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植物锥虫 Phytomonas serpens 动质体线粒体中 mRNA 编辑及引导 RNA 基因定位的证明

Demonstration of mRNA editing and localization of guide RNA genes in kinetoplast-mitochondria of the plant trypanosomatid Phytomonas serpens.

作者信息

Maslov D A, Hollar L, Haghighat P, Nawathean P

机构信息

Department of Biology, University of California, Riverside 92521, USA.

出版信息

Mol Biochem Parasitol. 1998 Jun 1;93(2):225-36. doi: 10.1016/s0166-6851(98)00028-0.

Abstract

Maxicircle molecules of kDNA in several isolates of Phytomonas were detected by hybridization with the 12S rRNA gene probe from Leishmania tarentolae. The estimated size of maxicircles is isolate-specific and varies from 27 to 36 kb. Fully edited and polyadenylated mRNA for kinetoplast-encoded ribosomal protein S12 (RPS12) was found in the steady-state kinetoplast RNA isolated from Phytomonas serpens strain 1G. Two minicircles (1.45 kb) from this strain were also sequenced. Each minicircle contains two 120 bp conserved regions positioned 180 degrees apart, a region enriched with G and T bases and a variable region. One minicircle encodes a gRNA for the first block of editing of RPSl2 mRNA, and the other encodes a gRNA with unknown function. A gRNA gene for the second block of RPSl2 was found on a minicircle sequenced previously. On each minicircle, a gRNA gene is located in the variable region in a similar position and orientation with respect to the conserved regions.

摘要

通过与来自热带利什曼原虫的12S rRNA基因探针杂交,在几种植滴虫分离株中检测到了kDNA的大环分子。大环的估计大小因分离株而异,范围从27至36 kb。在从植滴虫1G菌株分离的稳态动质体RNA中发现了动质体编码的核糖体蛋白S12(RPS12)的完全编辑和多聚腺苷酸化的mRNA。还对该菌株的两个小环(1.45 kb)进行了测序。每个小环包含两个相距180度定位的120 bp保守区域、一个富含G和T碱基的区域以及一个可变区域。一个小环编码用于RPSl2 mRNA第一编辑块的引导RNA(gRNA),另一个编码功能未知的gRNA。在先前测序的一个小环上发现了RPSl2第二编辑块的gRNA基因。在每个小环上,一个gRNA基因位于可变区域中相对于保守区域的相似位置和方向。

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