DiMagno L, Haselkorn R
Department of Chemistry and Molecular Genetics, University of Chicago, IL 60637.
Plant Mol Biol. 1993 Mar;21(5):835-45. doi: 10.1007/BF00027115.
Genes encoding the phycobilisome core subunits allophycocyanin alpha and beta and a small core linker protein in Synechocystis sp. strain PCC 6714 were cloned and sequenced. These genes form an operon, apcABC, with a single transcription start site and two possible termination sites, one following apcB and the other following apcC. The promoter region, like those of the apcABC operons of other cyanobacteria, does not resemble the consensus promoter sequences of Escherichia coli. However, the apcABC promoters identified in four strains of cyanobacteria have conserved sequences centered at -50 and -10 with respect to the start of transcription. The apcE gene, encoding the protein that links the phycobilisome core to the thylakoid membrane, was also cloned from Synechocystis 6714 and sequenced. It is unlinked to the apcABC operon. As in other Synechocystis strains, the LCM polypeptide encoded by the apcE gene contains three repeats of the basic phycobiliprotein linker domain. The apcE gene promoter sequence bears little resemblance to either the E. coli consensus or the apcABC promoter region, but it is similar to the corresponding regions of other cyanobacterial apcE genes. In these cases, there are conserved sequences centered at -40 and -10 with respect to the transcription start site. These conserved promoter elements from the apcABC and apcE genes were also identified in the corresponding 5'-flanking regions of eleven transcript starts for cpc genes encoding phycocyanin subunits in cyanobacteria and algal chloroplasts. These results suggest that a factor yet to be described participates in transcription of phycobiliprotein genes.
对集胞藻PCC 6714中编码藻胆体核心亚基别藻蓝蛋白α和β以及一种小核心连接蛋白的基因进行了克隆和测序。这些基因形成一个操纵子apcABC,有一个单一的转录起始位点和两个可能的终止位点,一个在apcB之后,另一个在apcC之后。其启动子区域与其他蓝细菌的apcABC操纵子的启动子区域一样,与大肠杆菌的共有启动子序列不同。然而,在四种蓝细菌菌株中鉴定出的apcABC启动子具有相对于转录起始点在-50和-10处为中心的保守序列。编码将藻胆体核心连接到类囊体膜的蛋白质的apcE基因也从集胞藻6714中克隆并测序。它与apcABC操纵子不相连。与其他集胞藻菌株一样,由apcE基因编码的LCM多肽包含基本藻胆蛋白连接域的三个重复序列。apcE基因启动子序列与大肠杆菌共有序列或apcABC启动子区域几乎没有相似之处,但与其他蓝细菌apcE基因的相应区域相似。在这些情况下,相对于转录起始点在-40和-10处为中心存在保守序列。在蓝细菌和藻类叶绿体中编码藻蓝蛋白亚基的cpc基因的11个转录起始点的相应5'侧翼区域中也鉴定出了来自apcABC和apcE基因的这些保守启动子元件。这些结果表明,一种尚未描述的因子参与藻胆蛋白基因的转录。