信息

Kim S, Ikeuchi K, Byrn R, Groopman J, Baltimore D

机构信息

Whitehead Institute, Nine Cambridge Center, MA 02142.

出版信息

Proc Natl Acad Sci U S A. 1989 Dec;86(23):9544-8. doi: 10.1073/pnas.86.23.9544.

DOI:10.1073/pnas.86.23.9544
PMID:2687883
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC298533/
Abstract

Human immunodeficiency virus type 1 (HIV-1) contains an open reading frame called nef at the 3' end of its genome. The nef gene product has been reported to down-regulate viral growth by suppressing viral transcription through interaction with the long terminal repeat region. We have compared two isogenic HIV-1 (HIV-1-WI3) strains, one of which lacks nef expression, and found little difference between them in in vitro growth. We tested effects on viral entry, DNA synthesis, and RNA expression by measuring HIV-specific low molecular weight DNA and RNA after infection. The qualitative and quantitative aspects of DNA and RNA synthesis were comparable between the nef+ and nef- strains. The effects on viral growth were also examined by following changes in reverse transcriptase activity during the course of infection. The presence of the nef gene product failed to slow viral growth in several different cell types tested, including the human T-lymphocyte cell lines H9 and CEM-SS, human primary T cells enriched for CD4+ cells, and human monocytic cell lines U-937 and THP-1. On the contrary, the nef+ strain grew more efficiently in some cell types than the nef- strain. The same results were obtained with nef+ and nef- strains of a different virus, HIV-1-432, whose Nef had been reported to have a negative effect on viral growth. Our data suggest that the Nef protein does not act as a negative factor, at least in the experimental systems employed in our studies.

摘要

1型人类免疫缺陷病毒(HIV-1)在其基因组的3'端含有一个名为nef的开放阅读框。据报道,nef基因产物通过与长末端重复序列区域相互作用抑制病毒转录,从而下调病毒生长。我们比较了两种同基因的HIV-1(HIV-1-WI3)毒株,其中一种缺乏nef表达,发现它们在体外生长方面几乎没有差异。我们通过测量感染后HIV特异性低分子量DNA和RNA来测试对病毒进入、DNA合成和RNA表达的影响。nef+和nef-毒株之间DNA和RNA合成的定性和定量方面是可比的。在感染过程中,通过跟踪逆转录酶活性的变化,也研究了对病毒生长的影响。在几种测试的不同细胞类型中,包括人类T淋巴细胞系H9和CEM-SS、富集CD4+细胞的人类原代T细胞以及人类单核细胞系U-937和THP-1,nef基因产物的存在未能减缓病毒生长。相反,在某些细胞类型中,nef+毒株比nef-毒株生长得更有效。对于另一种病毒HIV-1-432的nef+和nef-毒株也得到了相同的结果,其Nef据报道对病毒生长有负面影响。我们的数据表明,至少在我们研究中使用的实验系统中,Nef蛋白不作为负因子起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e718/298533/f9585afdb093/pnas00290-0504-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e718/298533/f0c36baa8ed7/pnas00290-0503-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e718/298533/d1c3be7bc96c/pnas00290-0503-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e718/298533/f9585afdb093/pnas00290-0504-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e718/298533/f0c36baa8ed7/pnas00290-0503-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e718/298533/d1c3be7bc96c/pnas00290-0503-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e718/298533/f9585afdb093/pnas00290-0504-a.jpg

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