Fisher A G, Ensoli B, Ivanoff L, Chamberlain M, Petteway S, Ratner L, Gallo R C, Wong-Staal F
Science. 1987 Aug 21;237(4817):888-93. doi: 10.1126/science.3497453.
The genome of the human immunodeficiency virus HIV-1 contains at least eight genes, of which three (sor, R, and 3' orf) have no known function. In this study, the role of the sor gene was examined by constructing a series of proviral genomes of HIV-1 that either lacked the coding sequences for sor or contained point mutations in sor. Analysis of four such mutants revealed that although each clone could generate morphologically normal virus particles upon transfection, the mutant viruses were limited in their capacity to establish stable infection. Virus derived from transfection of Cos-1 cells (OKT4-) with sor mutant proviral DNA's was resistant to transmission to OKT4+ "susceptible" cells under cell-free conditions, and was transmitted poorly by coculture. In contrast, virus derived from clones with an intact sor frame was readily propagated by either approach. Normal amounts of gag-, env-, and pol-derived proteins were produced by all four mutants and assays in both lymphoid and nonlymphoid cells indicated that their trans-activating capacity was intact and comparable with wild type. Thus the sor gene, although not absolutely required in HIV virion formation, influences virus transmission in vitro and is crucial in the efficient generation of infectious virus. The data also suggest that sor influences virus replication at a novel, post-translational stage and that its action is independent of the regulatory genes tat and trs.
人类免疫缺陷病毒HIV-1的基因组至少包含八个基因,其中三个基因(sor、R和3'orf)的功能尚不清楚。在本研究中,通过构建一系列HIV-1前病毒基因组来研究sor基因的作用,这些基因组要么缺少sor的编码序列,要么在sor中含有点突变。对四个这样的突变体的分析表明,尽管每个克隆在转染后都能产生形态正常的病毒颗粒,但突变病毒建立稳定感染的能力有限。用sor突变前病毒DNA转染Cos-1细胞(OKT4-)产生的病毒在无细胞条件下对传播到OKT4+“易感”细胞具有抗性,并且通过共培养传播效果不佳。相比之下,来自具有完整sor框架的克隆产生的病毒可以通过任何一种方法轻松传播。所有四个突变体都产生了正常量的gag、env和pol衍生蛋白,并且在淋巴细胞和非淋巴细胞中的检测表明它们的反式激活能力是完整的,并且与野生型相当。因此,sor基因虽然在HIV病毒体形成中不是绝对必需的,但它在体外影响病毒传播,并且在有效产生感染性病毒方面至关重要。数据还表明,sor在一个新的翻译后阶段影响病毒复制,并且其作用独立于调节基因tat和trs。