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1
Characterization of the left 4 kb of conjugative transposon Tn916: determinants involved in excision.接合转座子Tn916左侧4kb的特性分析:参与切除的决定因素
Plasmid. 1993 Nov;30(3):234-50. doi: 10.1006/plas.1993.1055.
2
Evidence that coupling sequences play a frequency-determining role in conjugative transposition of Tn916 in Enterococcus faecalis.有证据表明,在粪肠球菌中,偶联序列在Tn916的接合转座中发挥频率决定作用。
J Bacteriol. 1994 Jun;176(11):3328-35. doi: 10.1128/jb.176.11.3328-3335.1994.
3
Conjugative transposition: Tn916 integrase contains two independent DNA binding domains that recognize different DNA sequences.接合转座:Tn916整合酶包含两个识别不同DNA序列的独立DNA结合结构域。
EMBO J. 1994 Apr 1;13(7):1541-8. doi: 10.1002/j.1460-2075.1994.tb06416.x.
4
Conjugative transposition of Tn916: preferred targets and evidence for conjugative transfer of a single strand and for a double-stranded circular intermediate.Tn916的接合转座:单链接合转移和双链环状中间体的首选靶标及证据
Mol Microbiol. 1994 Mar;11(6):1099-108. doi: 10.1111/j.1365-2958.1994.tb00386.x.
5
Nucleotide sequence of the 18-kb conjugative transposon Tn916 from Enterococcus faecalis.来自粪肠球菌的18kb接合转座子Tn916的核苷酸序列。
Plasmid. 1994 Nov;32(3):350-4. doi: 10.1006/plas.1994.1077.
6
Tn916 target DNA sequences bind the C-terminal domain of integrase protein with different affinities that correlate with transposon insertion frequency.Tn916靶DNA序列以不同亲和力结合整合酶蛋白的C末端结构域,这些亲和力与转座子插入频率相关。
J Bacteriol. 1995 Apr;177(8):1938-46. doi: 10.1128/jb.177.8.1938-1946.1995.
7
Location and characteristics of the transfer region of a Bacteroides conjugative transposon and regulation of transfer genes.拟杆菌属接合转座子转移区域的位置与特征及转移基因的调控
J Bacteriol. 1995 Sep;177(17):4992-9. doi: 10.1128/jb.177.17.4992-4999.1995.
8
Unconstrained bacterial promiscuity: the Tn916-Tn1545 family of conjugative transposons.不受限制的细菌滥交:接合转座子Tn916 - Tn1545家族
Trends Microbiol. 1995 Jun;3(6):229-36. doi: 10.1016/s0966-842x(00)88930-1.
9
Streptococcal plasmid pIP501 has a functional oriT site.链球菌质粒pIP501有一个功能性的转移起始位点。
J Bacteriol. 1995 Aug;177(15):4199-206. doi: 10.1128/jb.177.15.4199-4206.1995.
10
Recombination-deficient mutant of Streptococcus faecalis.粪肠球菌重组缺陷突变体
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接合转座子Tn916上转移功能起始位点(oriT)

A functional origin of transfer (oriT) on the conjugative transposon Tn916.

作者信息

Jaworski D D, Clewell D B

机构信息

Department of Biologic and Materials Sciences, School of Dentistry, University of Michigan, Ann Arbor 48109, USA.

出版信息

J Bacteriol. 1995 Nov;177(22):6644-51. doi: 10.1128/jb.177.22.6644-6651.1995.

DOI:10.1128/jb.177.22.6644-6651.1995
PMID:7592445
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC177520/
Abstract

The origin of transfer (oriT) of the 18-kb conjugative transposon Tn916 has been localized to a 466-bp region which spans nucleotides 15215 to 15681 on the transposon map. The oriT lies within an intercistronic region between open reading frames ORF20 and ORF21 that contains six sets of inverted repeats ranging from 10 to 20 bp in size. The segment contains three sequences showing identity in 9 of 12 bp to the consensus nicking site (nic) of the IncP family of conjugative plasmids found in gram-negative bacteria. Overlapping one of these sequences is a region similar to the nic site of the F plasmid. Functionality was based on the ability of the oriT-containing sequence to provide a cis-acting mobilization of chimeras involving the shuttle vector pWM401 in response to activation in trans by an intact chromosome-borne transposon Tn916 delta E. Cloned segments of 466 or 376 nucleotides resulted in unselected cotransfer of the plasmid at levels of about 40% when selection was for Tn916 delta E, whereas a 110-bp segment resulted in cotransfer at a frequency of about 7%. Mobilization was specific in that gram-positive plasmids, such as pAD1 and pAM beta 1, and the gram-negative plasmids pOX38 (a derivative of F) and RP1 did not mobilize oriT-containing chimeras.

摘要

18kb 接合转座子 Tn916 的转移起始点(oriT)已定位到一个 466bp 的区域,该区域在转座子图谱上跨越核苷酸 15215 至 15681。oriT 位于开放阅读框 ORF20 和 ORF21 之间的基因间区域内,该区域包含六组大小从 10 到 20bp 的反向重复序列。该片段包含三个序列,在 12 个碱基中有 9 个与革兰氏阴性菌中发现的 IncP 家族接合质粒的共有切口位点(nic)具有同一性。其中一个序列重叠的区域类似于 F 质粒的 nic 位点。功能性基于含 oriT 序列能够响应完整染色体携带的转座子 Tn916 delta E 的反式激活,为涉及穿梭载体 pWM401 的嵌合体提供顺式作用的动员。当选择 Tn916 delta E 时,466 或 376 个核苷酸的克隆片段导致质粒在约 40%的水平上进行未选择的共转移,而 110bp 的片段导致共转移频率约为 7%。动员具有特异性,因为革兰氏阳性质粒,如 pAD1 和 pAM beta 1,以及革兰氏阴性质粒 pOX38(F 的衍生物)和 RP1 不会动员含 oriT 的嵌合体。