Amiott Elizabeth A, Jaehning Judith A
Department of Biochemistry, University of Utah, Salt Lake City, USA.
Methods Mol Biol. 2007;372:193-206. doi: 10.1007/978-1-59745-365-3_14.
Understanding the details of how genetic information is expressed from the separate mitochondrial genome requires a detailed description of the properties of the mitochondrial RNA polymerase. This nuclear-encoded enzyme is necessary and sufficient for the transcription of all mitochondrially encoded genes. Mitochondria from yeast to humans use a single-polypeptide catalytic RNA polymerase related to enzymes from bacteriophage. They also require separable transcription factors necessary for initiation at promoter sequences on the mitochondrial DNA template. It has recently become possible to work with highly purified, recombinant forms of the mitochondrial RNA polymerase subunits from yeast. This chapter describes detailed protocols for working in vitro with this purified enzyme in transcription reactions. These assays are critical for elucidating the nature of a mitochondrial promoter and for understanding how the mitochondrial RNA polymerase recognizes these DNA sequences and selectively initiates the transcription cycle, resulting in discrete transcripts.
要了解遗传信息如何从独立的线粒体基因组中表达出来的细节,需要详细描述线粒体RNA聚合酶的特性。这种由核编码的酶对于所有线粒体编码基因的转录是必需且充分的。从酵母到人类的线粒体都使用一种与噬菌体酶相关的单多肽催化RNA聚合酶。它们还需要可分离的转录因子,这些转录因子对于在线粒体DNA模板上的启动子序列处起始转录是必需的。最近,已经能够使用来自酵母的高度纯化的重组形式的线粒体RNA聚合酶亚基进行研究。本章描述了在体外转录反应中使用这种纯化酶的详细实验方案。这些测定对于阐明线粒体启动子的性质以及理解线粒体RNA聚合酶如何识别这些DNA序列并选择性地启动转录循环从而产生离散转录本至关重要。