Molecular Genetic Analysis of Leaf Senescence in Arabidopsis

  • Woo, Hye-Ryun (The National Research Laboratory for Plant Senescence, Division of Molecular and Life Sciences, Pohang University of Science and Technology) ;
  • Lee, Ung (The National Research Laboratory for Plant Senescence, Division of Molecular and Life Sciences, Pohang University of Science and Technology) ;
  • Cho, Sung-Whan (The National Research Laboratory for Plant Senescence, Division of Molecular and Life Sciences, Pohang University of Science and Technology) ;
  • Lim, Pyung-Ok (The National Research Laboratory for Plant Senescence, Division of Molecular and Life Sciences, Pohang University of Science and Technology) ;
  • Nam, Hong-Gil (The National Research Laboratory for Plant Senescence, Division of Molecular and Life Sciences, Pohang University of Science and Technology)
  • Published : 2000.07.01

Abstract

Senescence is a sequence of biochemical and physiological events that lead to death of a cell, organ, or whole organism. Senescence is now clearly regarded as a genetically determined and evolutionarilly acquired developmental process comprising the final stage of development. However, in spite of the biological and practical importance, genetic mechanism of senescence has been very limited. Through forward and reverse genetic approaches, we are trying to reveal the molecular and genetic mechanism of senescence in plants, employing leaf organs of Arabidopsis as a model system. Using forward genetic approach, we have initially isolated several delayed senescence mutants either from T-DNA insertional lines or chemical-mutagenized lines. In the case of ore 4 and ore 9 mutants, the mutated genes were identified. The recent progress on characterization of mutants and identification of the mutated genes will be reported. We are also screening mutations from other various sources of mutant pools, such as activation tagging lines and promoter trap lines. Two dominant senescence-delayed mutants were isolated from the activation tagging pool. Cloning of the genes responsible for this phenotype is in progress. For reverse genetic approach, the genes that induced during leaf senescence were first isolated by differential screening method. We are currently using PCR-based suppression subtractive hybridization, designed to enrich a cDNA library for rare differentially expressed transcripts. Using this method, we have identified over 35 new sequences that are upregulated at leaf senescence stage. We are investigating the function of these novel genes by systemically generating antisense lines.

Keywords

References

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