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@PHDTHESIS{Kruse:56523,
      author       = {Kruse, Cordula Maria},
      othercontributors = {Slusarenko, Alan},
      title        = {{C}harakterisierung des {GR}1-{G}ens aus {A}rabidopsis
                      thaliana ({L}.) {H}eynh. im {H}inblick auf die
                      rassenspezifische {R}esistenz des Ökotypen {W}assilewskija
                      gegenüber dem {P}eronospora parasitica-{I}solat {WELA}},
      address      = {Aachen},
      publisher    = {Publikationsserver der RWTH Aachen University},
      reportid     = {RWTH-CONV-118618},
      pages        = {143 S. : Ill., graph. Darst.},
      year         = {2001},
      note         = {Retraction. Aus rechtlichen Gründen kann der Zugriff nicht
                      gewährt werden.; Aachen, Techn. Hochsch., Diss., 2001},
      abstract     = {In this study the role of the GR1 gene in the race-specific
                      resistance of the Arabidopsis ecotype Ws to the P.
                      parasitica isolate WELA was investigated. In the susceptible
                      gr1 mutant GR1 is tagged by a T-DNA insert and it was
                      important to establish whether the mutant phenotype was
                      indeed due to the T-DNA insertion in GR1. Therefore, gr1
                      plants were retransformed using different genomic
                      constructs. Independent transformant lines showed local
                      resistance responses after inoculation with WELA and these
                      were not apparent in control plants. However, a completely
                      resistant transformant was not observed. An 8 kb genomic
                      fragment containing the GR1 gene was sequenced. The
                      predicted GR1 protein has a $57\%$ similarity to the ILR1
                      protein (Bartel und Fink, 1995), but not the same enzyme
                      activity. GR1 transcripts accumulated in leaves after
                      inoculation with WELA, wounding or treatment with
                      methyljasmonate. However, transcripts did not accumulate
                      after exposure to extreme temperatures, infection with P.
                      syringae pv. maculicola, or application of salicylic acid.
                      It was shown that the GR1 protein interacts with 14-3-3
                      proteins in a yeast-two-hybrid-assay, suggesting a potential
                      mechanism for GR1-mediated signal transmission. The analysis
                      of the GR1 gene and its product will lead to the
                      identification of further components of signal pathways
                      important in disease resistance and improve our
                      understanding of race-specific signal transduction in plant
                      defence.},
      cin          = {100000},
      ddc          = {570},
      cid          = {$I:(DE-82)100000_20140620$},
      typ          = {PUB:(DE-HGF)11},
      urn          = {urn:nbn:de:hbz:82-opus-1640},
      doi          = {10.18154/RWTH-CONV-118618},
      url          = {https://publications.rwth-aachen.de/record/56523},
}