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内含子突变影响酿酒酵母SUP53前体tRNA的剪接。

Intron mutations affect splicing of Saccharomyces cerevisiae SUP53 precursor tRNA.

作者信息

Strobel M C, Abelson J

出版信息

Mol Cell Biol. 1986 Jul;6(7):2674-83. doi: 10.1128/mcb.6.7.2674-2683.1986.

Abstract

The Saccharomyces cerevisiae amber suppressor tRNA gene SUP53 (a tRNALeu3 allele) was used to investigate the role of intron structure and sequence on precursor tRNA splicing in vivo and in vitro. This gene encodes a pre-tRNA which contains a 32-base intervening sequence. Two types of SUP53 intron mutants were constructed: ones with an internal deletion of the natural SUP53 intron and ones with a novel intron. These mutant genes were transcribed in vitro, and the end-processed transcripts were analyzed for their ability to serve as substrates for the partially purified S. cerevisiae tRNA endonuclease and ligase. The in vitro phenotype of these mutant RNAs was correlated with the in vivo suppressor tRNA function of these SUP53 alleles after integration of the genes into the yeast genome. Analysis of these mutant pre-tRNAs, which exhibited no perturbation of the mature domain, clearly showed that intron structure and sequence can have profound effects on pre-tRNA splicing. All of the mutant RNAs, which were inefficiently spliced or unspliced, evidenced cleavage only at the 5' splice junction. Base changes in the intron proximal to the 3' splice junction could partially rescue the splicing defect. The implications of these data for tRNA endonuclease-substrate interactions are discussed.

摘要

酿酒酵母琥珀抑制tRNA基因SUP53(一种tRNALeu3等位基因)被用于研究内含子结构和序列在体内和体外对前体tRNA剪接的作用。该基因编码一种前体tRNA,其含有一个32个碱基的间隔序列。构建了两种类型的SUP53内含子突变体:一种是天然SUP53内含子内部缺失的突变体,另一种是含有新内含子的突变体。这些突变基因在体外进行转录,并对末端加工后的转录本作为部分纯化的酿酒酵母tRNA内切核酸酶和连接酶底物的能力进行分析。在将这些基因整合到酵母基因组后,这些突变RNA的体外表型与这些SUP53等位基因的体内抑制tRNA功能相关。对这些未表现出成熟结构域扰动的突变前体tRNA的分析清楚地表明,内含子结构和序列可对前体tRNA剪接产生深远影响。所有低效剪接或未剪接的突变RNA仅在5'剪接位点处有切割。3'剪接位点近端内含子中的碱基变化可部分挽救剪接缺陷。讨论了这些数据对tRNA内切核酸酶 - 底物相互作用的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b490/367824/5ad2a1913a1c/molcellb00091-0398-a.jpg

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