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纤细裸藻叶绿体基因组“截短的核糖体RNA操纵子”的核苷酸序列。

Nucleotide sequence of a 'truncated rRNA operon' of the Euglena gracilis chloroplast genome.

作者信息

Roux E, Graf L, Stutz E

出版信息

Nucleic Acids Res. 1983 Apr 11;11(7):1957-68. doi: 10.1093/nar/11.7.1957.

Abstract

An extra 16S rRNA gene (s-16S rDNA) from the Euglena gracilis chloroplast genome and several hundred positions of its flanking regions have been sequenced. The structural part has 1486 positions and is to 98% homologous in its sequence with the 16S rRNA gene in functional chloroplast rRNA operons. Sequences of about 200 positions upstream and 15 positions downstream of the structural part of the s-16S rRNA gene region are highly homologous with corresponding parts in the functional operon. Neither tRNA genes (A1a, I1e) nor parts of the 23S and 5S rRNA genes are found within 557 positions after the 3' end of the s-16S rRNA gene, i.e., the 330 bp homology, observed in electron microscopic studies of heteroduplexes (4), between the s-16S rDNA downstream region and the 6.2 kb repeated segment containing the functional rRNA operon, must be due to a DNA stretch in the interoperon spacer. A structural model of the "truncated rRNA operon" is presented. Results from S-1 endonuclease analysis suggest that the s-16S rDNA region is probably not transcribed into stable s-16S rRNA.

摘要

已对来自纤细裸藻叶绿体基因组的一个额外的16S rRNA基因(s - 16S rDNA)及其侧翼区域的数百个位置进行了测序。结构部分有1486个位置,其序列与功能性叶绿体rRNA操纵子中的16S rRNA基因有98%的同源性。s - 16S rRNA基因区域结构部分上游约200个位置和下游15个位置的序列与功能性操纵子中的相应部分高度同源。在s - 16S rRNA基因3'端之后的557个位置内未发现tRNA基因(A1a、I1e)以及23S和5S rRNA基因的部分,即电子显微镜异源双链体研究(4)中观察到的s - 16S rDNA下游区域与包含功能性rRNA操纵子的6.2 kb重复片段之间330 bp的同源性,必定归因于操纵子间间隔区的一段DNA序列。提出了“截短的rRNA操纵子”的结构模型。S - 1核酸内切酶分析结果表明,s - 16S rDNA区域可能不会转录为稳定的s - 16S rRNA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06d8/325853/683a82be8743/nar00352-0019-a.jpg

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