布鲁氏菌插入序列IS6501的鉴定与序列分析:基因组结构与IS6501拷贝数的关系

S Ouahrani, S Michaux, J Sri Widada, G Bourg, R Tournebize, M Ramuz, J P Liautard
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引用次数: 97

摘要

分离得到了一个名为IS6501的布鲁氏菌插入序列元件,并测定了其完整的核苷酸序列。IS6501全长836bp,在B. ovis基因组中出现20-35次,在其他布鲁氏菌基因组中出现5-15次。对插入位点的连接分析显示,4个碱基的小目标位点重复和17 bp的反向重复,其中1个不匹配。IS6501与农杆菌中鉴定的IS427具有显著的相似性(53.4%),表明它们具有共同的祖先序列。鉴定出708 bp的长ORF编码一个预计分子质量为26 kDa的蛋白,该蛋白与假定的A. tummefaciens蛋白1和结核分枝杆菌转座酶具有相同的序列。IS6501存在于我们测试的所有布鲁氏菌菌株中。采用脉冲场凝胶电泳(PFGE)对xbai -酶切DNA进行检测,或以IS6501为探针对ecori -酶切DNA进行杂交,研究了两种参考菌株(B. melitensis和B. ovis)的限制性内切片段长度多态性。白蚁3号生物品种的基因组每个基因组包含约10个IS拷贝,同一物种的田间菌株无论是用IS杂交还是用XbaI (PFGE)限制性模式都无法区分。相比之下,B. ovis基因组中的IS拷贝数在30左右,两种方法都可以区分不同的田间菌株。(摘要删节250字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification and sequence analysis of IS6501, an insertion sequence in Brucella spp.: relationship between genomic structure and the number of IS6501 copies.

An insertion sequence (IS) element of Brucella ovis, named IS6501, was isolated and its complete nucleotide sequence determined. IS6501 is 836 bp in length and occurs 20-35 times in the B. ovis genome and 5-15 times in other Brucella species. Analysis of the junctions at the sites of insertion revealed a small target site duplication of four bases and inverted repeats of 17 bp with one mismatch. IS6501 presents significant similarity (53.4%) with IS427 identified in Agrobacterium tumefaciens, suggesting a common ancestral sequence. A long ORF of 708 bp was identified encoding a protein with a predicted molecular mass of 26 kDa and sharing sequence identity with the hypothetical protein 1 of A. tumefaciens and with the transposase of Mycobacterium tuberculosis. IS6501 is present in all Brucella strains we have tested. Restriction fragment length polymorphism of reference and field strains of two species (B. melitensis and B. ovis) was studied using either pulsed field gel electrophoresis (PFGE) on XbaI-digested DNA or hybridization of EcoRI-digested DNA using IS6501 as a probe. The genome of B. melitensis biovar 3 contains about 10 IS copies per genome and field strains of the same species could not be distinguished either by IS hybridization or by XbaI (PFGE) restriction patterns. In contrast, the number of IS copies in the B. ovis genome is around 30 and the different field strains can be differentiated by both methods.(ABSTRACT TRUNCATED AT 250 WORDS)

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