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酵母SUP4-o tRNA基因中一个点突变的多效性效应:酿酒酵母体内前体tRNA加工

Pleiotropic effect of a point mutation in the yeast SUP4-o tRNA gene: in vivo pre-tRNA processing in S. cerevisiae.

作者信息

Wilhelm M L, Keith G, Fix C, Wilhelm F X

机构信息

Institut de Biologie Moléculaire, CNRS, Strasbourg, France.

出版信息

Nucleic Acids Res. 1992 Feb 25;20(4):791-6. doi: 10.1093/nar/20.4.791.

DOI:10.1093/nar/20.4.791
PMID:1542574
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC312019/
Abstract

The expression of mutant tyrosine-inserting ochre suppressor SUP4-o tRNA genes in vivo in S. cerevisiae was examined as a basis for further studies of tRNA transcription and processing. In vivo yeast precursor tRNAs have been identified by filter hybridization and primer extension analysis. We have previously shown that a mutant SUP4-o tRNA gene with a C52----A52 transversion at positive 52 (C52----A52(+IVS) allele) was transcribed but that the primary transcript was not processed correctly. We show here that 5' and 3' end processing as well as splicing are defective for this mutant but that the 5' end processing is restored when the intron is removed from the gene by oligonucleotide directed mutagenesis (C52----A52(-IVS) allele). Our results imply that the C52----A52 transversion by itself cannot account for the lack of susceptibility to RNase P cleavage but that the overall tertiary structure of the mutant tRNA precursor is destabilized by the intron/anticodon stem. A second consequence of the C52----A52 transversion is to prevent complete maturation of the tRNA precursor at its 3' end since intermediates containing incompletely processed 3' trailers accumulate in the yeast cells transformed with the C52----A52(-IVS) allele. A correct structure of the T stem might therefore define a structural feature required for the recognition of the 3' processing activity.

摘要

作为进一步研究tRNA转录和加工的基础,对突变型酪氨酸插入赭石抑制子SUP4-o tRNA基因在酿酒酵母体内的表达进行了检测。通过滤膜杂交和引物延伸分析,已在体内鉴定出酵母前体tRNA。我们先前已表明,在正向52处发生C52→A52颠换的突变型SUP4-o tRNA基因(C52→A52(+IVS)等位基因)能够转录,但初级转录本无法正确加工。我们在此表明,该突变体的5'和3'末端加工以及剪接均存在缺陷,但当通过寡核苷酸定向诱变从基因中去除内含子(C52→A52(-IVS)等位基因)时,5'末端加工得以恢复。我们的结果表明,C52→A52颠换本身不能解释对RNase P切割缺乏敏感性的原因,而是突变型tRNA前体的整体三级结构因内含子/反密码子茎而不稳定。C52→A52颠换的另一个后果是阻止tRNA前体在其3'末端完全成熟,因为在用C52→A52(-IVS)等位基因转化的酵母细胞中积累了含有未完全加工的3'尾的中间体。因此,T茎的正确结构可能定义了识别3'加工活性所需的结构特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f33d/312019/327f6455eda5/nar00078-0149-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f33d/312019/7135e49d1888/nar00078-0148-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f33d/312019/739885e5ed63/nar00078-0148-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f33d/312019/37cb55174754/nar00078-0149-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f33d/312019/327f6455eda5/nar00078-0149-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f33d/312019/7135e49d1888/nar00078-0148-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f33d/312019/739885e5ed63/nar00078-0148-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f33d/312019/37cb55174754/nar00078-0149-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f33d/312019/327f6455eda5/nar00078-0149-b.jpg

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本文引用的文献

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