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海胆线粒体核糖体RNA和信使RNA相互排斥的合成途径。

Mutually exclusive synthetic pathways for sea urchin mitochondrial rRNA and mRNA.

作者信息

Elliott D J, Jacobs H T

机构信息

Department of Genetics, University of Glasgow, United Kingdom.

出版信息

Mol Cell Biol. 1989 Mar;9(3):1069-82. doi: 10.1128/mcb.9.3.1069-1082.1989.

Abstract

The structure and abundance of mitochondrial transcripts in sea urchin embryos were investigated by a combination of RNA blot-hybridization, S1 mapping, and primer extension assays. Between the egg and blastula stages, the relative abundance of mitochondrial rRNAs declined slightly, while that of mitochondrial mRNAs increased up to 10-fold. Fine mapping of the termini of the rRNAs and of the adjacent transcripts indicated that, although they appeared to be butt-joined at their 5' ends to the upstream transcripts, tRNA-Phe 5' to the small subunit (12S) rRNA and NADH dehydrogenase subunit 2 mRNA 5' to the large subunit (16S) rRNA, respectively, their 3' ends were found to overlap the 5' ends of the downstream transcripts. 12S rRNA was found to extend 7 to 13 nucleotides into the sequence of tRNA-Glu; 16S rRNA was shown to terminate 3 to 5 nucleotides inside the coding region of cytochrome oxidase subunit 1 (COI) and 8 to 10 nucleotides from the mapped 5' end of COI mRNA. The rRNAs and the downstream transcripts must therefore be synthesized by distinct pathways, either by alternative processing of the same primary transcript(s) or by processing of different precursors. In either case, the events which select the ribosomal 3' ends preclude the production of functional transcripts of the downstream genes from the same precursor molecule. No developmental alterations in transcript structure were detected. We propose that mitochondrial RNA levels are regulated in early development by the selection of alternate and mutually exclusive RNA-processing pathways.

摘要

通过RNA印迹杂交、S1作图和引物延伸分析相结合的方法,研究了海胆胚胎中线粒体转录本的结构和丰度。在卵和囊胚阶段之间,线粒体rRNA的相对丰度略有下降,而线粒体mRNA的相对丰度增加了10倍。对rRNA末端和相邻转录本的精细作图表明,尽管它们在5'端似乎与上游转录本对接,分别是小亚基(12S)rRNA 5'端的tRNA-Phe和大亚基(16S)rRNA 5'端的NADH脱氢酶亚基2 mRNA,但发现它们的3'端与下游转录本的5'端重叠。发现12S rRNA延伸到tRNA-Glu序列中7至13个核苷酸;16S rRNA显示在细胞色素氧化酶亚基1(COI)的编码区内3至5个核苷酸处终止,距离COI mRNA的定位5'端8至10个核苷酸。因此,rRNA和下游转录本必须通过不同的途径合成,要么通过对同一初级转录本的交替加工,要么通过对不同前体的加工。在任何一种情况下,选择核糖体3'端的事件都会阻止同一前体分子产生下游基因的功能性转录本。未检测到转录本结构的发育变化。我们提出,线粒体RNA水平在早期发育中通过选择交替且相互排斥的RNA加工途径来调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6f0/362697/7354abf3f3e0/molcellb00051-0206-a.jpg

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