Thomm M, Sherf B A, Reeve J N
Lehrstuhl für Mikrobiologie, Universität Regensburg, Federal Republic of Germany.
J Bacteriol. 1988 Apr;170(4):1958-61. doi: 10.1128/jb.170.4.1958-1961.1988.
RNA polymerase, purified from Methanococcus vannielii, was shown by exonuclease III footprinting to bind to a 49-base-pair (bp) region of DNA in the intergenic region upstream of mcrB. S1 nuclease protection experiments demonstrated that transcription initiation in vivo occurs within this region at 32 or 33 bp 5' to the ATG translation initiation codon of mcrB and 19 or 20 bp 3' to a TATA box.
从万氏甲烷球菌中纯化出的RNA聚合酶,经核酸外切酶III足迹法显示,它能与mcrB上游基因间区域一段49个碱基对(bp)的DNA区域结合。S1核酸酶保护实验表明,体内转录起始发生在该区域内,位于mcrB的ATG翻译起始密码子5'端32或33 bp处,以及TATA框3'端19或20 bp处。