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Characterization of a CACAG pentanucleotide repeat in Pasteurella haemolytica and its possible role in modulation of a novel type III restriction-modification system.

机译:溶血巴斯德氏菌中CACAG五核苷酸重复序列的表征及其在新型III型限制性修饰系统中的调控作用。

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摘要

In a previous study, a recombinant plasmid that contains a CACAG pentanucleotide repeat was isolated from a Pasteurella haemolytica A1 library. Southern hybridization analysis using a (CACAG)5probe indicated the presence of two loci that contain the pentanucleotide repeats on the genome of P.haemolytica A1. Additional hybridization analyses against genomic DNA from related microorganisms indicated that the repeats are only present in P.haemolytica and Pasteurella trehalosi T3. The various serotypes of P.haemolytica werefound to have either one or two of the CACAG repeat-containing loci. Examination of the locus designated Rpt2 by PCR and sequence analysis indicated that the number of CACAG repeats could change upon serial subculture which most likely occurs as a result of DNA slipped-strand mispairing. A plasmid carrying the Rpt2 locus was isolated and characterized. Sequenceanalysis indicated that the CACAG repeats are contained within the 5'-end of a gene that showed homology to mod genes of type III restriction-modification systems. A second open reading frame downstream was identified which showed homology to res genes of type III restriction-modification systems. Both the modification and restriction proteins could be expressed and polypeptides of the expected sizes were detected by SDS-PAGE. Restriction activity could also be detected in crude cytoplasmic extracts of Escherichia coli strains carrying the mod and res genes on recombinant plasmids.
机译:在先前的研究中,从溶血巴斯德氏菌A1文库中分离了包含CACAG五核苷酸重复序列的重组质粒。使用(CACAG)5探针进行的Southern杂交分析表明,在溶血毕赤酵母A1基因组中存在两个含有五核苷酸重复序列的基因座。针对来自相关微生物的基因组DNA的其他杂交分析表明,重复序列仅存在于溶血毕赤酵母和海藻巴斯德氏菌T3中。发现溶血假单胞菌的各种血清型具有一个或两个含有CACAG重复序列的基因座。通过PCR和序列分析对命名为Rpt2的基因座的检查表明,在连续继代培养后,CACAG重复序列的数目可能改变,这很可能是由于DNA滑链错配造成的。分离并鉴定了携带Rpt2基因座的质粒。序列分析表明,CACAG重复序列包含在一个基因的5'端,该基因与III型限制性修饰系统的mod基因具有同源性。鉴定出下游的第二个开放阅读框,其显示与III型限制性修饰系统的res基因同源。修饰蛋白和限制蛋白均可表达,并通过SDS-PAGE检测到预期大小的多肽。还可以在重组质粒上携带mod和res基因的大肠杆菌菌株的粗胞质提取物中检测到限制性活性。

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    Ryan, K A; Lo, R Y;

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  • 年度 1999
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