Structural analysis of Tn5
- PMID: 6271452
- DOI: 10.1101/sqb.1981.045.01.019
Structural analysis of Tn5
Abstract
Nucleotide sequences have been determined for the 1.5-kb inverted repeats of Tn5 and for their junctions with the central unique region and with host DNA. The primary findings stemming from this analysis are: 1. Integration of Tn5 is accompanied by the duplication of 9 bp of host DNA. 2. Loss of Tn5 occurs by crossover between short, homologous nucleotide sequences near the junction between Tn5 and host DNA. 3. The IR sequences contain long, open translational reading frames that may code for transposase proteins. 4. The two IR sequences differ by a single-base change. This alteration accounts for the two functional differences observed between IRL and IRR: It shortens the reading frame for the transposase gene in IRL, and it improves the efficiency of a promoter for the nearby Km-resistance gene. 5. The NH2 terminus of the structural gene for the Km-resistance gene maps at the very left border of the unique region, i.e., very close to the end of IRL. These results support the view that the inverted repeats of Tn5 stem from two identical copies of an originally independently moving DNA element. In the transposon, one of these, IRL, seems to have evolved toward a close physical and functional linkage with the antibiotic-resistance gene.
Similar articles
-
DNA sequences at the ends of transposon Tn5 required for transposition.Nature. 1983 Jul 21-27;304(5923):280-2. doi: 10.1038/304280a0. Nature. 1983. PMID: 6306482
-
The inverted repeats of Tn5 are functionally different.Cell. 1980 Mar;19(3):795-805. doi: 10.1016/s0092-8674(80)80055-9. Cell. 1980. PMID: 6244898
-
The functional differences in the inverted repeats of Tn5 are caused by a single base pair nonhomology.Cell. 1981 Jan;23(1):191-9. doi: 10.1016/0092-8674(81)90284-1. Cell. 1981. PMID: 6260374
-
The Tn5 transposon.Annu Rev Microbiol. 1993;47:945-63. doi: 10.1146/annurev.mi.47.100193.004501. Annu Rev Microbiol. 1993. PMID: 7504907 Review.
-
Small mobile sequences in bacteria display diverse structure/function motifs.Mol Microbiol. 2008 Feb;67(3):475-81. doi: 10.1111/j.1365-2958.2007.06068.x. Epub 2007 Dec 10. Mol Microbiol. 2008. PMID: 18086200 Free PMC article. Review.
Cited by
-
Siderophore Synthesis Ability of the Nitrogen-Fixing Bacterium (NFB) GXGL-4A is Regulated at the Transcriptional Level by a Transcriptional Factor (trX) and an Aminomethyltransferase-Encoding Gene (amt).Curr Microbiol. 2022 Oct 17;79(12):369. doi: 10.1007/s00284-022-03080-4. Curr Microbiol. 2022. PMID: 36253498
-
Elucidating the Role of Virulence Traits in the Survival of Pathogenic E. coli PI-7 Following Disinfection.Front Bioeng Biotechnol. 2020 Dec 22;8:614186. doi: 10.3389/fbioe.2020.614186. eCollection 2020. Front Bioeng Biotechnol. 2020. PMID: 33415102 Free PMC article.
-
Identification of the Minimal Replicon of Lactococcus lactis subsp. lactis UC317 Plasmid pCI305.Appl Environ Microbiol. 1990 Jan;56(1):202-9. doi: 10.1128/aem.56.1.202-209.1990. Appl Environ Microbiol. 1990. PMID: 16348092 Free PMC article.
-
A novel selenite- and tellurite-inducible gene in Escherichia coli.Appl Environ Microbiol. 2000 Nov;66(11):4972-8. doi: 10.1128/AEM.66.11.4972-4978.2000. Appl Environ Microbiol. 2000. PMID: 11055951 Free PMC article.
-
Recombination in the 5' leader of murine leukemia virus is accurate and influenced by sequence identity with a strong bias toward the kissing-loop dimerization region.J Virol. 1998 Sep;72(9):6967-78. doi: 10.1128/JVI.72.9.6967-6978.1998. J Virol. 1998. PMID: 9696788 Free PMC article.
Publication types
MeSH terms
Substances
Associated data
- Actions
- Actions
LinkOut - more resources
Full Text Sources
Other Literature Sources