Wills N M, Gesteland R F, Atkins J F
Howard Hughes Medical Institute, University of Utah, Salt Lake City 84112.
Proc Natl Acad Sci U S A. 1991 Aug 15;88(16):6991-5. doi: 10.1073/pnas.88.16.6991.
Approximately 5% of the ribosomes translating the gag gene of murine leukemia viruses read through the UAG terminator and translate the in-frame pol gene to produce the gag-pol fusion polyprotein, the sole source of the pol gene products. We show that a pseudoknot located eight nucleotides 3' of the UAG codon in the Moloney murine leukemia virus is required for read-through. This requirement is markedly different from that known to be involved in other cases of read-through but surprisingly similar to some stimulatory sequences known to promote ribosomal frameshifting.
在翻译鼠白血病病毒gag基因的核糖体中,约5%会通读UAG终止密码子,并翻译读码框内的pol基因,以产生gag-pol融合多蛋白,这是pol基因产物的唯一来源。我们发现,莫洛尼鼠白血病病毒中位于UAG密码子3'端八个核苷酸处的假结是通读所必需的。这一需求与已知的其他通读情况明显不同,但令人惊讶的是,它与一些已知能促进核糖体移码的刺激序列相似。