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从一种RNA病毒基因组中缺失的发夹结构的进化重建。

Evolutionary reconstruction of a hairpin deleted from the genome of an RNA virus.

作者信息

Olsthoorn R C, van Duin J

机构信息

Department of Biochemistry, Leiden Institute of Chemistry, Gorlaeus Laboratories, University of Leiden, The Netherlands.

出版信息

Proc Natl Acad Sci U S A. 1996 Oct 29;93(22):12256-61. doi: 10.1073/pnas.93.22.12256.

Abstract

The intercistronic region between the maturation and coat-protein genes of RNA phage MS2 contains important regulatory and structural information. The sequence participates in two adjacent stem-loop structures, one of which, the coat-initiator hairpin, controls coat-gene translation and is thus under strong selection pressure. We have removed 19 out of the 23 nucleotides constituting the intercistronic region, thereby destroying the capacity of the phage to build the two hairpins. The deletion lowered coat-protein yield more than 1000-fold, and the titer of the infectious clone carrying the deletion dropped 10 orders of magnitude as compared with the wild type. Two types of revertants were recovered. One had, in two steps, recruited 18 new nucleotides that served to rebuild the two hairpins and the lost Shine-Dalgarno sequence. The other type had deleted an additional six nucleotides, which allowed the reconstruction of the Shine-Dalgarno sequence and the initiator hairpin, albeit by sacrificing the remnants of the other stem-loop. The results visualize the immense genetic repertoire created by, what appears as, random RNA recombination. It would seem that in this genetic ensemble every possible new RNA combination is represented.

摘要

RNA噬菌体MS2的成熟基因和外壳蛋白基因之间的基因间区域包含重要的调控和结构信息。该序列参与两个相邻的茎环结构,其中一个是外壳起始发夹,它控制着外壳基因的翻译,因此处于强烈的选择压力之下。我们去除了构成基因间区域的23个核苷酸中的19个,从而破坏了噬菌体构建这两个发夹的能力。这种缺失使外壳蛋白产量降低了1000倍以上,与野生型相比,携带该缺失的感染性克隆的滴度下降了10个数量级。我们获得了两种类型的回复突变体。一种通过两个步骤招募了18个新核苷酸,用于重建这两个发夹和丢失的Shine-Dalgarno序列。另一种类型又删除了另外6个核苷酸,这使得Shine-Dalgarno序列和起始发夹得以重建,尽管牺牲了另一个茎环的残余部分。这些结果展示了由看似随机的RNA重组所创造的巨大遗传库。在这个遗传集合中,似乎每种可能的新RNA组合都有代表。

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