Hernández Greco
Department of Biology, McGill University, 1205 Dr. Penfield, Montreal, QC. H3A 1B1, Canada.
Trends Biochem Sci. 2009 Apr;34(4):166-75. doi: 10.1016/j.tibs.2009.02.001. Epub 2009 Mar 18.
The Shine-Dalgarno sequence of prokaryotic mRNAs, which helps to bind and position the ribosome at the start site for protein synthesis, is absent from eukaryotic mRNAs. Instead, for most, a structure at the 5' end and a much larger number of protein initiation factors are needed for both binding of the ribosome and for successful start-site selection, that is, a 'cap-dependent' initiation mechanism. Although the mechanics of this process are well studied, what is not clear is how it evolved. By analyzing recent progress in different fields, I suggest that it was the need to adjust to the arrival of the nuclear membrane and the subsequent requirement to export intron-less mRNAs to the cytoplasm that spurred the shift to the more complex translation initiation mechanism in eukaryotes.
原核生物信使核糖核酸(mRNA)的夏因-达尔加诺序列有助于在蛋白质合成起始位点结合并定位核糖体,而真核生物mRNA中不存在该序列。相反,对于大多数真核生物mRNA而言,核糖体结合及成功选择起始位点都需要5'端的一个结构以及大量蛋白质起始因子,即一种“帽依赖型”起始机制。尽管这一过程的机制已得到充分研究,但尚不清楚的是它是如何进化的。通过分析不同领域的最新进展,我认为是适应核膜的出现以及随后将无内含子mRNA输出到细胞质的需求,促使真核生物转向了更复杂的翻译起始机制。