Ahmad N, Venkatesan S
Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892.
Science. 1988 Sep 16;241(4872):1481-5. doi: 10.1126/science.3262235.
In studies of the genetics of human immunodeficiency virus type 1 (HIV-1), the product of the nef gene, formerly known as F, 3'-orf, or B-ORF, was a negative regulator of HIV-1 replication. Proviruses with mutations in the nef gene replicated better than their standard counterparts during transient expression, and the mutant virus maintained its enhanced replication even after serial passages in T lymphocytes. The nef protein trans-suppressed, in a dose-dependent manner, the replication of wild-type and nef mutant proviruses and the expression of reporter genes linked to the HIV-1 long terminal repeat (LTR). The repression induced by the nef protein was mediated by inhibition of transcription from the HIV-1 LTR, which contains a far upstream cis element (previously recognized to be a negative regulatory element) between 340 and 156 nucleotides upstream of the RNA initiation site.
在对1型人类免疫缺陷病毒(HIV-1)遗传学的研究中,nef基因的产物,以前称为F、3'-orf或B-ORF,是HIV-1复制的负调节因子。在瞬时表达期间,nef基因发生突变的原病毒比其标准对应物复制得更好,并且即使在T淋巴细胞中连续传代后,突变病毒仍保持其增强的复制能力。nef蛋白以剂量依赖的方式反式抑制野生型和nef突变原病毒的复制以及与HIV-1长末端重复序列(LTR)相连的报告基因的表达。nef蛋白诱导的抑制作用是通过抑制HIV-1 LTR的转录介导的,该LTR在RNA起始位点上游340至156个核苷酸之间含有一个远上游顺式元件(以前被认为是一个负调节元件)。