Laughrea M, Jetté L
McGill AIDS Centre, Lady Davis Institute for Medical Research, Sir Mortimer B. Davis-Jewish General Hospital, Montreal, Quebec, Canada.
Biochemistry. 1994 Nov 15;33(45):13464-74. doi: 10.1021/bi00249a035.
The genome of all retroviruses, including human immunodeficiency virus type 1 (HIV-1), consists of two identical RNAs noncovalently linked near their 5' end. Dimerization of genomic RNA is thought to modulate several steps in the retroviral life cycle, such as recombination, translation, and encapsidation. We report the results of experiments designed to identify the 5' and 3' boundaries of the dimerization domain of the HIV-1 genome: (1) An HIV-1 RNA starting at nucleotide 252 or at other downstream positions (four tested) does not dimerize despite the inclusion of the whole of a previously proposed dimerization domain (nucleotides 295-401); (2) an RNA starting between nucleotides 242 and 249 (five positions tested) dimerizes to a variable extent depending on the starting position; (3) an RNA starting at nucleotide 233 or at other upstream positions (five tested) is fully or > 80% dimeric; (4) an RNA starting at nucleotide 1 but lacking the 233-251 or the 242-251 region is, respectively, fully monomeric or about 50% monomeric; (5) the 343-401 region contains two strings of G's (GGGGG367 and GGG384) that had been postulated to promote genome dimerization through the formation of guanine quartets. We have deleted the 379-401, 358-401, and 343-401 regions from otherwise dimeric RNAs without changing their ability to dimerize. We reach three conclusions: (1) a dimerization signal exists upstream of the major 5' splice donor (nucleotide 290); (2) the previously proposed downstream dimerization domain is insufficient to promote dimerization and has a 3' half that is not necessary to obtain fully dimeric RNAs; (3) the 5' boundary of the HIV-1 dimerization domain is located somewhere between nucleotides 233 and 242, and the 3' boundary is located no farther than at nucleotide 342, making it possible that the 5' and 3' boundaries of the HIV-1 dimerization domain are both located within the leader sequence. We speculate that the 248-270 or 233-285 region forms a hairpin that is the core dimerization domain of HIV-1 RNA.
所有逆转录病毒的基因组,包括1型人类免疫缺陷病毒(HIV-1),都由两条相同的RNA组成,它们在5'端附近通过非共价键相连。基因组RNA的二聚化被认为可调节逆转录病毒生命周期中的多个步骤,如重组、翻译和衣壳化。我们报告了旨在确定HIV-1基因组二聚化结构域5'和3'边界的实验结果:(1)起始于核苷酸252或其他下游位置(测试了四个位置)的HIV-1 RNA,尽管包含了先前提出的整个二聚化结构域(核苷酸295 - 401),但并未发生二聚化;(2)起始于核苷酸242和249之间(测试了五个位置)的RNA会根据起始位置不同程度地发生二聚化;(3)起始于核苷酸233或其他上游位置(测试了五个位置)的RNA完全或>80%呈二聚体形式;(4)起始于核苷酸1但缺失233 - 251或242 - 251区域的RNA,分别完全呈单体形式或约50%呈单体形式;(5)343 - 401区域包含两串G(GGGGG367和GGG384),据推测它们通过形成鸟嘌呤四联体促进基因组二聚化。我们从原本呈二聚体形式的RNA中删除了379 - 401、358 - 401和343 - 401区域,而不改变它们二聚化的能力。我们得出三个结论:(1)在主要5'剪接供体(核苷酸290)上游存在一个二聚化信号;(2)先前提出的下游二聚化结构域不足以促进二聚化,并且其3'半部分对于获得完全二聚化的RNA并非必需;(3)HIV-1二聚化结构域的5'边界位于核苷酸233和242之间的某个位置,3'边界不超过核苷酸342,这使得HIV-1二聚化结构域的5'和3'边界都有可能位于前导序列内。我们推测248 - 270或233 - 285区域形成一个发夹结构,它是HIV-1 RNA的核心二聚化结构域。