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本文引用的文献

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Evolutionary dynamics of insertion sequences in Helicobacter pylori.幽门螺杆菌中插入序列的进化动力学
J Bacteriol. 2004 Nov;186(22):7508-20. doi: 10.1128/JB.186.22.7508-7520.2004.
2
Tracing clonality of Helicobacter pylori infecting family members from analysis of DNA sequences of three housekeeping genes (ureI, atpA and ahpC), deduced amino acid sequences, and pathogenicity-associated markers (cagA and vacA).通过分析三个管家基因(ureI、atpA和ahpC)的DNA序列、推导的氨基酸序列以及致病性相关标志物(cagA和vacA)来追踪幽门螺杆菌感染家庭成员的克隆性。
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Traces of human migrations in Helicobacter pylori populations.幽门螺杆菌群体中的人类迁徙痕迹。
Science. 2003 Mar 7;299(5612):1582-5. doi: 10.1126/science.1080857.
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Identification of strain-specific genes located outside the plasticity zone in nine clinical isolates of Helicobacter pylori.幽门螺杆菌九株临床分离株中可塑性区外菌株特异性基因的鉴定。
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5
Transposable element ISHp608 of Helicobacter pylori: nonrandom geographic distribution, functional organization, and insertion specificity.幽门螺杆菌的转座元件ISHp608:非随机地理分布、功能组织及插入特异性
J Bacteriol. 2002 Feb;184(4):992-1002. doi: 10.1128/jb.184.4.992-1002.2002.
6
Recombination and mutation during long-term gastric colonization by Helicobacter pylori: estimates of clock rates, recombination size, and minimal age.幽门螺杆菌长期胃定植过程中的重组与突变:时钟速率、重组大小及最小年龄的估计
Proc Natl Acad Sci U S A. 2001 Dec 18;98(26):15056-61. doi: 10.1073/pnas.251396098. Epub 2001 Dec 11.
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Perspective: transposable elements, parasitic DNA, and genome evolution.观点:转座元件、寄生DNA与基因组进化。
Evolution. 2001 Jan;55(1):1-24. doi: 10.1111/j.0014-3820.2001.tb01268.x.
8
Helicobacter pylori: clonal population structure and restricted transmission within families revealed by molecular typing.幽门螺杆菌:分子分型揭示的克隆群体结构及家庭内有限传播
J Clin Microbiol. 2000 Oct;38(10):3646-51. doi: 10.1128/JCM.38.10.3646-3651.2000.
9
Functional organization and insertion specificity of IS607, a chimeric element of Helicobacter pylori.幽门螺杆菌嵌合元件IS607的功能组织与插入特异性
J Bacteriol. 2000 Oct;182(19):5300-8. doi: 10.1128/JB.182.19.5300-5308.2000.
10
Tissue-specific gene expression identifies a gene in the lysogenic phage Gifsy-1 that affects Salmonella enterica serovar typhimurium survival in Peyer's patches.组织特异性基因表达鉴定出溶原性噬菌体Gifsy-1中的一个基因,该基因影响鼠伤寒沙门氏菌在派尔集合淋巴结中的存活。
J Bacteriol. 2000 Aug;182(16):4406-13. doi: 10.1128/JB.182.16.4406-4413.2000.

幽门螺杆菌新型嵌合转座元件ISHp609的序列组织与插入特异性

Sequence organization and insertion specificity of the novel chimeric ISHp609 transposable element of Helicobacter pylori.

作者信息

Kersulyte Dangeruta, Kalia Awdhesh, Zhang MaoJun, Lee Hae-Kyung, Subramaniam Dharmalingam, Kiuduliene Levute, Chalkauskas Henrikas, Berg Douglas E

机构信息

Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA.

出版信息

J Bacteriol. 2004 Nov;186(22):7521-8. doi: 10.1128/JB.186.22.7521-7528.2004.

DOI:10.1128/JB.186.22.7521-7528.2004
PMID:15516563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC524915/
Abstract

Here we describe ISHp609 of Helicobacter pylori, a new member of the IS605 mobile element family that is novel and contains two genes whose functions are unknown, jhp960 and jhp961, in addition to homologs of two other H. pylori insertion sequence (IS) element genes, orfA, which encodes a putative serine recombinase-transposase, and orfB, whose homologs in other species are also often annotated as genes that encode transposases. The complete four-gene element was found in 10 to 40% of strains obtained from Africa, India, Europe, and the Americas but in only 1% of East Asian strains. Sequence comparison of 10 representative ISHp609 elements revealed higher levels of DNA sequence matches (99%) than those seen in normal chromosomal genes (88 to 98%) or in other IS elements (95 to 97% for IS605, IS606, and IS607) from the same H. pylori populations. Sequence analysis suggested that ISHp609 can insert at many genomic sites with its left end preferentially next to TAT, with no target specificity for its right end, and without duplicating or deleting target sequences. A deleted form of ISHp609, containing just jhp960 and jhp961 and 37 bp of orfA, found in reference strain J99, was at the same chromosomal site in 15 to 40% of the strains from many geographic regions but again in only 1% of the East Asian strains. The abundance and sequence homogeneity of ISHp609 and of this nonmobile remnant suggested a recent bottleneck and then rapid spread in H. pylori populations, possibly selected by the contributions of the elements to bacterial fitness.

摘要

在这里,我们描述了幽门螺杆菌的ISHp609,它是IS605可移动元件家族的一个新成员,该家族新颖独特,除了另外两个幽门螺杆菌插入序列(IS)元件基因(orfA和orfB)的同源物外,还包含两个功能未知的基因jhp960和jhp961,其中orfA编码一种假定的丝氨酸重组酶 - 转座酶,而orfB在其他物种中的同源物通常也被注释为编码转座酶的基因。在从非洲、印度、欧洲和美洲获得的菌株中,10%至40%的菌株中发现了完整的四基因元件,但在东亚菌株中仅占1%。对10个代表性ISHp609元件的序列比较显示,其DNA序列匹配水平(99%)高于同一幽门螺杆菌群体中正常染色体基因(88%至98%)或其他IS元件(IS605、IS606和IS607为95%至97%)。序列分析表明,ISHp609可以在许多基因组位点插入,其左端优先紧邻TAT,右端没有靶标特异性,并且不会复制或删除靶标序列。在参考菌株J99中发现的一种缺失形式的ISHp609,仅包含jhp960和jhp961以及37 bp的orfA,在许多地理区域的15%至40%的菌株中位于相同的染色体位点,但在东亚菌株中同样仅占1%。ISHp609和这种非移动残余物的丰度和序列同质性表明,幽门螺杆菌群体最近经历了瓶颈效应,然后迅速传播,这可能是由这些元件对细菌适应性的贡献所选择的。