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从豌豆根瘤菌蚕豆生物变种中分离得到的插入序列元件ISR12的特性、分布及定位

Characterization, distribution, and localization of ISRl2, and insertion sequence element isolated from Rhizobium leguminosarum bv. viciae.

作者信息

Mazurier S I, Rigottier-Gois L, Amarger N

机构信息

Institut National de la Recherche Agronomique, Laboratoire de Microbiologie des Sols, Dijon, France.

出版信息

Appl Environ Microbiol. 1996 Feb;62(2):685-93. doi: 10.1128/aem.62.2.685-693.1996.

Abstract

An insertion sequence (IS) element, ISR12, from Rhizobium leguminosarum bv. viciae strain MSDJ4184 was isolated by insertional inactivation of the sacRB gene of pSUP104-sac, which allows positive selection. ISRl2 is 932 bp long, is flanked by 17-bp imperfect terminal inverted repeats, and generated a 3-bp target site duplication. ISRl2 was found to be 63 to 77% homologous to insertion elements of the IS5 group of the IS4 superfamily. A probe incorporating a full-length copy of ISRl2 was used to screen genomic DNAs from a collection of strains and from two field populations of R. leguminosarum to detect and estimate the copy numbers of homologous sequences. Among the collection of 63 strains representing the different species and genera of members of the family Rhizobiaceae, homology to ISRl2 was found within strains belonging to Sinorhizobium meliloti and S. fredii; within four of the six recognized Rhizobium species. R. leguminosarum, R. tropici, R. etli, and R. galegae; and within Rhizobium sp. (Phaseolus) genomic species 2. The apparent copy numbers of ISRl2 varied from one to eight. Among 139 isolates of R. leguminosarum from two field populations, homology to ISRl2 was detected in 91% of the isolates from one site and in 17% from the other. Analysis of the 95 isolates that hybridize to ISRl2 revealed a total of 20 distinct hybridization patterns composed of one to three bands. Probing blots of Eckhardt gels showed that sequences with homology to ISRl2 may be found on plasmids or the chromosome. Analysis of their genomic distribution demonstrated relationships and diversity among the R. leguminosarum isolates tested.

摘要

通过对携带允许阳性选择的pSUP104 - sac的sacRB基因进行插入失活,从豌豆根瘤菌蚕豆生物型菌株MSDJ4184中分离出一个插入序列(IS)元件ISR12。ISR12长932 bp,两侧是17 bp的不完全末端反向重复序列,并产生了一个3 bp的靶位点重复。发现ISR12与IS4超家族IS5组的插入元件具有63%至77%的同源性。使用包含ISR12全长拷贝的探针,对一系列菌株以及豌豆根瘤菌的两个田间种群的基因组DNA进行筛选,以检测和估计同源序列的拷贝数。在代表根瘤菌科不同属和种的63个菌株中,在苜蓿中华根瘤菌和费氏中华根瘤菌的菌株内;在六个已确认的根瘤菌物种中的四个物种,即豌豆根瘤菌、热带根瘤菌、埃氏根瘤菌和山羊豆根瘤菌内;以及在根瘤菌属(菜豆)基因组种2内,发现了与ISR12的同源性。ISR12的表观拷贝数从1到8不等。在来自两个田间种群的139株豌豆根瘤菌分离物中,在一个位点的91%的分离物和另一个位点的17%的分离物中检测到与ISR12的同源性。对与ISR12杂交的95个分离物的分析揭示了总共20种由一到三条带组成的不同杂交模式。对埃克哈特凝胶印迹的检测表明,与ISR12具有同源性的序列可能存在于质粒或染色体上。对它们基因组分布的分析表明了所测试的豌豆根瘤菌分离物之间的关系和多样性。

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Appl Environ Microbiol. 1988 Feb;54(2):574-6. doi: 10.1128/aem.54.2.574-576.1988.
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