The tetracycline resistance transposons Tn1721 and Tn1771 have three 38-base-pair repeats and generate five-base-pair direct repeats

Schöffl F, Arnold W, Pühler A, Altenbuchner J, Schmitt R (1981)
Mol Gen Genet 181(1): 87-94.

Download
No fulltext has been uploaded. References only!
DOI
Journal Article | Original Article | Published | English

No fulltext has been uploaded

Author
; ; ; ;
Department
Fakultät für Biologie
Publishing Year
1981
ISSN
0026-8925
eISSN
1617-4623
PUB-ID

Cite this

Schöffl F, Arnold W, Pühler A, Altenbuchner J, Schmitt R. The tetracycline resistance transposons Tn1721 and Tn1771 have three 38-base-pair repeats and generate five-base-pair direct repeats. Mol Gen Genet. 1981;181(1):87-94.
Schöffl, F., Arnold, W., Pühler, A., Altenbuchner, J., & Schmitt, R. (1981). The tetracycline resistance transposons Tn1721 and Tn1771 have three 38-base-pair repeats and generate five-base-pair direct repeats. Mol Gen Genet, 181(1), 87-94. doi:10.1007/BF00339010
Schöffl, F., Arnold, W., Pühler, A., Altenbuchner, J., and Schmitt, R. (1981). The tetracycline resistance transposons Tn1721 and Tn1771 have three 38-base-pair repeats and generate five-base-pair direct repeats. Mol Gen Genet 181, 87-94.
Schöffl, F., et al., 1981. The tetracycline resistance transposons Tn1721 and Tn1771 have three 38-base-pair repeats and generate five-base-pair direct repeats. Mol Gen Genet, 181(1), p 87-94.
F. Schöffl, et al., “The tetracycline resistance transposons Tn1721 and Tn1771 have three 38-base-pair repeats and generate five-base-pair direct repeats”, Mol Gen Genet, vol. 181, 1981, pp. 87-94.
Schöffl, F., Arnold, W., Pühler, A., Altenbuchner, J., Schmitt, R.: The tetracycline resistance transposons Tn1721 and Tn1771 have three 38-base-pair repeats and generate five-base-pair direct repeats. Mol Gen Genet. 181, 87-94 (1981).
Schöffl, F, Arnold, Walter, Pühler, Alfred, Altenbuchner, J, and Schmitt, R. “The tetracycline resistance transposons Tn1721 and Tn1771 have three 38-base-pair repeats and generate five-base-pair direct repeats”. Mol Gen Genet 181.1 (1981): 87-94.
This data publication is cited in the following publications:
This publication cites the following data publications:

44 Citations in Europe PMC

Data provided by Europe PubMed Central.

