Literature DB >> 2543983

Frameshifting is required for production of the transposase encoded by insertion sequence 1.

Y Sekine1, E Ohtsubo.   

Abstract

Insertion sequence IS1 has two coding frames, insA and insB, which are essential for its transposition. Here, we show that a frameshifting event in the -1 direction from the 3' end region of the insA frame to an open reading frame (B' frame), extending from the 5' end of the insB frame, is involved in production of the InsA-B'-InsB fusion protein that has IS1 transposase activity. The frameshifting event is likely to have occurred at the sequence AAAAAC where the insA frame overlaps the B' frame. Interestingly, this sequence is also present in one of the two sequences identified in retroviruses as frameshift signals for production of transframe polyproteins from the overlapping genes gag-pro or gag-pro-pol.

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Year:  1989        PMID: 2543983      PMCID: PMC287320          DOI: 10.1073/pnas.86.12.4609

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  39 in total

1.  Plasmids containing insertion elements are potential transposons.

Authors:  E Ohtsubo; M Zenilman; H Ohtsubo
Journal:  Proc Natl Acad Sci U S A       Date:  1980-02       Impact factor: 11.205

2.  Complete nucleotide sequence of an infectious clone of human T-cell leukemia virus type II: an open reading frame for the protease gene.

Authors:  K Shimotohno; Y Takahashi; N Shimizu; T Gojobori; D W Golde; I S Chen; M Miwa; T Sugimura
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

3.  The gag and pol genes of bovine leukemia virus: nucleotide sequence and analysis.

Authors:  N R Rice; R M Stephens; A Burny; R V Gilden
Journal:  Virology       Date:  1985-04-30       Impact factor: 3.616

4.  DNA sequence at the end of IS1 required for transposition.

Authors:  P Gamas; D Galas; M Chandler
Journal:  Nature       Date:  1985 Oct 3-9       Impact factor: 49.962

5.  Complete nucleotide sequence of a milk-transmitted mouse mammary tumor virus: two frameshift suppression events are required for translation of gag and pol.

Authors:  R Moore; M Dixon; R Smith; G Peters; C Dickson
Journal:  J Virol       Date:  1987-02       Impact factor: 5.103

6.  Electron microscopy of polar insertions in the lac operon of Escherichia coli.

Authors:  M H Malamy; M Fiandt; W Szybalski
Journal:  Mol Gen Genet       Date:  1972

7.  Polar mutations in lac, gal and phage lambda consist of a few IS-DNA sequences inserted with either orientation.

Authors:  M Fiandt; W Szybalski; M H Malamy
Journal:  Mol Gen Genet       Date:  1972

8.  Repression of cointegration ability of insertion element IS1 by transcriptional readthrough from flanking regions.

Authors:  C Machida; Y Machida; H C Wang; K Ishizaki; E Ohtsubo
Journal:  Cell       Date:  1983-08       Impact factor: 41.582

9.  On the role of IS1 in the formation of hybrids between the bacteriophage P1 and the R plasmid NR1.

Authors:  S Iida; W Arber
Journal:  Mol Gen Genet       Date:  1980-01

10.  Signals for ribosomal frameshifting in the Rous sarcoma virus gag-pol region.

Authors:  T Jacks; H D Madhani; F R Masiarz; H E Varmus
Journal:  Cell       Date:  1988-11-04       Impact factor: 41.582

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  67 in total

1.  Involvement of H-NS in transpositional recombination mediated by IS1.

Authors:  Y Shiga; Y Sekine; Y Kano; E Ohtsubo
Journal:  J Bacteriol       Date:  2001-04       Impact factor: 3.490

2.  Reactivation of insertionally inactivated Shiga toxin 2 genes of Escherichia coli O157:H7 caused by nonreplicative transposition of the insertion sequence.

Authors:  M Kusumoto; Y Nishiya; Y Kawamura
Journal:  Appl Environ Microbiol       Date:  2000-03       Impact factor: 4.792

3.  Presence of a characteristic D-D-E motif in IS1 transposase.

Authors:  Shinya Ohta; Ken Tsuchida; Sunju Choi; Yasuhiko Sekine; Yasuyuki Shiga; Eiichi Ohtsubo
Journal:  J Bacteriol       Date:  2002-11       Impact factor: 3.490

4.  Protective role for H-NS protein in IS1 transposition.

Authors:  Claudine Rouquette; Marie-Claude Serre; David Lane
Journal:  J Bacteriol       Date:  2004-04       Impact factor: 3.490

5.  Evidence for a hybrid genomic island in verocytotoxin-producing Escherichia coli CL3 (serotype O113:H21) containing segments of EDL933 (serotype O157:H7) O islands 122 and 48.

Authors:  Songhai Shen; Mariola Mascarenhas; Kris Rahn; James B Kaper; Mohamed A Karmali; Mohamed A Karmal
Journal:  Infect Immun       Date:  2004-03       Impact factor: 3.441

6.  Identification, DNA sequence, and distribution of IS981, a new, high-copy-number insertion sequence in lactococci.

Authors:  K M Polzin; L L McKay
Journal:  Appl Environ Microbiol       Date:  1991-03       Impact factor: 4.792

7.  Factors determining the frequency of plasmid cointegrate formation mediated by insertion sequence IS3 from Escherichia coli.

Authors:  J Spielmann-Ryser; M Moser; P Kast; H Weber
Journal:  Mol Gen Genet       Date:  1991-05

8.  Unusual codon bias occurring within insertion sequences in Escherichia coli.

Authors:  J G Lawrence; D L Hartl
Journal:  Genetica       Date:  1991       Impact factor: 1.082

9.  Partial correction of a severe molecular defect in hemophilia A, because of errors during expression of the factor VIII gene.

Authors:  M Young; H Inaba; L W Hoyer; M Higuchi; H H Kazazian; S E Antonarakis
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

10.  Antigenic variation in Mycoplasma hyorhinis: increased repertoire of variable lipoproteins expanding surface diversity and structural complexity.

Authors:  R Rosengarten; P M Theiss; D Yogev; K S Wise
Journal:  Infect Immun       Date:  1993-05       Impact factor: 3.441

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