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非编码DNA序列在酵母tRNA转录和加工中的作用。

The role of non-coding DNA sequences in transcription and processing of a yeast tRNA.

作者信息

Raymond G J, Johnson J D

出版信息

Nucleic Acids Res. 1983 Sep 10;11(17):5969-88. doi: 10.1093/nar/11.17.5969.

Abstract

We have tested the hypothesis that conserved sequences in the intervening sequence (IVS) and 5'-flanking region of a yeast tRNALeu3 gene serve some function. Genes with deletions of 8, 10, 13 and 20 bp in the IVS are all active as templates in vitro. Yeast extracts produce mature tRNALeu3 from delta 8, delta 10 and delta 13 genes. Xenopus extracts do not detectably ligate the 5' and 3' half-molecules resulting from IVS excision. Neither extract is able to excise the IVS from delta 20 precursors. Genes with introns enlarged by 10, 21 or 30 bp of DNA produce mature tRNA. Insertion of 103 bp results in reduced levels of transcription, little if any end maturation, and no detectable mature product. A conserved 15 bp sequence is present at the 5'-end of the tRNA sequence. Replacement of yeast DNA up to position -22 leaves the tRNA gene transcriptionally active. With replacement extended to -2 the gene is active in Xenopus extracts but nearly inert in yeast extracts. We conclude that tRNA transcription in yeast is insensitive to IVS structure but can be positively influenced by 5'-flanking sequence.

摘要

我们已经验证了这样一个假说

酵母tRNALeu3基因的间隔序列(IVS)和5'侧翼区域中的保守序列具有某种功能。IVS中缺失8、10、13和20个碱基对的基因在体外均作为模板具有活性。酵母提取物可从δ8、δ10和δ13基因产生成熟的tRNALeu3。非洲爪蟾提取物无法检测到由IVS切除产生的5'和3'半分子的连接。两种提取物都不能从δ20前体中切除IVS。内含子通过10、21或30个碱基对的DNA扩增的基因可产生成熟的tRNA。插入103个碱基对会导致转录水平降低,几乎没有末端成熟,并且没有可检测到的成熟产物。在tRNA序列的5'端存在一个保守的15个碱基对的序列。将酵母DNA替换至-22位置时,tRNA基因仍具有转录活性。当替换延伸至-2时,该基因在非洲爪蟾提取物中具有活性,但在酵母提取物中几乎无活性。我们得出结论,酵母中的tRNA转录对IVS结构不敏感,但可受到5'侧翼序列的正向影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8185/326330/38a059fcc839/nar00362-0186-a.jpg

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