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广宿主范围质粒RP4上限制性内切酶识别序列的分布:分子及进化意义

Distribution of restriction enzyme recognition sequences on broad host range plasmid RP4: molecular and evolutionary implications.

作者信息

Wilkins B M, Chilley P M, Thomas A T, Pocklington M J

机构信息

Department of Genetics, University of Leicester, England.

出版信息

J Mol Biol. 1996 May 10;258(3):447-56. doi: 10.1006/jmbi.1996.0261.

Abstract

IncP alpha plasmids, exemplified by RP4, are remarkable for their broad host range. They contain strikingly few cleavage sites for many commonly used type II restriction enzymes but an overabundance of sites for certain enzymes that target G + C-rich sequences. To identify factors responsible for these distributions, the recently compiled nucleotide sequence of RP4 was analysed to determine the frequency of tetra- and hexanucleotide motifs in the 49 kb plasmid backbone. This is defined as the sectors encoding basic plasmid functions. The overabundant restriction targets in RP4 are concentrated in the backbone and contain overlapping copies of CGGC/GCCG, identified as the most abundant tetranucleotide motif in the plasmid. Motif frequencies in the RP4 backbone are shown to be similar to those in Pseudomonas aeruginosa, a natural host of RP4, with the notable exception that a number of 6-bp palindromes are underrepresented in the plasmid. It is proposed that 6-bp palindromes were counterselected as type II restriction enzyme recognition sequences. Conjugative transfer of RP4 and R751 (IncP beta) is unusually sensitive to restriction compared to enterobacterial plasmids of the IncFII and IncI1 groups, implying that IncP plasmids experienced particularly strong selection for loss of restriction targets. Pseudomonas spp. of rRNA homology group I specify many type II restriction enzymes that target 6-bp palindromes and are candidates for the evolutionary hosts of IncP alpha plasmids.

摘要

以RP4为代表的IncPα质粒以其广泛的宿主范围而著称。它们含有极少的常用II型限制酶切割位点,但针对富含G + C序列的某些酶的位点却过多。为了确定造成这些分布的因素,对最近汇编的RP4核苷酸序列进行了分析,以确定49 kb质粒骨架中四核苷酸和六核苷酸基序的频率。这被定义为编码基本质粒功能的区段。RP4中过多的限制酶切位点集中在骨架中,并包含CGGC/GCCG的重叠拷贝,这被确定为质粒中最丰富的四核苷酸基序。结果表明,RP4骨架中的基序频率与铜绿假单胞菌(RP4的天然宿主)中的基序频率相似,但值得注意的是,一些6碱基回文序列在质粒中代表性不足。有人提出,6碱基回文序列作为II型限制酶识别序列被反向选择。与IncFII和IncI1组的肠道细菌质粒相比,RP4和R751(IncPβ)的接合转移对限制异常敏感,这意味着IncP质粒在限制酶切位点缺失方面经历了特别强烈的选择。rRNA同源组I的假单胞菌属物种指定了许多靶向6碱基回文序列的II型限制酶,它们是IncPα质粒进化宿主的候选者。

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