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INRA-Versailles lines

Donated by

  • Georges Pelletier Station de Génétique et d’Amélioration des Plantes , Institut Jean-Pierre Bourgin (IJPB), Institut National de la Recherche Agronomique (INRA)

Click here to view all 10481 of these lines.


INRA-Versailles T-DNA lines

Station de Genetique et d'Amelioration des plantes, INRA, 78026 Versailles cedex, France

Sets in this collection

Nasc code Description Set contents
N5388 Complete set 1 of Versailles T-DNA Tagged pools of 20 lines View set contents
N5389 Complete set 1 of Versailles T-DNA Tagged pools of 100 lines View set contents
N5444 Complete set 2 of Versailles T-DNA Tagged pools of 20 lines View set contents
N5455 Complete set 2 of Versailles T-DNA Tagged pools of 100 lines View set contents
N5599 Complete set 3 of Versailles T-DNA Tagged pools of 20 lines View set contents
N5600 Complete set 3 of Versailles T-DNA Tagged pools of 100 lines View set contents
N5865 Complete set 4 of Versailles T-DNA Tagged pools of 20 lines View set contents
N5866 Complete set 4 of Versailles T-DNA Tagged pools of 100 lines View set contents
N55046 Complete set 5 of Versailles T-DNA Tagged pools of 20 lines View set contents
N55047 Complete set 5 of Versailles T-DNA Tagged pools of 100 lines View set contents


The deposited 148 bulks corresponding to 1480 lines came from a collection initiated in 1992 by the discovery of a new transformation method by vacuum infiltration (Bechtold et al.1993). In 3 years we selected 16 000 independent transformants and screened 6,000 of them in vitro and in the greenhouse for mutations affecting hypocotyl elongation or gametogenesis and for flower specific promoter trapping.

Transformation method

For the in planta transformation method by vacuum infiltration we used the Arabidopsis ecotype Wassilevskija and the binary vector pGKB5, constructed by D. Bouchez (Bouchez et al. 1993). This vector contains a promoterless GUS reporter gene fused to the right border, and the genes conferring kanamycin and Basta resistance as plant selection markers

Four-week old plants, well developed, with the first fruits formed and secondary inflorescences appearing, were infiltrated for 20 minutes with an Agrobacterium culture (OD600nm= 0.8) resuspended in one-third of the initial volume in infiltration medium. Plants were then transferred to soil and 4 weeks later the seeds were harvested. The T1 transformants were then selected on sand sub-irrigated with water containing Basta (5-10 mg/l phosphinothricin), transferred to soil, and grown in plastic tubes to prevent seed contamination. The T2 seeds were harvested 6 weeks later.


A new plant transformation vector (see Figure 1 below) was designed, that could be used for T-DNA tagging in Arabidopsis. The T-DNA region of this plasmid is flanked by fragments containing the right and left borders of the TR-DNA of pRiA4 (Jouanin et al. 1989). The GUS-nos3' reporter cassette from pBI101.1 (Jefferson et al. 1987) is inserted 40 bp away from the right border. As the GUS gene possesses its own ATG initiation codon, it is able to produce active transcriptional or translational gene fusions upon its insertion in the genome. The T-DNA also contains two plant selection markers derived from pGSFR280 (De Blok et al. 1987) that confer resistance of plant cells to kanamycin and to the herbicide Basta (phosphinothricin).

This binary plasmid derives from a pBGS plasmid (Spratt et al. 1986), harbours a bacterial kanamycin resistance gene, and is able to replicate both in Escherichia coli and in Agrobacterium. The origin of replication of pRiA4, cloned as a large 8 kb BamHI fragment from pLJbB11 (Jouanin et al. 1985), confers a very high stability in Agrobacterium under non selective conditions : Agrobacterium strains containing pGKB5 show no detectable loss of the plasmid after 25 generations in medium lacking kanamycin. The binary vector was introduced into several Agrobacterium disarmed strains by electroporation : C58C1 (pMP90) (Koncz and Schell 1986), C58C1 (pGV2260) (Deblaere et al. 1985), LBA4404 (Hoekema et al. 1983) to give respectively the strains MP5-1, GV5-2, LB5-1. Strain MP5-1 was used for obtaining all the T-DNA lines generated in this collection.

Figure 1. Functional map of the binary vector pGKB5.

