Petrov Anton S, Gulen Burak, Norris Ashlyn M, Kovacs Nicholas A, Bernier Chad R, Lanier Kathryn A, Fox George E, Harvey Stephen C, Wartell Roger M, Hud Nicholas V, Williams Loren Dean
School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, GA 30332;
Department of Biology and Biochemistry, University of Houston, Houston, TX, 77204;
Proc Natl Acad Sci U S A. 2015 Dec 15;112(50):15396-401. doi: 10.1073/pnas.1509761112. Epub 2015 Nov 30.
We present a molecular-level model for the origin and evolution of the translation system, using a 3D comparative method. In this model, the ribosome evolved by accretion, recursively adding expansion segments, iteratively growing, subsuming, and freezing the rRNA. Functions of expansion segments in the ancestral ribosome are assigned by correspondence with their functions in the extant ribosome. The model explains the evolution of the large ribosomal subunit, the small ribosomal subunit, tRNA, and mRNA. Prokaryotic ribosomes evolved in six phases, sequentially acquiring capabilities for RNA folding, catalysis, subunit association, correlated evolution, decoding, energy-driven translocation, and surface proteinization. Two additional phases exclusive to eukaryotes led to tentacle-like rRNA expansions. In this model, ribosomal proteinization was a driving force for the broad adoption of proteins in other biological processes. The exit tunnel was clearly a central theme of all phases of ribosomal evolution and was continuously extended and rigidified. In the primitive noncoding ribosome, proto-mRNA and the small ribosomal subunit acted as cofactors, positioning the activated ends of tRNAs within the peptidyl transferase center. This association linked the evolution of the large and small ribosomal subunits, proto-mRNA, and tRNA.
我们使用三维比较方法,提出了一个关于翻译系统起源与进化的分子水平模型。在这个模型中,核糖体通过累积进化,递归地添加扩展片段,不断生长、吸纳并固定核糖体RNA(rRNA)。通过将祖先核糖体中扩展片段的功能与其在现存核糖体中的功能相对应,来确定这些扩展片段的功能。该模型解释了核糖体大亚基、小亚基、转运RNA(tRNA)和信使RNA(mRNA)的进化过程。原核生物核糖体分六个阶段进化,依次获得RNA折叠、催化、亚基结合、协同进化、解码、能量驱动转位和表面蛋白化的能力。真核生物特有的另外两个阶段导致了类似触手状的rRNA扩展。在这个模型中,核糖体蛋白化是蛋白质在其他生物过程中广泛应用的驱动力。出口通道显然是核糖体进化各阶段的核心主题,并不断扩展和加固。在原始的非编码核糖体中,原始mRNA和小核糖体亚基作为辅助因子,将tRNA的活化末端定位在肽基转移酶中心内。这种关联将核糖体大亚基和小亚基、原始mRNA和tRNA的进化联系了起来。