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耻垢分枝杆菌的IS1549在插入时会形成长的直接重复序列。

IS1549 from Mycobacterium smegmatis forms long direct repeats upon insertion.

作者信息

Plikaytis B B, Crawford J T, Shinnick T M

机构信息

Division of AIDS, STD, and TB Laboratory Research, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA.

出版信息

J Bacteriol. 1998 Mar;180(5):1037-43. doi: 10.1128/JB.180.5.1037-1043.1998.

DOI:10.1128/JB.180.5.1037-1043.1998
PMID:9495740
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC106989/
Abstract

A new insertion element, IS1549, was identified serendipitously from Mycobacterium smegmatis LR222 during experiments using a vector designed to detect the excision of IS6110 from between the promoter region and open reading frame (ORF) of an aminoglycoside phosphotransferase gene. Six of the kanamycin-resistant isolates had a previously unidentified insertion element upstream of the ORF of the aph gene. The 1,634-bp sequence contained a single ORF of 504 amino acids with 85% G+C content in the third codon position. The putative protein sequence showed a distant relationship to the transposase of IS231, which is a member of the IS4 family of insertion elements. IS1549 contains 11-bp terminal inverted repeats and is characterized by the formation of unusually long and variable-length (71- to 246-bp) direct repeats of the target DNA during transposition. Southern blot analysis revealed that five copies of IS1549 are present in LR222, but not all M. smegmatis strains carry this element. Only strains with a 65-kDa antigen gene with a PCR-restriction fragment length polymorphism type identical to that of M. smegmatis 607 contain IS1549. None of 13 other species of Mycobacterium tested by PCR with two sets of primers specific for IS1549 were positive for the expected amplified product.

摘要

在使用一种旨在检测氨基糖苷磷酸转移酶基因启动子区域与开放阅读框(ORF)之间IS6110切除情况的载体进行实验过程中,偶然从耻垢分枝杆菌LR222中鉴定出一种新的插入元件IS1549。六株卡那霉素抗性分离株在aph基因的ORF上游有一个先前未鉴定的插入元件。该1634 bp的序列包含一个由504个氨基酸组成的单一ORF,其第三个密码子位置的G+C含量为85%。推测的蛋白质序列与IS231的转座酶有较远的亲缘关系,IS231是插入元件IS4家族的成员。IS1549含有11 bp的末端反向重复序列,其特征是在转座过程中形成异常长且长度可变(71至246 bp)的靶DNA直接重复序列。Southern杂交分析显示,LR222中存在五个IS1549拷贝,但并非所有耻垢分枝杆菌菌株都携带该元件。只有具有与耻垢分枝杆菌607的PCR-限制性片段长度多态性类型相同的65 kDa抗原基因的菌株才含有IS1549。用两组针对IS1549的特异性引物进行PCR检测的其他13种分枝杆菌均未出现预期扩增产物阳性。