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布氏锥虫线粒体的核糖核酸内切酶活性

Endoribonuclease activities of Trypanosoma brucei mitochondria.

作者信息

Salavati Reza, Panigrahi Aswini K, Morach Barbara A, Palazzo Setareh S, Igo Robert P, Stuart Kenneth

机构信息

Seattle Biomedical Research Institute and Department of Pathobiology, University of Washington, 4 Nickerson Street, Seattle, WA 98109, USA.

出版信息

Mol Biochem Parasitol. 2002 Mar;120(1):23-31. doi: 10.1016/s0166-6851(01)00431-5.

Abstract

RNA editing in kinetoplastids is a type of post-transcriptional processing that changes mitochondrial mRNA sequences by the addition or deletion of uridines. Multiple enzymatic activities, such as endoribonuclease and RNA ligase, are associated with this process and exist in a multienzyme complex. Endonuclease activities from Trypanosoma brucei mitochondrial extracts were fractionated by sequential ion exchange and gel filtration chromatography. The RNA editing specific endonuclease activity co-fractionated with in vitro editing while another endonuclease activity with a different substrate specificity, and the majority of mtRNase P activity fractionated away from the editing activity. The pH, salt, temperature, and Mg(2+) optima of all three endonucleases were determined. All three activities are sensitive to high temperature and protease digestion. In addition, treatment with micrococcal nuclease resulted in partial disruption of the editing complex and decreased pre-cleaved in vitro insertion editing activity, suggesting that both RNA(s) and protein(s) are necessary in the intact functional complex.

摘要

动质体中的RNA编辑是一种转录后加工类型,通过添加或删除尿苷来改变线粒体mRNA序列。多种酶活性,如核糖核酸内切酶和RNA连接酶,与该过程相关,并存在于多酶复合物中。通过连续离子交换和凝胶过滤色谱法对布氏锥虫线粒体提取物中的核酸内切酶活性进行了分级分离。RNA编辑特异性核酸内切酶活性与体外编辑共分级分离,而另一种具有不同底物特异性的核酸内切酶活性以及大部分mtRNase P活性则与编辑活性分离。测定了所有三种核酸内切酶的最适pH、盐、温度和Mg(2+)。所有三种活性都对高温和蛋白酶消化敏感。此外,用微球菌核酸酶处理导致编辑复合物部分破坏,并降低了预切割的体外插入编辑活性,这表明完整的功能复合物中RNA和蛋白质都是必需的。

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