Arrows indicate coding sequences, and black boxes promoter / terminator regions. The right and left border fragments derived from the TR-DNA of pRiA4 from Agrobacterium rhizogenes strain A4 3 ; the black strips correspond to the 24 bp border sequences that serve as signals for T-DNA transfer. The chimeric kanamycin and Basta resistance genes originate from pGSFR280 (De Blok et al (1987). Sites for EcoRV are indicated above the T-DNA. The hatched area corresponds to the probe used in hybridization experiments. A large origin of replication from pRiA4 (ori pRiA4) (Jouanin et al 1985)has been used to insure a good stability of the vector in Agrobacterium even without selection pressure. uidA : coding region of the beta-glucuronidase from E. coli ; nos 3' : 3' region of the nopaline synthase gene from pTiC58 ; ocs 3' : 3' region of the octopine synthase gene from pTiAch5 ; nptII : neomycin phosphotransferase II ; P nos : promoter region of the nopaline synthase gene ; P 35S : promoter of the 35S transcript of the Cauliflower Mosaic Virus ; bar : coding sequence of the basta resistance gene from Streptomyces hygroscopus ; 3' g7 : 3' region of the gene 7 from the T-DNA of pTi15955.

Mutation screening

The T2 families for which enough seed was produced, were screened in vitro on medium as described by (Estelle and Somerville 1987) and modified according to (Santoni et al. 1994). About 100 seeds were sowed on medium containing 100 mg/l kanamycin to estimate the number of T-DNA insertions and screen for gametophytic mutations. The screening of the hypocotyl development mutations was carried out without selection in light and darkness 10 days after sowing. About 50 seeds of each T2 families were also sowed on compost without selection in the greenhouse to screen early development and gametogenesis mutations.

GUS screening

The GUS activity of 2,000 first T2 lines was tested histochemically on 15- days-old seedlings grown in vitro either under light or dark conditions (Mollier et al. 1995). For all the families we tested the GUS activity on flowers and siliques taken from 6 weeks old plants grown in the greenhouse.

Seed production

Because of the low number of T2 seeds it was necessary to multiply them and send the T3 generation to the Nottingham Arabidopsis Stock Centre. T3 seeds come from the bulk of about 50 T2 plants for each family. Seeds were stored at 4C and 15 % RH. The aliquots contain hemizygous, homozygous and wild type seeds.

Available data

The available data were recorded through analysis of T2 seedlings in vitro and flowering plants in the greenhouse. This information includes:

  • in vitro segregation on about 100 seeds sowed on kanamycin 100 mg/l (corresponding to 3:1 segregation, 15:1, 63:1, 2:1, ?= number of resistant plants 3.86 for all the possible segregations).
  • GUS expression at seedling stage in vitro for a limited number of lines 3.
  • GUS expression in flowers and siliques in the greenhouse.
  • seedling observations in vitro
  • plant observations in the greenhouse.

Unavailable lines

A number of lines are not yet available through NASC because we or our collaborators were interested in:

  • 1:1 segregation for kanamycin resistance.
  • lines containing about 1/4 sterile or partial sterile mutants.
  • hypocotyl development mutants.
  • leaf morphology mutants.
  • leaf necrosis mutants.
  • germination mutants.
  • yellow-green mutants.
  • specific GUS expression in flower and siliques.
  • some specific GUS expression in leaves.
  • lines we didn't test in vitro because they yielded only a few T2 seeds (1/3 of the lines, but they will be tested in T3 generation).

Restriction for the use of the Versailles-INRA T-DNA lines

These lines are freely distributed by the NASC for fundamental research purposes. Commercial application of the information obtained from the study of these lines is not possible without prior agreement with INRA.

Important notes

  • The segregation of the kanamycin marker was estimated on about 100 seedlings. This is not always enough to distinguish between segregations like 2:1 and 3:1 for example. It is then necessary to verify the segregation with more seeds (about 300).
  • For several lines no resistant progeny were recovered on kanamycin, but in Southern analysis some of them do contain the T-DNA. We decided to send all the lines even if all the plants were kanamycin sensitive. These lines were noted "?" in the segregation data.
  • We also have observed differences between GUS expression at seedling stage in vitro and in the greenhouse, and some unrepeatable GUS expression in flowers and siliques (GUS expression varied with greenhouse conditions).
  • Not all the GUS expression observed was necessarily tissue-specific. We just tested the specificity of GUS expression in the flowers and siliques.
  • The lines were not always grown and harvested in the same climatic conditions, and it is possible that this lead to some differences in the germination rate.
  • In this collection, we observed that 56 % of T-DNA integration are at a single locus, and by Southern 75 % of them are in tandem (Bechtold et al. 1993).
  • From the first studies of mutants provided by this collection, it seems that about 1/4 of the lines showing a segregation of mutants/ wild type near to 1:3 will be tagged. As already described by Feldmann, the in planta methods also appear to have a mutagenic effect.

Related links


  • Bechtold, N., Ellis, J. & Pelletier, G. 1993. In planta Agrobacterium mediated gene transfer by infiltration of adult Arabidopsis thaliana plants. C. R. Acad. Sci. Paris, Sciences de la vie/Life Sciences 316:1194-9.
  • Mollier, P. et al. 1995. Promoterless gusA expression in a large number of Arabidopsis thaliana transformants obtained by the in planta infiltration method. C.R.Acad.Sci. Paris, Sciences de la vie/Life sciences 318(4):465-74. Link to Article.