Priano C, Arora R, Jayant L, Mills D R
Health Science Center at Brooklyn, State University of New York, , 450 Clarkson Ave., Brooklyn, NY 11203, USA.
J Mol Biol. 1997 Aug 22;271(3):299-310. doi: 10.1006/jmbi.1997.1194.
We present evidence for translational activation of the Qbeta coliphage maturation cistron, mediated by the presence of Qbeta replicase. This activation does not require RNA replication, translation of a second gene, or any direct protein-RNA binding at the maturation gene initiation site. Our data support a model in which the Qbeta maturation gene remains translationally "off" by two means: (1) the thermodynamic stability of an RNA structure that greatly discourages, but does not eliminate, ribosome access at the maturation start site; and (2) the presence of the stronger, proximal coat gene ribosome binding site. Moreover, maturation gene expression is switched "on" when ribosome entry at the coat initiation site, present on the same polycistronic RNA molecule, is repressed by Qbeta replicase, thereby allowing ribosomes to compete for the weaker, upstream maturation start site.
我们提供了由Qβ复制酶介导的Qβ噬菌体成熟顺反子翻译激活的证据。这种激活不需要RNA复制、第二个基因的翻译,也不需要在成熟基因起始位点有任何直接的蛋白质-RNA结合。我们的数据支持一种模型,其中Qβ成熟基因通过两种方式保持翻译“关闭”状态:(1)一种RNA结构的热力学稳定性极大地阻碍了核糖体进入成熟起始位点,但并未完全消除这种可能性;(2)存在更强的、近端的外壳基因核糖体结合位点。此外,当存在于同一多顺反子RNA分子上的外壳起始位点的核糖体进入被Qβ复制酶抑制时,成熟基因表达被切换为“开启”状态,从而使核糖体能够竞争较弱的上游成熟起始位点。