Jain C, Kleckner N
Department of Biochemistry and Molecular Biology, Harvard University, Cambridge, Massachusetts 02138.
Mol Microbiol. 1993 Jul;9(2):233-47. doi: 10.1111/j.1365-2958.1993.tb01686.x.
Translation of the IS10 transposase gene is known to be very infrequent. We have identified mutations whose genetic properties suggest that they act directly to increase or decrease the intrinsic level of translation initiation. Also, we have analysed in detail the effects of these mutations on IS10 mRNA using one particular IS10 derivative. In this case, increases or decreases in translation are accompanied by increases or decreases in both the steady state level and the half-life of transposase mRNA; effects on steady state levels are much more dramatic than effects on message half-life. At wild-type levels of translation initiation, the rate-limiting step in physical decay of full length IS10 message for a particular IS10 derivative is shown to be rne-dependent endonucleolytic cleavage; 3' exonucleases appear to play a secondary role, degrading primary cleavage products. Analysis of interplay between translation mutations and rne function, together with the above observations, suggests that translation stabilizes messages in a general way against rne-dependent endonucleolytic cleavage, and that significant protection may be conferred by one or a few ribosomes. However, dramatic effects of translation on steady state message levels are still observed in an rne mutant and involve the 3' end of the transcript; we propose that these additional effects reflect translation-mediated stimulation of transcript release.
已知IS10转座酶基因的翻译非常罕见。我们已经鉴定出一些突变,其遗传特性表明它们直接作用于增加或降低翻译起始的内在水平。此外,我们使用一种特定的IS10衍生物详细分析了这些突变对IS10 mRNA的影响。在这种情况下,翻译的增加或减少伴随着转座酶mRNA稳态水平和半衰期的增加或减少;对稳态水平的影响比对信息半衰期的影响更为显著。在野生型翻译起始水平下,对于一种特定的IS10衍生物,全长IS10信息物理衰变的限速步骤显示为依赖rne的内切核酸酶切割;3'外切核酸酶似乎起次要作用,降解初级切割产物。翻译突变与rne功能之间相互作用的分析以及上述观察结果表明,翻译以一种普遍的方式稳定信息以抵抗依赖rne的内切核酸酶切割,并且一个或几个核糖体可能提供显著的保护作用。然而,在rne突变体中仍然观察到翻译对稳态信息水平的显著影响,并且涉及转录本的3'末端;我们提出这些额外的影响反映了翻译介导的转录本释放刺激。