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18S核糖体RNA的合成需要U3与核糖体前体RNA之间的碱基配对。

Base pairing between U3 and the pre-ribosomal RNA is required for 18S rRNA synthesis.

作者信息

Beltrame M, Tollervey D

机构信息

Gene Expression Programme, European Molecular Biology Laboratory, Heidelberg, Germany.

出版信息

EMBO J. 1995 Sep 1;14(17):4350-6. doi: 10.1002/j.1460-2075.1995.tb00109.x.

Abstract

The nucleolus, the site of pre-ribosomal RNA (pre-rRNA) synthesis and processing in eukaryotic cells, contains a number of small nucleolar RNAs (snoRNAs). Yeast U3 snoRNA is required for the processing of 18S rRNA from larger precursors and contains a region complementary to the pre-rRNA. Substitution mutations in the pre-rRNA which disrupt this base pairing potential are lethal and prevent synthesis of 18S rRNA. These mutant pre-rRNAs show defects in processing which closely resemble the effects of genetic depletion of components of the U3 snoRNP. Co-expression of U3 snoRNAs which carry compensatory mutations allows the mutant pre-rRNAs to support viability and synthesize 18S rRNA at high levels. Pre-rRNA processing steps which are blocked by the external transcribed spacer region mutations are largely restored by expression of the compensatory U3 mutants. Pre-rRNA processing therefore requires direct base pairing between snoRNA and the substrate. Base pairing with the substrate is thus a common feature of small RNAs involved in mRNA and rRNA maturation.

摘要

核仁是真核细胞中核糖体前体RNA(pre-rRNA)合成与加工的场所,含有多种小分子核仁RNA(snoRNA)。酵母U3 snoRNA是从较大前体加工生成18S rRNA所必需的,并且包含一个与pre-rRNA互补的区域。pre-rRNA中的取代突变若破坏这种碱基配对潜能则是致死性的,并会阻止18S rRNA的合成。这些突变的pre-rRNA在加工过程中表现出缺陷,这与U3 snoRNP组分的基因缺失效应极为相似。携带补偿性突变的U3 snoRNA的共表达可使突变的pre-rRNA支持细胞存活并高水平合成18S rRNA。由外部转录间隔区突变所阻断的pre-rRNA加工步骤在很大程度上可通过补偿性U3突变体的表达得以恢复。因此,pre-rRNA加工需要snoRNA与底物之间直接的碱基配对。与底物的碱基配对因此是参与mRNA和rRNA成熟的小RNA的一个共同特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fba/394519/a2d4197ac24b/emboj00041-0239-a.jpg

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