blaCTX-M-65 is carried by a Tn1722-like element on an IncN conjugative plasmid of ST131 Escherichia coli.
Zong Z, Yu R, Wang X, Lu X., J. Med. Microbiol. 60(Pt 4), 2011
PMID: 21163826
Identification of a truncated Tn1721-like transposon located on a small plasmid of Escherichia coli isolated from Varanus indicus.
Waturangi DE, Schwarz S, Suwanto A, Kehrenberg C, Erdelen W., J. Vet. Med. B Infect. Dis. Vet. Public Health 50(2), 2003
PMID: 12675900
Transposon Tn1721 distribution among strains of Xylella fastidiosa.
Ferreira LP, Lemos EG, Lemos MV., FEMS Microbiol. Lett. 208(2), 2002
PMID: 11959431
The Sinorhizobium meliloti nutrient-deprivation-induced tyrosine degradation gene hmgA is controlled by a novel member of the arsR family of regulatory genes.
Milcamps A, Struffi P, de Bruijn FJ., Appl. Environ. Microbiol. 67(6), 2001
PMID: 11375175
Plasmid-encoded tetracycline resistance in Salmonella enterica subsp. enterica serovars choleraesuis and typhimurium: identification of complete and truncated Tn1721 elements.
Frech G, Schwarz S., FEMS Microbiol. Lett. 176(1), 1999
PMID: 10418136
Tetracycline resistance in Salmonella enterica subsp. enterica serovar Dublin.
Frech G, Schwarz S., Antimicrob. Agents Chemother. 42(5), 1998
PMID: 9593170
The use of an improved transposon mutagenesis system for DNA sequencing leads to the characterization of a new insertion sequence of Streptomyces lividans 66.
Fischer J, Maier H, Viell P, Altenbuchner J., Gene 180(1-2), 1996
PMID: 8973350
Abundance of Tn3, Tn21, and Tn501 transposase (tnpA) sequences in bacterial community DNA from marine environments.
Dahlberg C, Hermansson M., Appl. Environ. Microbiol. 61(8), 1995
PMID: 7487037
Effects of variation of inverted-repeat sequences on reactions mediated by the transposase of Tn21.
Martin C, Grinsted J, de la Cruz F., J. Bacteriol. 171(7), 1989
PMID: 2544566
Factors that affect transposition mediated by the Tn21 transposase.
Grinsted J, Martin C, de la Cruz F., Plasmid 20(1), 1988
PMID: 2853879
The Clostridium perfringens chloramphenicol resistance transposon Tn4451 excises precisely in Escherichia coli.
Abraham LJ, Rood JI., Plasmid 19(2), 1988
PMID: 2901770
Tn3-like elements: molecular structure, evolution.
Lett MC., Biochimie 70(2), 1988
PMID: 2840127
Biochemical and genetic characterization of the tet determinant of Bacillus plasmid pAB124.
Eccles SJ, Chopra I., J. Bacteriol. 158(1), 1984
PMID: 6325384
Resolution of a hybrid cointegrate between transposons Tn501 and Tn1721 defines the recombination site.
Rogowsky P, Schmitt R., Mol. Gen. Genet. 193(1), 1984
PMID: 6318048
Circularized copies of amplifiable resistance genes from Haemophilus influenzae plasmids.
Spies T, Laufs R., J. Bacteriol. 156(3), 1983
PMID: 6315683
Amplification of resistance genes in Haemophilus influenzae plasmids.
Spies T, Laufs R, Riess FC., J. Bacteriol. 155(2), 1983
PMID: 6307983
Evidence for a plasmid in a methanogenic bacterium.
Thomm M, Altenbuchner J, Stetter KO., J. Bacteriol. 153(2), 1983
PMID: 6296038
Characterization of the transposons Tn1822 (Tc) and Tn1824 (TpSm) and the light they throw on the natural spread of resistance genes.
Tietze E, Prager R, Tschape H., Plasmid 8(3), 1982
PMID: 6294709
Insertion sites and the terminal nucleotide sequences of the Tn4 transposon.
Hyde DR, Tu CP., Nucleic Acids Res. 10(13), 1982
PMID: 6287429

39 References

Data provided by Europe PubMed Central.

Organization of a hybrid between phage f1 and plasmid pSC101.
Ravetch JV, Ohsumi M, Model P, Vovis GF, Fischhoff D, Zinder ND., Proc. Natl. Acad. Sci. U.S.A. 76(5), 1979
PMID: 287058
Transposition of the Escherichia coli insertion element gamma generates a five-base-pair repeat.
Reed RR, Young RA, Steitz JA, Grindley ND, Guyer MS., Proc. Natl. Acad. Sci. U.S.A. 76(10), 1979
PMID: 388421

R, 1973
Characterisation of Tn1721, a new transposon containing tetracycline resistance genes capable of amplification.
Schmitt R, Bernhard E, Mattes R., Mol. Gen. Genet. 172(1), 1979
PMID: 377024

AUTHOR UNKNOWN, 0

F, 1977

F, 1979
Intramolecular amplification of the tetracycline resistance determinant of transposon Tn1771 in Escherichia coli.
Schoffl F, Puhler A., Genet. Res. 33(3), 1979
PMID: 387525
The plasmid system of Escherichia coli strain UR12644: identification and molecular characteristics of transposons involved in the generation of endogenous R-plasmids.
Schoffl F, Puhler A., Genet. Res. 34(3), 1979
PMID: 232453
Nucleotide sequence of cro, cII and part of the O gene in phage lambda DNA.
Schwarz E, Scherer G, Hobom G, Kossel H., Nature 272(5652), 1978
PMID: 264238
Electron microscopy of DNA: determination of absolute molecular weights and linear density.
Stuber D, Bujard H., Mol. Gen. Genet. 154(3), 1977
PMID: 927439
pBR322 restriction map derived from the DNA sequence: accurate DNA size markers up to 4361 nucleotide pairs long.
Sutcliffe JG., Nucleic Acids Res. 5(8), 1978
PMID: 358147
Construction of a colicin E1-R factor composite plasmid in vitro: means for amplification of deoxyribonucleic acid.
Tanaka T, Weisblum B., J. Bacteriol. 121(1), 1975
PMID: 1090574
Plasmid-determined tetracycline resistance in Streptococcus faecalis: tandemly repeated resistance determinants in amplified forms of pAMalpha1 DNA.
Yagi Y, Clewell DB., J. Mol. Biol. 102(3), 1976
PMID: 818395

Export

0 Marked Publications

Open Data PUB

Web of Science

View record in Web of Science®

Sources

PMID: 6261087
PubMed | Europe PMC

Search this title in

Google Scholar