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Functional Plant Biology Functional Plant Biology Society
Plant function and evolutionary biology
RESEARCH ARTICLE

The maize Activator/Dissociation system is functional in hexaploid wheat through successive generations

Gabriela M. Pastori A , Alison Huttly A , Jevon West A , Caroline Sparks A , Alejandro Pieters B , Celina M. Luna C , Huw D. Jones A and Christine H. Foyer D E
+ Author Affiliations
- Author Affiliations

A Crop Performance and Improvement Division, Rothamsted Research, Harpenden, Hertfordshire AL5 2JQ, UK.

B IVI, Centro de Ecología, Altos de Pipe, Carretera Panamericana Km 11, Apartado 21827, Caracas 1020-A, Venezuela.

C Instituto de Fitopatología y FisiologíaVegetal (IFFIVE)-INTA, Camino 60 cuadras Km 51/2, 5009 Cordoba, Argentina.

D School of Agriculture, Food and Rural Development, Agriculture Building, Newcastle University, Newcastle upon Tyne NE1 7RU, UK.

E Corresponding author. Email: christine.foyer@newcastle.ac.uk

Functional Plant Biology 34(9) 835-843 https://doi.org/10.1071/FP07112
Submitted: 2 May 2007  Accepted: 3 July 2007   Published: 30 August 2007

Abstract

The aim of the present study was to provide useful background information and evidence of the functionality of the maize Activator/Dissociation (Ac/Ds) system in hexaploid wheat. Two transgenic parental wheat lines, one harbouring the immobilised Ac element (iAc) and the other the Ds element (pUbi[Ds-uidA]bar), were crossed. Transient GUS assays confirmed that the iAc transposase is active in hexaploid wheat. Selected F1 and F2 lines were analysed by PCR using primers specific to Ac, uidA and bar genes. The primer pair Ubi/bar-tag was used to detect excision of the Ds-uidA sequence, which occurred at a frequency of 39% in the F1 generation. Lines free of Ac and showing evidence of Ds excision were subject to Southern analysis, which indicated that at least one transposition event might have occurred in these lines. Although more evidence is required to unequivocally support the reintegration of the Ds element in the wheat genome, the evidence presented here nevertheless demonstrates the effectiveness and potential value of using this system to tag genes in wheat.


Acknowledgements

Rothamsted Research receives grant-aided support from the Biotechnology and Biological Sciences Research Council (BBSRC) of the United Kingdom. A. Pieters and C. M. Luna acknowledge short-term Royal Society fellowships. The authors thank Professor Peggy G. Lemaux (Berkeley University, USA) for the generous gift of constructs containing the maize Ac element and Act1(DsBar)uidA, Drs Sancha Salgueiro and Martin Cannell for helpful discussions and Nickerson’s Seeds for valuable advice on wheat crossings. The authors are grateful to Professors Narayana Upadhyaya, Bob Furbank, Tony Pryor, Mick Ayliffe (CSIRO, Canberra) and Professor Jonathan Jones (John Innes Centre, UK) for critical reading of the manuscript.


References


Altmann T, Felix G, Jessop A, Kauschmann A, Uwer U, Penacortes H, Willmitzer L (1995) Ac/Ds transposon mutagenesis in Arabidopsis thaliana - mutant spectrum and frequency of Ds insertion mutants. Molecular & General Genetics 247, 646–652.
Crossref | GoogleScholarGoogle Scholar | open url image1

Ayliffe MA, Pallotta M, Langridge P, Pryor AJ (2007) A barley activation tagging system. Plant Molecular Biology 64, 329–347.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Balcells L, Coupland G (1994) The presence of enhancers adjacent to the Ac promoter increases the abundance of transposable messenger-RNA and alters the timing of Ds excision in Arabidopsis. Plant Molecular Biology 24, 789–798.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Bevan MW, Flavell RB, Chilton MD (1983) A chimaeric antibiotic-resistance gene as a selectable marker for plant-cell transformation. Nature 304, 184–187.
Crossref | GoogleScholarGoogle Scholar | open url image1

