Brown J W, Thomm M, Beckler G S, Frey G, Stetter K O, Reeve J N
Molecular, Cellular and Developmental Biology Program, Ohio State University, Columbus 43210.
Nucleic Acids Res. 1988 Jan 11;16(1):135-50. doi: 10.1093/nar/16.1.135.
Transcription initiation of the hisA gene in vivo in the archaebacterium Methanococcus vannielii, as determined by nuclease S1 and primer extension analyses, occurs 73 base pairs (bp) upstream of the translation initiation site. Binding of M. vannielii RNA polymerase protects 43 bp of DNA, from 35 bp upstream (-35) to 8 bp downstream (+8) of the hisA mRNA initiation site, from digestion by DNase I and exonuclease III. An A + T rich region, with a sequence which conforms to the consensus sequence for promoters of stable RNA-encoding genes in methanogens, is found at the same location (-25) upstream of the polypeptide-encoding hisA gene. It appears therefore that a TATA-like sequence is also an element of promoters which direct transcription of polypeptide-encoding genes in this archaebacterium.
通过核酸酶S1和引物延伸分析确定,在古细菌万氏甲烷球菌体内,组氨酸A(hisA)基因的转录起始发生在翻译起始位点上游73个碱基对(bp)处。万氏甲烷球菌RNA聚合酶的结合可保护43 bp的DNA不被DNase I和核酸外切酶III消化,这段DNA从hisA mRNA起始位点上游35 bp(-35)到下游8 bp(+8)。在编码多肽的hisA基因上游相同位置(-25)发现了一个富含A+T的区域,其序列与产甲烷菌中稳定RNA编码基因启动子的共有序列一致。因此,类似TATA的序列似乎也是指导这种古细菌中多肽编码基因转录的启动子元件。