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U3小核仁RNA的高度保守元件与小核糖体亚基RNA之间的功能性碱基配对相互作用。

Functional base-pairing interaction between highly conserved elements of U3 small nucleolar RNA and the small ribosomal subunit RNA.

作者信息

Hughes J M

机构信息

Department of Biochemistry, University of Liverpool, UK.

出版信息

J Mol Biol. 1996 Jun 21;259(4):645-54. doi: 10.1006/jmbi.1996.0346.

DOI:10.1006/jmbi.1996.0346
PMID:8683571
Abstract

The U3 nucleolar RNA has a remarkably wide phyletic distribution extending from the Eukarya to the Archaea. It functions in maturation of the small subunit (SSU) rRNA through a mechanism which is as yet unknown but which involves base-pairing with pre-rRNA. The most conserved part of U3 is within 30 nucleotides of the 5' end, but as yet no function for this domain has been proposed. Elements within this domain are complementary to highly conserved sequences in the SSU rRNA which, in the mature form, fold into a universally conserved pseudoknot. The nature of the complementarity suggests a novel mechanism for U3 function whereby U3 facilitates correct folding of the pseudoknot. Wide phylogenetic comparison provides compelling evidence in support of the interaction in that significant complementary changes have taken place, particularly in the archaeon Sulfolobus, which maintain the base-pairing. Base-substitution mutations in yeast U3 designed to disrupt the base-pairing indicate that the interaction is probably essential. These include cold-sensitivity mutations which exhibit phenotypes similar to U3-depletion, but without impairment of the AO processing step, which occurs within the 5' ETS. These phenotypes are consistent with the destabilization of SSU precursors and partial impairment of the processing steps A1, at the 5' ETS/18 S boundary, and A2, within the ITS1.

摘要

U3核仁RNA具有非常广泛的系统发育分布,从真核生物延伸到古细菌。它通过一种尚不清楚的机制在小亚基(SSU)rRNA的成熟过程中发挥作用,但该机制涉及与前体rRNA的碱基配对。U3最保守的部分在5'端的30个核苷酸内,但尚未有人提出该结构域的功能。该结构域内的元件与SSU rRNA中的高度保守序列互补,成熟形式的这些序列折叠成一个普遍保守的假结。互补性的本质提示了一种U3功能的新机制,即U3促进假结的正确折叠。广泛的系统发育比较提供了有力证据支持这种相互作用,因为发生了显著的互补性变化,特别是在古细菌嗜热栖热菌中,这些变化维持了碱基配对。酵母U3中旨在破坏碱基配对的碱基替代突变表明这种相互作用可能是必不可少的。这些包括冷敏突变,其表现出与U3缺失相似的表型,但不影响发生在5'ETS内的AO加工步骤。这些表型与SSU前体不稳定以及在5'ETS/18 S边界处的加工步骤A1和ITS1内的加工步骤A2的部分受损一致。

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