Chin HG, Choe MS, Lee SH, Park SH, Park SH , et al. (1999) Molecular analysis of rice plants harboring an Ac/Ds transposable element-mediated gene trapping system. The Plant Journal 19, 615–623.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Christensen AH, Quail PH (1996) Ubiquitin promoter-based vectors for high-level expression of selectable and/or screenable marker genes in monocotyledonous plants. Transgenic Research 5, 213–218.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Chuck G, Robbins T, Nijjar C, Ralston E, Courtney Gutterson N, Dooner HK (1993) Tagging and cloning of a petunia flower color gene with the maize transposable element Activator. The Plant Cell 5, 371–378.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Enoki H, Izawa T, Kawahara M, Komatsu M, Koh S, Kyozuka J, Shimamoto K (1999) Ac as a tool for the functional genomics of rice. The Plant Journal 19, 605–613.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Evans LT, Fischer RA (1999) Yield potential: its definition, measurement and significance. Crop Science 39, 1544–1551. open url image1

Faris JD, Haen KM, Gill BS (2000) Saturation mapping of a gene-rich recombination hot spot region in wheat. Genetics 154, 823–835.
PubMed |
open url image1

Fedoroff NV (1989) About maize transposable elements and development. Cell 56, 181–191.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Feuillet C, Keller B (1999) High gene density is conserved at syntenic loci of small and large grass genomes. Proceedings of the National Academy of Sciences of the United States of America 96, 8265–8270.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Gill KS, Gill BS, Endo TR, Boyko EV (1996) Identification and high-density mapping of gene-rich regions in chromosome group 5 of wheat. Genetics 143, 1001–1012.
PubMed |
open url image1

Greco R, Ouwerkerk PBF, Taal AJC, Favalli C, Beguiristain T, Puigdomenech P, Colombo L, Hoge JHC, Pereira A (2001) Early and multiple Ac transpositions in rice suitable for efficient insertional mutagenesis. Plant Molecular Biology 46, 215–227.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Greco R, Ouwerkerk PBF, de Kam RJ, Sallaud C, Favalli C, Colombo L, Guiderdoni E, Meijer AH, Hoge JHC, Pereira A (2003) Transpositional behaviour of an Ac/Ds system for reverse genetics in rice. Theoretical and Applied Genetics 108, 10–24.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Izawa T, Ohnishi T, Nakano T, Ishida N, Enoki H , et al. (1997) Transposon tagging in rice. Plant Molecular Biology 35, 219–229.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Jefferson R (1987) Assaying chimeric genes in plants: the GUS gene fusion system. Plant Molecular Biology Reporter 5, 387–405. open url image1

Jeon JS, An GH (2001) Gene tagging in rice: a high throughput system for functional genomics. Plant Science 161, 211–219.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Jones DA, Thomas CM, Hammond-Kosack KE, Balintkurti PJ, Jones JDG (1994) Isolation of the tomato CF-9 gene for resistance to Cladosporum fulvum by transposon tagging. Science 266, 789–793.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Jones JDG, Carland FM, Maliga P, Dooner H (1989) Visual detection of transposition of the maize element Activator (Ac) in tobacco seedlings. Science 244, 204–207.
Crossref | GoogleScholarGoogle Scholar | open url image1

Koprek T, McElroy D, Louwerse J, Williams-Carrier R, Lemaux P (2000) An efficient method for dispersing Ds elements in the barley genome as a tool for determining gene function. The Plant Journal 24, 253–263.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Lawrence GJ, Finnegan EJ, Ayliffe MA, Ellis JG (1995) The L6 gene for flax rust resistance is related to the Arabidopsis bacterial-resistance gene RPS2 and the tobacco viral resistance gene-N. The Plant Cell 7, 1195–1206.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

