Suppr超能文献

通过缺失人tRNAimet基因中的3' 终止和加工序列在体内和体外生成长期通读转录本。

Generation of long read-through transcripts in vivo and in vitro by deletion of 3' termination and processing sequences in the human tRNAimet gene.

作者信息

Adeniyi-Jones S, Romeo P H, Zasloff M

出版信息

Nucleic Acids Res. 1984 Jan 25;12(2):1101-15. doi: 10.1093/nar/12.2.1101.

Abstract

The effects of 3' deletions of the coding and flanking regions of the human tRNAimet gene on its transcription and subsequent processing have been studied both in vitro and in vivo. We demonstrate that in the absence of the oligo T stop signal, polymerase III will read-through efficiently to the next available downstream stop signal. In mutations preserving the 3' terminal sequence of the coding region these read-through transcripts are efficiently processed, irrespective of their length and sequence by an endonucleolytic cleavage to yield both a mature tRNA and an intact trailer RNA. However, deletions involving the terminal regions up to +62 in the coding sequence produce an unprocessed co-transcript of tRNA and downstream sequences. Deletions further within the B promoter box abolish transcription. The use of these mutants as possible "portable" promoters is discussed.

摘要

已经在体外和体内研究了人tRNAimet基因编码区和侧翼区3'缺失对其转录及后续加工的影响。我们证明,在没有寡聚T终止信号的情况下,聚合酶III将有效地通读至下一个可用的下游终止信号。在保留编码区3'末端序列的突变中,这些通读转录本通过内切核酸酶切割得到有效加工,无论其长度和序列如何,均可产生成熟的tRNA和完整的尾随RNA。然而,编码序列中涉及直至+62的末端区域的缺失会产生未加工的tRNA和下游序列的共转录本。B启动子框内进一步的缺失会消除转录。讨论了将这些突变体用作可能的“便携式”启动子的用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70ab/318559/0db9e1097d84/nar00320-0259-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验