Vargas C, Tegos G, Drainas C, Ventosa A, Nieto J J
Department of Microbiology and Parasitology, Faculty of Pharmacy, University of Seville, Spain.
Mol Gen Genet. 1999 Jun;261(4-5):851-61. doi: 10.1007/s004380050029.
The basic replicon of the narrow-host-range plasmid pHE1 from the moderately halophilic bacterium Halomonas elongata ATCC 33174 has been identified and characterized. The replicon consists of a 1.7-kb DNA fragment, which contains the genetic information required for autonomous replication and stable maintenance. Analysis of its sequence revealed the presence of two ORFs which seem to form one transcription unit. ORF1 encodes a replication initiator protein (RepA), which has a high degree of homology to the theta-replicase (RepA) protein of ColE2 plasmid and to the RepA proteins of a family of replicons from gram-positive and gram-negative bacteria, also related to ColE2. The product encoded by ORF2 showed a certain similarity to the RepB proteins of the same family of replicons and perhaps represents the pHE1 RepB function. Deletion analysis suggests that the pHE1 origin of replication (ori) is located in an 800-bp region upstream of repA. A third putative gene, incA, was found on the complementary strand to the leader region of the repA mRNA. This, together with the presence in the 5' untranslated region of the repA mRNA of inverted repeats that could form stable stem-loop structures, suggests that the incA gene encodes a small antisense RNA. A possible control mechanism for pHE1 replication is proposed, involving an RNA molecule which sequesters the translational initiation region of the replication protein RepA. The basic replicon characterized here shows very interesting properties that should allow it to be used in the construction of cloning and expression vectors for moderate halophiles.
已鉴定并表征了中度嗜盐细菌长枝盐单胞菌ATCC 33174的窄宿主范围质粒pHE1的基本复制子。该复制子由一个1.7 kb的DNA片段组成,其中包含自主复制和稳定维持所需的遗传信息。对其序列的分析揭示了两个开放阅读框(ORF)的存在,它们似乎形成一个转录单元。ORF1编码一种复制起始蛋白(RepA),它与ColE2质粒的θ-复制酶(RepA)蛋白以及革兰氏阳性和革兰氏阴性细菌复制子家族的RepA蛋白具有高度同源性,也与ColE2相关。ORF2编码的产物与同一复制子家族的RepB蛋白有一定相似性,可能代表pHE1的RepB功能。缺失分析表明,pHE1的复制起点(ori)位于repA上游800 bp的区域。在repA mRNA前导区的互补链上发现了第三个推定基因incA。这一点,再加上repA mRNA的5'非翻译区存在可形成稳定茎环结构的反向重复序列,表明incA基因编码一种小反义RNA。提出了一种pHE1复制的可能控制机制,涉及一种隔离复制蛋白RepA翻译起始区域的RNA分子。这里表征的基本复制子显示出非常有趣的特性,这应该使其能够用于构建中度嗜盐菌的克隆和表达载体。