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编码逆转录酶、成熟酶和DNA内切核酸酶活性的细菌II类内含子:成熟酶活性的生化证明以及内含子内新遗传信息的插入

A bacterial group II intron encoding reverse transcriptase, maturase, and DNA endonuclease activities: biochemical demonstration of maturase activity and insertion of new genetic information within the intron.

作者信息

Matsuura M, Saldanha R, Ma H, Wank H, Yang J, Mohr G, Cavanagh S, Dunny G M, Belfort M, Lambowitz A M

机构信息

Department of Molecular Genetics, The Ohio State University, Columbus, Ohio 43210-1292, USA.

出版信息

Genes Dev. 1997 Nov 1;11(21):2910-24. doi: 10.1101/gad.11.21.2910.

Abstract

The Lactococcus lactis group II intron Ll.ltrB is similar to mobile yeast mtDNA group II introns, which encode reverse transcriptase, RNA maturase, and DNA endonuclease activities for site-specific DNA insertion. Here, we show that the Lactococcal intron can be expressed and spliced efficiently in Escherichia coli. The intron-encoded protein LtrA has reverse transcriptase and RNA maturase activities, with the latter activity shown both in vivo and in vitro, a first for any group II intron-encoded protein. As for the yeast mtDNA introns, the DNA endonuclease activity of the Lactococcal intron is associated with RNP particles containing both the intron-encoded protein and the excised intron RNA. Also, the intron RNA cleaves the sense-strand of the recipient DNA by a reverse splicing reaction, whereas the intron-encoded protein cleaves the antisense strand. The Lactococcal intron endonuclease can be obtained in large quantities by coexpression of the LtrA protein with the intron RNA in E. coli or reconstituted in vitro by incubating the expressed LtrA protein with in vitro-synthesized intron RNA. Furthermore, the specificity of the endonuclease and reverse splicing reactions can be changed predictably by modifying the RNA component. Expression in E. coli facilitates the use of group II introns for the targeting of specific foreign sequences to a desired site in DNA.

摘要

乳酸乳球菌II组内含子Ll.ltrB与可移动的酵母线粒体DNA II组内含子相似,后者编码逆转录酶、RNA成熟酶和DNA内切核酸酶活性,用于位点特异性DNA插入。在此,我们表明乳球菌内含子可在大肠杆菌中高效表达和剪接。内含子编码的蛋白质LtrA具有逆转录酶和RNA成熟酶活性,后者的活性在体内和体外均得到证实,这在任何II组内含子编码的蛋白质中尚属首次。与酵母线粒体DNA内含子一样,乳球菌内含子的DNA内切核酸酶活性与包含内含子编码蛋白质和切除的内含子RNA的核糖核蛋白颗粒相关。此外,内含子RNA通过反向剪接反应切割受体DNA的有义链,而内含子编码的蛋白质切割反义链。通过在大肠杆菌中共表达LtrA蛋白和内含子RNA,或通过将表达的LtrA蛋白与体外合成的内含子RNA孵育在体外进行重组,可大量获得乳球菌内含子内切核酸酶。此外,通过修饰RNA成分,可以可预测地改变内切核酸酶和反向剪接反应的特异性。在大肠杆菌中的表达便于利用II组内含子将特定的外源序列靶向到DNA中的所需位点。

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