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一种新型酵母小核仁RNA的鉴定与功能分析。

Identification and functional analysis of a novel yeast small nucleolar RNA.

作者信息

Dandekar T, Tollervey D

机构信息

EMBL, Heidelberg, Germany.

出版信息

Nucleic Acids Res. 1993 Nov 25;21(23):5386-90. doi: 10.1093/nar/21.23.5386.

Abstract

snR31 is a RNA species of 225 nt. which has the trimethyl guanosine cap structure typical of small nuclear RNAs (snRNAs) and yeast small nucleolar RNAs (snoRNAs), and is associated with the nucleolar proteins fibrillarin (NOP1) and GAR1. On sub-nuclear fractionation, snR31 behaves like other snoRNAs, and is enriched in a nucleolar fraction. The SNR31 genomic locus is close to the SNR5 locus, which encodes another snoRNA. The two genes are divergently transcribed with 217 bp separating the transcription start sites. Disruption of the SNR31 gene does not detectably impair growth in a haploid strain. Analyses of pre-rRNA processing in wild-type and snr31- strains shows some accumulation of the 35S primary transcript in the mutant, indicating a mild impairment of the initial steps in pre-rRNA processing.

摘要

snR31是一种225个核苷酸的RNA分子,具有典型的小核RNA(snRNA)和酵母小核仁RNA(snoRNA)的三甲基鸟苷帽结构,并且与核仁蛋白纤维蛋白原(NOP1)和GAR1相关联。在亚核分级分离中,snR31的行为与其他snoRNA相似,并且在核仁级分中富集。SNR31基因座靠近SNR5基因座,后者编码另一种snoRNA。这两个基因以相反方向转录,转录起始位点之间相隔217个碱基对。在单倍体菌株中,SNR31基因的破坏并未检测到对生长有明显损害。对野生型和snr31-菌株中前体rRNA加工的分析表明,突变体中35S初级转录本有一些积累,这表明前体rRNA加工的初始步骤有轻度损害。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6792/310575/5c2068220868/nar00072-0109-a.jpg

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