Hanic-Joyce P J, Gray M W
Department of Biochemistry, Dalhousie University, Halifax, Nova Scotia, Canada.
Mol Cell Biol. 1991 Apr;11(4):2035-9. doi: 10.1128/mcb.11.4.2035-2039.1991.
To investigate transcriptional mechanisms in plant mitochondria, we have developed an accurate and efficient in vitro transcription system consisting of a partially purified wheat mitochondrial extract programmed with cloned DNA templates containing the promoter for the wheat mitochondrial cytochrome oxidase subunit II gene (coxII). Using this system, we localize the coxII promoter to a 372-bp region spanning positions -56 to -427 relative to the coxII translation initiation codon. We show that in vitro transcription of coxII is initiated at position -170, precisely the same site at which transcription is initiated in vivo. Transcription begins within the sequence GTATAGTAAGTA (the initiating nucleotide is underlined), which is similar to the consensus yeast mitochondrial promoter motif, (A/T)TATAAGTA. This is the first in vitro system that faithfully reproduces in vivo transcription of a plant mitochondrial gene.
为了研究植物线粒体中的转录机制,我们开发了一种准确高效的体外转录系统,该系统由部分纯化的小麦线粒体提取物组成,并以含有小麦线粒体细胞色素氧化酶亚基II基因(coxII)启动子的克隆DNA模板进行编程。利用该系统,我们将coxII启动子定位到一个372 bp的区域,该区域相对于coxII翻译起始密码子跨越-56至-427位。我们表明,coxII的体外转录起始于-170位,这与体内转录起始的位点完全相同。转录在序列GTATAGTAAGTA(起始核苷酸下划线)内开始,该序列类似于酵母线粒体启动子共有基序(A/T)TATAAGTA。这是第一个忠实地再现植物线粒体基因体内转录的体外系统。