Kalla S R, Lind L K, Lidholm J, Gustafsson P
Plant Molecular Biology Group, University of Umeå, Sweden.
J Bacteriol. 1988 Jul;170(7):2961-70. doi: 10.1128/jb.170.7.2961-2970.1988.
The phycocyanin subunit gene cluster is duplicated on the chromosome of the cyanobacterium Anacystis nidulans UTEX 625. The two gene clusters cpcB1A1 (left) and cpcB2A2 (right) are separated by about 2,500 base pairs, and in each cluster the beta-subunit gene is located upstream from the alpha-subunit gene. Filter hybridizations with phycocyanin-specific probes to total RNA detected at least two major transcripts that were 1,300 to 1,400 nucleotides long. Besides these major mRNA species, two minor transcripts of 3,400 and 3,700 nucleotides covering one of the gene clusters and the region between the clusters were found. No additional minor transcripts were found in the intergenic region between the two phycocyanin gene clusters. The lengths of the major mRNAs indicated that the beta- and alpha-subunit genes were cotranscribed. No apparent homologies were found when the DNA sequences located upstream from the proposed ribosome-binding site of the two phycocyanin beta-subunit genes were compared. Northern hybridizations with gene cluster-specific probes from the regions 5' of the beta-subunit genes, as well as S1 nuclease mapping and mRNA primer extension experiments, showed that both gene clusters were transcribed. The minor transcripts were found to initiate upstream from the left gene cluster. Two mRNA 5' ends were mapped upstream from the cpcB1A1 gene cluster, while only one 5' end was mapped in front of the cpcB2A2 gene cluster. All transcripts were present in RNA preparations from cultures grown under high levels of white light as well as under low levels of red light. The level of phycocyanin-specific mRNA, measured as part of the total RNA, was lower under low levels of red light compared with that under high levels of white light. Conserved sequence motifs were found when the promoter region of the cpcB1A1 gene cluster and promoter regions from other cyanobacterial photosynthesis genes were compared. The DNA sequences covering the proposed transcriptional attenuators and transcriptional stop signals contained several potential hairpin structures. One potential hairpin structure was located immediately downstream of the left phycocyanin gene cluster and was concluded to limit the level of transcription for the minor transcripts initiating upstream of the cpcB1A1 gene cluster.
藻蓝蛋白亚基基因簇在集胞藻625(Anacystis nidulans UTEX 625)的染色体上发生了重复。两个基因簇cpcB1A1(左侧)和cpcB2A2(右侧)被大约2500个碱基对隔开,并且在每个簇中,β亚基基因位于α亚基基因的上游。用藻蓝蛋白特异性探针与总RNA进行滤膜杂交,检测到至少两种主要转录本,长度为1300至1400个核苷酸。除了这些主要的mRNA种类外,还发现了两种较小的转录本,长度分别为3400和3700个核苷酸,覆盖其中一个基因簇以及两个簇之间的区域。在两个藻蓝蛋白基因簇之间的基因间隔区未发现其他较小的转录本。主要mRNA的长度表明β亚基基因和α亚基基因是共转录的。当比较两个藻蓝蛋白β亚基基因推测的核糖体结合位点上游的DNA序列时,未发现明显的同源性。用来自β亚基基因5'区域的基因簇特异性探针进行Northern杂交,以及S1核酸酶图谱分析和mRNA引物延伸实验表明,两个基因簇都被转录。发现较小的转录本在左侧基因簇的上游起始。在cpcB1A1基因簇上游定位了两个mRNA 5'末端,而在cpcB2A2基因簇前面只定位了一个5'末端。所有转录本都存在于在高强度白光以及低强度红光下培养的细胞的RNA制剂中。作为总RNA的一部分测量的藻蓝蛋白特异性mRNA水平,在低强度红光下比在高强度白光下低。当比较cpcB1A1基因簇的启动子区域和其他蓝藻光合作用基因的启动子区域时,发现了保守的序列基序。覆盖推测的转录衰减子和转录终止信号的DNA序列包含几个潜在的发夹结构。一个潜在的发夹结构位于左侧藻蓝蛋白基因簇的紧下游,并得出结论认为它限制了在cpcB1A1基因簇上游起始的较小转录本的转录水平。