McElroy D, Louwerse J, McElroy S, Lemaux P (1997) Development of a simple transient assay for Ac/Ds activity in cells of intact barley tissue. The Plant Journal 11, 157–165.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Moore G (2000) Cereal chromosome structure, evolution, and pairing. Annual Review of Plant Physiology 51, 195–222.
Crossref | GoogleScholarGoogle Scholar | open url image1

Muller E, Lorz H, Lutticke S (1996) Variability of transgene expression in clonal cell lines of wheat. Plant Science 114, 71–82.
Crossref | GoogleScholarGoogle Scholar | open url image1

Nakagawa Y, Machida C, Machida Y, Toriyama K (2000) Frequency and pattern of transposition of the maize transposable element Ds in transgenic rice plants. Plant & Cell Physiology 41, 733–742.
PubMed |
open url image1

Olivares-Villegas JJ, Reynolds MP, McDonald GK (2007) Drought-adaptive attributes in the Seri-Babax hexaploid wheat population. Functional Plant Biology 34, 189–203.
Crossref | GoogleScholarGoogle Scholar | open url image1

Pastori GM, Wilkinson MD, Steele SH, Sparks CA, Jones HD, Parry MAJ (2001) Age-dependent transformation frequency in elite wheat varieties. Journal of Experimental Botany 52, 857–863.
PubMed |
open url image1

Sabelli P , Shewry PR (1995) Gene characterization by Southern analysis. In ‘Methods in molecular biology, vol. 49. Plant gene transfer and expression protocols’. (Ed. H. Jones) pp. 161–180. (Humana Press: Totowa, NJ)

Salgueiro S, Matthes M, Gil J, Steele S, Savazzini F, Riley A, Jones HD, Lazzeri PA, Barcelo P (2002) Insertional tagging of regulatory sequences in tritordeum; a hexaploid cereal species. Theoretical and Applied Genetics 104, 916–925.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Sambrook J , Fritsch EF , Maniatis T (1989). ‘Molecular Cloning, 2nd edn.’ (Cold Spring Harbor Laboratory Press: Cold Spring Harbor, NY)

Smith DB, Flavell RB (1975) Characterisation of the wheat genome by renaturation kinetics. Chromosoma 50, 223–242.
Crossref | GoogleScholarGoogle Scholar | open url image1

Stacey J, Isaac P (1994) Isolation of DNA from plants. In ‘Methods in molecular biology – protocols for nucleic acid analysis by non-radioactive probes’. (Ed. P Isaac) pp. 9–15. (Humana Press: Totowa, NJ)

Takumi S, Murai K, Mori N, Nakamura C (1999) Trans-activation of a maize Ds transposable element in transgenic wheat plants expressing the Ac transposase gene. Theoretical and Applied Genetics 98, 947–953.
Crossref | GoogleScholarGoogle Scholar | open url image1

Upadhyaya NM, Zhou X-R, Ramm K, Zhu Q-H, Wu L , et al. (2002) An iAc/Ds gene and enhancer trapping system for insertional mutagenesis in rice. Functional Plant Biology 29, 547–559.
Crossref | GoogleScholarGoogle Scholar | open url image1

Wendel JF (2000) Genome evolution in polyploids. Plant Molecular Biology 42, 225–249.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Whitham S, Dineshkumar SP, Choi D, Hehl R, Corr C, Baker B (1994) The product of the tobacco mosaic-virus resistance gene N – similarity to Toll and the Interleukin-1 receptor. Cell 78, 1101–1115.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Wohlleben W, Arnold W, Broer I, Hillemann D, Strauch E, Puhler A (1988) Nucleotide-sequence of the phosphinothricin N-acetyltransferase gene from Streptomyces viridochromogenes-Tu494 and its expression in Nicotiana tabacum. Gene 70, 25–37.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Yuan Q, Hill J, Hsiao J, Moffat K, Ouyang S, Cheng Z, Jiang J, Buell CR (2002) Genome sequencing of a 239-kb region of rice chromosome 10L reveals a high frequency of gene duplication and a large chloroplast DNA insertion. Molecular Genetics and Genomics 267, 713–720.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1