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PMID: 1323365 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Promoter fusions to the Activator transposase gene cause distinct patterns of Dissociation excision in tobacco cotyledons.

The Plant cell ·Vol. 4 ·No. 5 ·1992-05-00 ·Pages 573-82

Scofield SR, Harrison K, Nurrish SJ, Jones JD

Abstract

To explore the effects of altering the level of Activator (Ac) transposase (TPase) expression, a series of plasmids was constructed in which heterologous promoters were fused to the TPase gene. Promoters for the cauliflower mosaic virus (CaMV) 35S transcript and the octopine synthase (ocs) and nopaline synthase (nos) genes were tested. These fusions, and constructs expressing TPase from the wild-type Ac promoter, were introduced into tobacco, and their activity was monitored by crossing to a line carrying Dissociation (Ds) in a streptomycin phosphotransferase gene (Ds::SPT). The SPT marker provides a record of somatic excisions of Ds that occur during embryo development. The patterns of somatic variegation that resulted from transactivation by each fusion were distinct and strikingly different from the pattern triggered by the wild-type Ac constructs. Unlike wild-type Ac, which caused transposition throughout embryo development, each fusion gave rise to sectors of discrete size. Sectors triggered by the CaMV 35S fusion were largest, ocs sectors were intermediate, and nos were smallest. These patterns appear to indicate differential timing of the activation of these promoters during embryogeny. Measurement of transcript abundance for each transformant indicated that the CaMV 35S-transformed plants accumulated approximately 1000-fold more TPase mRNA than plants containing wild-type Ac, whereas ocs- and nos-transformed lines accumulated about 100-fold and 20-fold higher levels, respectively. Measurements of germinal excision frequencies driven by the chimeric TPase fusions, however, indicated that increasing transcription does not necessarily result in an increase in germinal excision. These measurements showed that the ocs and nos fusions have very low rates of germinal excision. Only the CaMV 35S fusion transformants were found to have higher rates than the Ac constructs, although significant pod-to-pod variation was observed. Gel blot analysis of DNA from progeny carrying germinal excision events resulting from the CaMV 35S fusion showed that excision is associated with reinsertion and that siblings sometimes carry the same transposition events. These findings suggest that in tobacco there is no direct proportionality between TPase expression and Ac-Ds transposition activity. This possibility has important implications for understanding the regulation of Ac transposition and for designing efficient gene tagging systems.

Related Genes
Ac
MeSH Terms
Base Sequence Cloning, Molecular DNA DNA Transposable Elements Gene Expression Regulation Molecular Sequence Data Mosaic Viruses/genetics Nucleic Acid Hybridization Nucleotidyltransferases/genetics Phenotype Plants, Toxic Promoter Regions, Genetic RNA, Messenger/genetics Ribonucleases/metabolism Tobacco/enzymology,genetics Transposases
Chemicals
DNA Transposable Elements RNA, Messenger DNA Nucleotidyltransferases Transposases Ribonucleases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Scofield S R
Sainsbury Laboratory, John Innes Centre, Norwich, United Kingdom.
Harrison K
Nurrish S J
Jones J D
References (23)
23 references, click to expand
  1. Properties of the maize transposable element Activator in transgenic tobacco plants: a versatile inter-species genetic tool.
    Plant Cell. 1990 Aug;2(8):709-21 PMID: 1967055
  2. Replication of an origin-containing derivative of plasmid RK2 dependent on a plasmid function provided in trans.
    Proc Natl Acad Sci U S A. 1979 Apr;76(4):1648-52 PMID: 377280
  3. Improved expression of streptomycin resistance in plants due to a deletion in the streptomycin phosphotransferase coding sequence.
    Mol Gen Genet. 1988 Nov;214(3):456-9 PMID: 2851095
  4. The 5'-leader sequence of tobacco mosaic virus RNA enhances the expression of foreign gene transcripts in vitro and in vivo.
    Nucleic Acids Res. 1987 Apr 24;15(8):3257-73 PMID: 3575095
  5. Identification of DNA sequences required for activity of the cauliflower mosaic virus 35S promoter.
    Nature. 1985 Feb 28-Mar 6;313(6005):810-2 PMID: 3974711
  6. Nopaline synthase: transcript mapping and DNA sequence.
    J Mol Appl Genet. 1982;1(6):561-73 PMID: 7153689
  7. High level expression of introduced chimaeric genes in regenerated transformed plants.
    EMBO J. 1985 Oct;4(10):2411-8 PMID: 15929216
  8. Elevated levels of Activator transposase mRNA are associated with high frequencies of Dissociation excision in Arabidopsis.
    Plant Cell. 1992 May;4(5):583-95 PMID: 1323366
  9. Preferential transposition of the maize element Activator to linked chromosomal locations in tobacco.
    Plant Cell. 1990 Aug;2(8):701-7 PMID: 1967054
  10. Clonal analysis of the cell lineages in the male flower of maize.
    Dev Biol. 1990 Nov;142(1):233-45 PMID: 2172058
  11. Sequences near the termini are required for transposition of the maize transposon Ac in transgenic tobacco plants.
    Proc Natl Acad Sci U S A. 1989 Dec;86(23):9385-8 PMID: 2556710
  12. Studies on the introduction and mobility of the maize Activator element in Arabidopsis thaliana and Daucus carota.
    EMBO J. 1987 Dec 20;6(13):3881-9 PMID: 2832144
  13. A chromosome replication pattern deduced from pericarp phenotypes resulting from movements of the transposable element, modulator, in maize.
    Genetics. 1984 Oct;108(2):471-85 PMID: 17246235
  14. Visual detection of transposition of the maize element activator (ac) in tobacco seedlings.
    Science. 1989 Apr 14;244(4901):204-7 PMID: 17835353
  15. GUS fusions: beta-glucuronidase as a sensitive and versatile gene fusion marker in higher plants.
    EMBO J. 1987 Dec 20;6(13):3901-7 PMID: 3327686
  16. Rapid and efficient site-specific mutagenesis without phenotypic selection.
    Proc Natl Acad Sci U S A. 1985 Jan;82(2):488-92 PMID: 3881765
  17. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.
    Anal Biochem. 1983 Jul 1;132(1):6-13 PMID: 6312838
  18. Nucleotide sequence and transcript map of the Agrobacterium tumefaciens Ti plasmid-encoded octopine synthase gene.
    J Mol Appl Genet. 1982;1(6):499-511 PMID: 7153687
  19. Chromosome organization and genic expression.
    Cold Spring Harb Symp Quant Biol. 1951;16:13-47 PMID: 14942727
  20. Isolation of a dual plant promoter fragment from the Ti plasmid of Agrobacterium tumefaciens.
    EMBO J. 1984 Dec 1;3(12):2723-30 PMID: 16453574
  21. Transposition of the maize controlling element "Activator" in tobacco.
    Proc Natl Acad Sci U S A. 1986 Jul;83(13):4844-8 PMID: 16593722
  22. A simple and general method for transferring genes into plants.
    Science. 1985 Mar 8;227(4691):1229-31 PMID: 17757866
  23. The putative transposase of transposable element Ac from Zea mays L. interacts with subterminal sequences of Ac.
    EMBO J. 1989 Nov;8(11):3177-85 PMID: 2555157
Article Info
Journal
The Plant cell
Abbr.
Plant Cell
ISSN
1040-4651
Published
1992-05-00
Pages
573-82
Language
English
Region
England
NLM ID
9208688
PMCID
PMC160154
Subset
IM
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