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Identification of the minimal replicon and the origin of replication of the crenarchaeal plasmid pRN1

机译:crenarchaeal质粒pRN1的最小复制子和复制起点的鉴定

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摘要

AbstractWe have determined the minimal replicon of the crenarchaeal plasmid pRN1. It consists of 3097 base pairs amounting to 58% of the genome of pRN1. The minimal replicon comprises replication operon orf56/orf904 coding for a transcriptional repressor and the replication protein of pRN1. An upstream region of 64 bp that contains the promoter of the replication operon is essential as well as 166 bp of sequence downstream of the orf904 gene. This region contains a putative transcriptional terminator and a 100 nucleotides long stem–loop structure. Only the latter structure was shown to be required for replication. In addition replication was sustained when the stem–loop was displaced to another part of the pRN1 sequence. By mutational analysis we also find that the integrity of the stem–loop structure is required to maintain the replication of pRN1-derived constructs. As similar stem–loop structures are also present in other members of the pRN family, we suggest that this conserved structural element could be the origin of replication for the pRN plasmids. Further bioinformatic analysis revealed that the domain structure of the replication protein and the presence of a similar stem–loop structure as the putative replication origin are also found in several bacteriophages.
机译:摘要我们已经确定了crenarchaeal质粒pRN1的最小复制子。它由3097个碱基对组成,占pRN1基因组的58%。最小复制子包含编码转录阻遏子和pRN1复制蛋白的复制操纵子orf56 / orf904。包含复制操纵子启动子的64 bp上游区域以及orf904基因下游166 bp序列都是必不可少的。该区域包含一个推定的转录终止子和一个100个核苷酸长的茎-环结构。仅显示后一种结构是复制所必需的。此外,当茎环转移到pRN1序列的另一部分时,复制得以维持。通过突变分析,我们还发现茎环结构的完整性是维持pRN1衍生结构复制所必需的。由于在pRN家族的其他成员中也存在类似的茎-环结构,因此我们建议这种保守的结构元件可能是pRN质粒复制的起点。进一步的生物信息学分析表明,在几种噬菌体中也发现了复制蛋白的结构域结构和与假定的复制起点相似的茎-环结构。

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