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1
Molecular evidence for independent occurrence of IS6110 insertions at the same sites of the genome of Mycobacterium tuberculosis in different clinical isolates.不同临床分离株中结核分枝杆菌基因组相同位点独立发生IS6110插入的分子证据。
J Bacteriol. 2001 Sep;183(18):5279-84. doi: 10.1128/JB.183.18.5279-5284.2001.
2
A Mycobacterium tuberculosis IS6110 preferential locus (ipl) for insertion into the genome.一种结核分枝杆菌IS6110插入基因组的优先位点(ipl)。
J Clin Microbiol. 1997 Feb;35(2):479-81. doi: 10.1128/jcm.35.2.479-481.1997.
3
Differences in the prevalence of IS6110 insertion sites in Mycobacterium tuberculosis strains: low and high copy number of IS6110.结核分枝杆菌菌株中IS6110插入位点流行率的差异:IS6110的低拷贝数和高拷贝数
Tuber Lung Dis. 1997;78(2):109-16. doi: 10.1016/s0962-8479(98)80003-8.
4
Mapping of IS6110 insertion sites in two epidemic strains of Mycobacterium tuberculosis.结核分枝杆菌两个流行菌株中IS6110插入位点的定位
J Clin Microbiol. 2000 Aug;38(8):2923-8. doi: 10.1128/JCM.38.8.2923-2928.2000.
5
Identification and evolution of an IS6110 low-copy-number Mycobacterium tuberculosis cluster.IS6110低拷贝数结核分枝杆菌簇的鉴定与进化
J Infect Dis. 2002 Mar 1;185(5):641-9. doi: 10.1086/339345. Epub 2002 Feb 14.
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Analysis of the regions responsible for IS6110 RFLP in a single Mycobacterium tuberculosis strain.单一结核分枝杆菌菌株中负责IS6110限制性片段长度多态性区域的分析。
Res Microbiol. 1992 Oct;143(8):767-72. doi: 10.1016/0923-2508(92)90104-v.
7
Use of spoligotyping to study the evolution of the direct repeat locus by IS6110 transposition in Mycobacterium tuberculosis.利用间隔寡核苷酸分型技术研究结核分枝杆菌中IS6110转座导致的直接重复序列位点的进化。
J Clin Microbiol. 2001 Apr;39(4):1595-9. doi: 10.1128/JCM.39.4.1595-1599.2001.
8
Combined use of Amplified Fragment Length Polymorphism and IS6110-RFLP in fingerprinting clinical isolates of Mycobacterium tuberculosis from Kerala, South India.扩增片段长度多态性与IS6110-限制性片段长度多态性联合用于印度南部喀拉拉邦结核分枝杆菌临床分离株的指纹图谱分析
BMC Infect Dis. 2007 Jul 28;7:86. doi: 10.1186/1471-2334-7-86.
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Evolution of the IS6110-based restriction fragment length polymorphism pattern during the transmission of Mycobacterium tuberculosis.结核分枝杆菌传播过程中基于IS6110的限制性片段长度多态性模式的演变
J Clin Microbiol. 2002 Apr;40(4):1277-82. doi: 10.1128/JCM.40.4.1277-1282.2002.
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IS6110 transposition and evolutionary scenario of the direct repeat locus in a group of closely related Mycobacterium tuberculosis strains.一组密切相关的结核分枝杆菌菌株中IS6110转座及直接重复序列位点的进化情况
J Bacteriol. 1998 Apr;180(8):2102-9. doi: 10.1128/JB.180.8.2102-2109.1998.

