Zimmerly S, Guo H, Eskes R, Yang J, Perlman P S, Lambowitz A M
Department of Molecular Genetics, Ohio State University, Columbus 43210-1292, USA.
Cell. 1995 Nov 17;83(4):529-38. doi: 10.1016/0092-8674(95)90092-6.
The mobility (homing) of the yeast mitochondrial DNA group II intron al2 occurs via target DNA-primed reverse transcription at a double-strand break in the recipient DNA. Here, we show that the site-specific DNA endonuclease that makes the double-strand break is a ribonucleoprotein complex containing the al2-encoded reverse transcriptase protein and excised al2 RNA. Remarkably, the al2 RNA catalyzes cleavage of the sense strand of the recipient DNA, while the al2 protein appears to cleave the antisense strand. The RNA-catalyzed sense strand cleavage occurs via a partial reverse splicing reaction in which the protein component stabilizes the active intron structure and appears to confer preference for DNA substrates. Our results demonstrate a biologically relevant ribozyme reaction with a substrate other than RNA.
酵母线粒体DNA II类内含子al2的迁移(归巢)通过靶DNA引发的逆转录在受体DNA的双链断裂处发生。在这里,我们表明产生双链断裂的位点特异性DNA内切酶是一种核糖核蛋白复合物,包含al2编码的逆转录酶蛋白和切除的al2 RNA。值得注意的是,al2 RNA催化受体DNA有义链的切割,而al2蛋白似乎切割反义链。RNA催化的有义链切割通过部分反向剪接反应发生,其中蛋白质成分稳定活性内含子结构,并似乎赋予对DNA底物的偏好。我们的结果证明了一种与生物学相关的核酶反应,其底物不是RNA。