Finch P W, Wilson R E, Brown K, Hickson I D, Tomkinson A E, Emmerson P T
Nucleic Acids Res. 1986 Jun 11;14(11):4437-51. doi: 10.1093/nar/14.11.4437.
The nucleotide sequence of a 6,000 bp region of the E. coli chromosome that includes the 3' end of the coding region for the thyA gene and the entire recC gene has been determined. The proposed coding region for the RecC protein is 3369 nucleotides long, which would encode a polypeptide consisting of 1122 amino acids with a calculated molecular mass of 129 kDa. Mung bean nuclease mapping of a recC specific transcript produced in vivo indicates that transcription of recC is initiated 80 bp upstream of the translational start point. A weak promoter sequence situated 5' to the transcription initiation point has been identified. In the 1953 bp thyA-recC intergenic region there are three open reading frames that would code for polypeptides of molecular mass 30 kDa, 13.5 kDa and 12 kDa, respectively. Although the first and third of these open reading frames are preceded by possible ribosome binding sites, no obvious promoter sequences could be identified. Moreover, transcripts for these reading frames could not be detected.
已确定大肠杆菌染色体一个6000 bp区域的核苷酸序列,该区域包括thyA基因编码区的3'端和整个recC基因。RecC蛋白的推测编码区长3369个核苷酸,将编码一个由1122个氨基酸组成的多肽,计算分子量为129 kDa。对体内产生的recC特异性转录本进行绿豆核酸酶图谱分析表明,recC的转录起始于翻译起始点上游80 bp处。已鉴定出位于转录起始点5'端的一个弱启动子序列。在1953 bp的thyA-recC基因间隔区有三个开放阅读框,分别编码分子量为30 kDa、13.5 kDa和12 kDa的多肽。尽管这些开放阅读框中的第一个和第三个之前可能有核糖体结合位点,但未鉴定出明显的启动子序列。此外,未检测到这些阅读框的转录本。