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Transposition mechanism, molecular characterization and evolution of IS6110, the specific evolutionary marker of Mycobacterium tuberculosis complex.结核分枝杆菌复合群的特异性进化标记IS6110的转座机制、分子特征及进化
Mol Biol Rep. 2017 Feb;44(1):25-34. doi: 10.1007/s11033-016-4084-x. Epub 2016 Oct 20.
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Mapping IS6110 in high-copy number Mycobacterium tuberculosis strains shows specific insertion points in the Beijing genotype.高拷贝数结核分枝杆菌菌株中 IS6110 的图谱显示,北京基因型有特定的插入点。
BMC Genomics. 2013 Jun 25;14:422. doi: 10.1186/1471-2164-14-422.
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Independent large scale duplications in multiple M. tuberculosis lineages overlapping the same genomic region.多个结核分枝杆菌谱系中独立的大片段重复,重叠相同的基因组区域。
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Polymorphic exact tandem repeat A (PETRA): a newly defined lineage of mycobacterium tuberculosis in israel originating predominantly in Sub-Saharan Africa.多态性精确串联重复 A(PETRA):以色列新定义的分枝杆菌结核分支,主要起源于撒哈拉以南非洲。
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7
Molecular typing of Mycobacterium tuberculosis by using nine novel variable-number tandem repeats across the Beijing family and low-copy-number IS6110 isolates.利用跨越北京家族和低拷贝数IS6110分离株的九个新型可变数目串联重复序列对结核分枝杆菌进行分子分型。
J Clin Microbiol. 2003 Sep;41(9):4224-30. doi: 10.1128/JCM.41.9.4224-4230.2003.
8
PCR-based methodology for detecting multidrug-resistant strains of Mycobacterium tuberculosis Beijing family circulating in Russia.用于检测在俄罗斯传播的结核分枝杆菌北京家族多重耐药菌株的基于聚合酶链反应的方法。
Eur J Clin Microbiol Infect Dis. 2003 Jun;22(6):342-8. doi: 10.1007/s10096-003-0944-0. Epub 2003 Jun 3.
9
Evolutionary relationships among strains of Mycobacterium tuberculosis with few copies of IS6110.具有少量IS6110拷贝的结核分枝杆菌菌株之间的进化关系。
J Bacteriol. 2003 Apr;185(8):2555-62. doi: 10.1128/JB.185.8.2555-2562.2003.
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Determining the genomic locations of repetitive DNA sequences with a whole-genome microarray: IS6110 in Mycobacterium tuberculosis.利用全基因组微阵列确定重复DNA序列的基因组位置:结核分枝杆菌中的IS6110
J Clin Microbiol. 2002 Jun;40(6):2192-8. doi: 10.1128/JCM.40.6.2192-2198.2002.

本文引用的文献

1
Disruption of coding regions by IS6110 insertion in Mycobacterium tuberculosis.结核分枝杆菌中IS6110插入对编码区的破坏
Tuber Lung Dis. 1999;79(6):349-59. doi: 10.1054/tuld.1999.0218.
2
Characterization of the phylogenetic distribution and chromosomal insertion sites of five IS6110 elements in Mycobacterium tuberculosis: non-random integration in the dnaA-dnaN region.结核分枝杆菌中五个IS6110元件的系统发育分布和染色体插入位点的特征:在dnaA-dnaN区域的非随机整合
Tuber Lung Dis. 1998;79(1):31-42. doi: 10.1054/tuld.1998.0003.
3
Characterization of IS1547, a new member of the IS900 family in the Mycobacterium tuberculosis complex, and its association with IS6110.结核分枝杆菌复合群中IS900家族新成员IS1547的特性及其与IS6110的关联
J Bacteriol. 1999 Feb;181(3):1021-4. doi: 10.1128/JB.181.3.1021-1024.1999.
4
IS6110-mediated deletions of wild-type chromosomes of Mycobacterium tuberculosis.IS6110介导的结核分枝杆菌野生型染色体缺失
J Bacteriol. 1999 Feb;181(3):1014-20. doi: 10.1128/JB.181.3.1014-1020.1999.
5
Nonrandom association of IS6110 and Mycobacterium tuberculosis: implications for molecular epidemiological studies.IS6110与结核分枝杆菌的非随机关联:对分子流行病学研究的启示
J Clin Microbiol. 1998 May;36(5):1410-3. doi: 10.1128/JCM.36.5.1410-1413.1998.
6
IS6110 transposition and evolutionary scenario of the direct repeat locus in a group of closely related Mycobacterium tuberculosis strains.一组密切相关的结核分枝杆菌菌株中IS6110转座及直接重复序列位点的进化情况
J Bacteriol. 1998 Apr;180(8):2102-9. doi: 10.1128/JB.180.8.2102-2109.1998.
7
Restriction fragment length polymorphism study of Mycobacterium tuberculosis in Thailand using IS6110 as probe.以IS6110为探针的泰国结核分枝杆菌限制性片段长度多态性研究
Int J Tuberc Lung Dis. 1997 Aug;1(4):370-6.
8
Restricted structural gene polymorphism in the Mycobacterium tuberculosis complex indicates evolutionarily recent global dissemination.结核分枝杆菌复合群中受限的结构基因多态性表明其在全球范围内的传播是近期进化的结果。
Proc Natl Acad Sci U S A. 1997 Sep 2;94(18):9869-74. doi: 10.1073/pnas.94.18.9869.
9
Target site selection in transposition.转座中的靶位点选择
Annu Rev Biochem. 1997;66:437-74. doi: 10.1146/annurev.biochem.66.1.437.
10
Nonrandom location of IS1 elements in the genomes of natural isolates of Escherichia coli.大肠杆菌自然分离株基因组中IS1元件的非随机定位。
Mol Biol Evol. 1997 Jul;14(7):725-32. doi: 10.1093/oxfordjournals.molbev.a025812.

