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来自乳球菌θ型复制质粒pJW563的复制子的特性分析。

Characterization of the replicon from the lactococcal theta-replicating plasmid pJW563.

作者信息

Gravesen A, Josephsen J, von Wright A, Vogensen F K

机构信息

Department of Dairy and Food Science, Royal Veterinary and Agricultural University, Frederiksberg C, Denmark.

出版信息

Plasmid. 1995 Sep;34(2):105-18. doi: 10.1006/plas.1995.9996.

Abstract

The replication region of the lactococcal plasmid pJW563 was localized to a 2.3-kb EcoRI fragment. This DNA fragment was sequenced ans a 1155-bp open reading frame, repB563, encoding a putative protein RepB563 of 385 amino acids was found. An AT-rich noncoding region, repA563, was found upstream of repB563. This segment included several direct and inverted repeats. A downstream 591-bp open reading frame, ORF X, which was not necessary for replication, was putatively translationally coupled to repB563, RepB563 supplied in trans could support replication of a plasmid containing repA563 and a truncated repB563. This observation suggests that RepB563 is a trans-acting replication protein, and repA563 the cis-acting origin of replication, repA563, repB563, and the beginning of ORF X showed high homology to similar regions in a family of lactococcal theta-replicating plasmids. The repA DNA sequences and the RepB amino acid sequences of the plasmids were aligned and the consensus sequences generated. The comparison revealed highly conserved areas among this family of plasmids. In addition, variable domains emerged, presumably having a plasmid specific function, pVS40 and pC1305 were plasmids with replication proteins showing high homology to RepB563. Despite this homology, replication from repA563 could not be supported by the pVS40 or pC1305 replication protein supplied in trans. Likewise the pJW563 protein could not support replication from the pVS40 origin. pJW563 was found to be compatible with the pVS40 and pC1305 replicons. The results indicate that pJW563 belongs to the widespread family of lactococcal theta-replicating pladmids. Despite the high homology between their replicons, the interaction between the replication origin and the protein is highly specific in many cases rendering the plasmids compatible.

摘要

乳球菌质粒pJW563的复制区域定位于一个2.3kb的EcoRI片段。对该DNA片段进行测序后,发现了一个1155bp的开放阅读框repB563,它编码一个由385个氨基酸组成的假定蛋白RepB563。在repB563的上游发现了一个富含AT的非编码区域repA563。该片段包含几个正向和反向重复序列。一个下游591bp的开放阅读框ORF X对复制不是必需的,推测它与repB563存在翻译偶联,反式提供的RepB563能够支持含有repA563和截短的repB563的质粒的复制。这一观察结果表明RepB563是一种反式作用的复制蛋白,而repA563是顺式作用的复制起点,repA563、repB563以及ORF X的起始部分与乳球菌θ型复制质粒家族中的相似区域具有高度同源性。对这些质粒的repA DNA序列和RepB氨基酸序列进行比对并生成共有序列。比较结果揭示了该质粒家族中高度保守的区域。此外,还出现了可变结构域,推测具有质粒特异性功能,pVS40和pC1305是其复制蛋白与RepB563具有高度同源性的质粒。尽管存在这种同源性,但反式提供的pVS40或pC1305复制蛋白不能支持从repA563进行复制。同样,pJW563蛋白也不能支持从pVS40起点进行复制。发现pJW563与pVS40和pC1305复制子兼容。结果表明pJW563属于广泛存在的乳球菌θ型复制质粒家族。尽管它们的复制子之间具有高度同源性,但在许多情况下,复制起点与蛋白之间的相互作用具有高度特异性,使得这些质粒相互兼容。

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