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高等植物线粒体中的RNA剪接:通过电穿孔小麦线粒体中的嵌合细胞色素c氧化酶亚基II基因确定II类内含子中的功能元件。

RNA splicing in higher plant mitochondria: determination of functional elements in group II intron from a chimeric cox II gene in electroporated wheat mitochondria.

作者信息

Farré Jean-Claude, Araya Alejandro

机构信息

Laboratoire de Réplication et Expression des Gènes Eucaryotes et Rétroviraux, UMR 5097, Centre National de la Recherche Scientifique and Université Victor Segalen-Bordeaux II. 146, rue Leo Saignat. 33076 Bordeaux Cedex, France.

出版信息

Plant J. 2002 Jan;29(2):203-13. doi: 10.1046/j.1365-313x.2002.01207.x.

Abstract

Higher plant mitochondria mainly contain group II introns presenting a secondary structure with six helical domains linked to a central hub. Experimental evidence of functional elements in higher plant mitochondria introns is limited since they are unable to undergo self-splicing and the definition of functional domains is based on data obtained from yeast autocatalytic introns. Here we study the role of putative functional elements required for the splicing reaction. The exon-binding and intron-binding sites (EBS and IBS, respectively), and the domain 6, which is involved in lariat formation, were analysed by site-directed mutagenesis and transient expression in electroporated mitochondria. The data presented here demonstrate the role of EBS1-IBS1 and EBS2-IBS2 interactions and reveal a new secondary-structure interaction. The role of the C to U editing conversion in the IBS1 motif is discussed.

摘要

高等植物线粒体主要包含II类内含子,其呈现出一种二级结构,该结构具有六个与中心枢纽相连的螺旋结构域。由于高等植物线粒体内含子无法进行自我剪接,且功能域的定义基于从酵母自催化内含子获得的数据,因此关于高等植物线粒体内含子中功能元件的实验证据有限。在此,我们研究了剪接反应所需的假定功能元件的作用。通过定点诱变和电穿孔线粒体中的瞬时表达,分析了外显子结合位点和内含子结合位点(分别为EBS和IBS)以及参与套索形成的结构域6。本文给出的数据证明了EBS1-IBS1和EBS2-IBS2相互作用的作用,并揭示了一种新的二级结构相互作用。还讨论了IBS1基序中C到U编辑转换的作用。

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