不同临床分离株中结核分枝杆菌基因组相同位点独立发生IS6110插入的分子证据。

Molecular evidence for independent occurrence of IS6110 insertions at the same sites of the genome of Mycobacterium tuberculosis in different clinical isolates.

作者信息

Fang Z, Kenna D T, Doig C, Smittipat D N, Palittapongarnpim P, Watt B, Forbes K J

机构信息

Public Health Laboratory Services Mycobacteria Reference Unit and Department of Infection, Guy's, King's and St. Thomas' School of Medicine, London, United Kingdom.

出版信息

J Bacteriol. 2001 Sep;183(18):5279-84. doi: 10.1128/JB.183.18.5279-5284.2001.

DOI:10.1128/JB.183.18.5279-5284.2001
PMID:11514510
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC95409/
Abstract

Several characteristics of Mycobacterium tuberculosis (e.g., conserved genome and low growth rate) have severely restricted the study of the microorganism. The discovery of IS6110 raised hopes of overcoming these obstacles. However, our knowledge of this IS element is relatively limited; even its two basic characteristics (transposition mechanism and target site selection) are far from well understood. In this study, IS6110 insertions in ipl loci (iplA and iplB) in two collections of clinical isolates of M. tuberculosis from different geographic locations, one from Scotland and the other from Thailand, were investigated. Five different IS6110 insertions in the loci were identified: ipl-4::IS6110, ipl-5::IS6110, ipl-11::IS6110, ipl-12::IS6110, and ipl-13::IS6110. An attempt to establish the phylogenetic relationship of the isolates containing these insertions was unsuccessful, suggesting that some of these insertions may have arisen from more than one event. This possibility is further supported by the observation that IS6110 copies existed in the same site but with different orientations in different isolates, and the insertion site of ipl-1::IS6110 harbored IS6110 copies in both iplA and iplB in different strains. All these suggest the independent occurrence of IS6110 insertions at the same sites of the genome of M. tuberculosis in different clinical isolates. The implications of this finding are discussed.

摘要

结核分枝杆菌的几个特性(如基因组保守和生长速度缓慢)严重限制了对该微生物的研究。IS6110的发现为克服这些障碍带来了希望。然而,我们对这个插入序列元件的了解相对有限;甚至其两个基本特性(转座机制和靶位点选择)也远未被充分理解。在本研究中,调查了来自不同地理位置的两批结核分枝杆菌临床分离株(一批来自苏格兰,另一批来自泰国)中ipl基因座(iplA和iplB)的IS6110插入情况。在这些基因座中鉴定出了五种不同的IS6110插入:ipl - 4::IS6110、ipl - 5::IS6110、ipl - 11::IS6110、ipl - 12::IS6110和ipl - 13::IS6110。尝试建立含有这些插入的分离株的系统发育关系未成功,这表明其中一些插入可能源于不止一次事件。同一位置的IS6110拷贝在不同分离株中方向不同,以及ipl - 1::IS6110的插入位点在不同菌株的iplA和iplB中都含有IS6110拷贝,这些观察结果进一步支持了这种可能性。所有这些都表明IS6110在不同临床分离株的结核分枝杆菌基因组相同位点独立发生插入。本文讨论了这一发现的意义。