Odaert M, Devalckenaere A, Trieu-Cuot P, Simonet M
Laboratoire de Bactériologie-Hygiène, Faculté de Médecine Henri Warembourg, Lille, France.
J Bacteriol. 1998 Jan;180(1):178-81. doi: 10.1128/JB.180.1.178-181.1998.
The genome of Yersinia pestis, the causative agent of plague, contains at least 30 copies of an element, designated IS1541, which is structurally related to IS200 (85% identity). One such element is inserted within the chromosomal inv gene (M. Simonet, B. Riot, N. Fortineau, and P. Berche, Infect. Immun. 64:375-379, 1996). We characterized other IS1541 insertions by cloning 14 different Y. pestis 6/69M loci carrying a single copy of this insertion sequence (IS) into Escherichia coli and, for each element, sequencing 250 bp of both flanking regions. In no case was this IS element inserted into large open reading frames; however, in eight cases, it was detected downstream (17 to 139 bp) of genes thought to be transcribed monocistronically or which constituted the last gene of an operon, and in only one case was it detected upstream (37 bp) of the first gene of an operon. Sequence analysis revealed stem-loop structures (deltaG, < -10 kcal) resembling rho-independent transcription terminators in 8 of the 14 insertion sites. These motifs might constitute hot spots for insertion of this IS1541 element within the Y. pestis genome.
鼠疫耶尔森菌(鼠疫的病原体)的基因组含有至少30个名为IS1541的元件拷贝,该元件在结构上与IS200相关(同一性为85%)。其中一个这样的元件插入在染色体inv基因内(M. Simonet、B. Riot、N. Fortineau和P. Berche,《感染与免疫》64:375 - 379,1996年)。我们通过将携带该插入序列(IS)单拷贝的14个不同的鼠疫耶尔森菌6/69M位点克隆到大肠杆菌中,并对每个元件两侧区域的250 bp进行测序,来表征其他IS1541插入情况。在任何情况下,这个IS元件都没有插入到大型开放阅读框中;然而,在8个案例中,它在被认为是单顺反子转录的基因下游(17至139 bp)或构成操纵子最后一个基因的下游被检测到,并且仅在一个案例中,它在操纵子第一个基因的上游(37 bp)被检测到。序列分析在14个插入位点中的8个位点揭示了类似于不依赖ρ因子的转录终止子的茎环结构(ΔG < -10 kcal)。这些基序可能构成了这个IS1541元件在鼠疫耶尔森菌基因组内插入的热点。