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Multi-functional T-DNA/Ds tomato lines designed for gene cloning and molecular and physical dissection of the tomato genome
Authors:Gidoni  D  Fuss  E  Burbidge  A  Speckmann  G-J  James  S  Nijkamp  D  Mett  A  Feiler  J  Smoker  M  de Vroomen  MJ  Leader  D  Liharska  T  Groenendijk  J  Coppoolse  E  Smit  JJM  Levin  I  de Both  M  Schuch  W  Jones  JDG  Taylor  IB  Theres  K  van Haaren  MJJ
Institution:(1) Department of Plant Genetics, Institute of Field Crops, The Volcani Center, P.O. Box 6, Bet Dagan, 50250, Israel;(2) Institute for Genetics, University of Cologne, Cologne, Germany;(3) Max Planck Institute for Plant Breeding Research, Cologne;(4) Department of Physiology and Environmental Science, Sutton Bonington Campus, The University of Nottingham, UK;(5) Keygene N.V., Agro Business Park 90, P.O. Box 216, NL-6700 AE Wageningen, The Netherlands;(6) Zeneca Plant Science, Jealott's Hill Research Station, Bracknell Berkshire, UK;(7) Department of Genetics, Free University of Amsterdam, The Netherlands;(8) Institute for Molecular and Biological Sciences (IMBW), BioCentrum, Amsterdam, The Netherlands;(9) Wheat Improvement Centre, Syngenta, Norwich Research Park, Colney, Norwich, NR4 7UH, UK;(10) CellFor Inc, 355 Burrard Street, Vancouver, British Columbia, V6C 2G8, Canada
Abstract:In order to make the tomato genome more accessible for molecular analysis and gene cloning, we have produced 405 individual tomato (Lycopersicon esculentum) lines containing a characterized copy of pJasm13, a multifunctional T-DNA/modifiedDs transposon element construct. Both the T-DNA and the Ds element in pJasm13 harbor a set of selectable marker genes to monitor excision and reintegration of Ds and additionally, target sequences for rare cutting restriction enzymes (I-PpoI, SfiI, NotI) and for site-specific recombinases (Cre, FLP, R). Blast analysis of flanking genomic sequences of 174 T-DNA inserts revealed homology to transcribed genes in 69 (40%), of which about half are known or putatively identified as genes and ESTs. The map position of 140 individual inserts was determined on the molecular genetic map of tomato. These inserts are distributed over the 12 chromosomes of tomato, allowing targeted and non-targeted transposon tagging, marking of closely linked genes of interest and induction of chromosomal rearrangements including translocations or creation of saturation-deletions or inversions within defined regions linked to the T-DNA insertion site. The different features of pJasm13 were successfully tested in tomato and Arabidopsis thaliana, thus providing a new tool for molecular/genetic dissection studies, including molecular and physical mapping, mutation analysis and cloning strategies in tomato and potentially, in other plants as well.Equal contributors to this workEqual contributors to this workEqual contributors to this workEqual contributors to this workEqual contributors to this workEqual contributors to this workEqual contributors to this workEqual contributors to this workEqual contributors to this workEqual contributors to this workEqual contributors to this workEqual contributors to this work
Keywords:chromosomal rearrangements  site-specific recombination  T-DNA  tomato  transposon
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