Peters G, Dahlberg J E
J Virol. 1979 Aug;31(2):398-407. doi: 10.1128/JVI.31.2.398-407.1979.
Initiation of RNA-directed DNA synthesis in virions of Moloney murine leukemia virus requires a cellular tRNAPro as primer. The site(s) on the Moloney murine leukemia virus genome RNA at which functional primer molecules are bound and at which purified tRNAPro hybridizes has been located near (within 20%) the 5' end of the genome. A relatively stable duplex (temperature at which 50% dissociation has occurred, 76 degrees C) is formed between the amino acid acceptor stem of the tRNAPro and a complementary sequence in the Moloney murine leukemia virus 35S RNA. The interaction involves 19 base pairs, extending from the penultimate nucleotide at the 3' end of the tRNAPro but apparently not including the 3'-terminal adenosine residue. In most respects, the interaction between primer and template in Moloney murine leukemia virus parallels the situation in the avian leukosis-sarcoma viruses.
莫洛尼鼠白血病病毒粒子中RNA指导的DNA合成起始需要一种细胞tRNAPro作为引物。已确定功能性引物分子结合的莫洛尼鼠白血病病毒基因组RNA位点以及纯化的tRNAPro杂交的位点位于基因组5'端附近(20%以内)。tRNAPro的氨基酸接受茎与莫洛尼鼠白血病病毒35S RNA中的互补序列之间形成了相对稳定的双链体(发生50%解离的温度为76℃)。这种相互作用涉及19个碱基对,从tRNAPro 3'端倒数第二个核苷酸开始,但显然不包括3'末端腺苷残基。在大多数方面,莫洛尼鼠白血病病毒中引物与模板之间的相互作用与禽白血病-肉瘤病毒的情况相似。