Klaus Apel

Klaus Apel

Scientist

Office/Lab: Room 305

Contact:kha24@cornell.edu / 607-279-7734

Affiliations:

Graduate Field: Plant Biology, Plant Genetics

Klaus Apel

Research Summary

One of the first reactions of plants under stress is the enhanced production of chemically distinct reactive oxygen species (ROS). A major difficulty in elucidating the biological activity of ROS during stress stems from the fact that not only one but several chemically distinct ROS are generated simultaneously, thus making it very difficult to link a particular stress response to a specific ROS. This problem has been alleviated by using the conditional flu mutant of Arabidopsis that allows to induce the production of only one ROS, singlet oxygen, within plastids in a non-invasive, controlled manner (Fig. 1). In the dark the flu mutant accumulates protochlorophyllide (Pchlide), a potent photosensitizer that upon illumination generates singlet oxygen. Several singlet oxygen-mediated stress responses have been distinguished during re-illumination of the flu mutant. Inactivation of nuclear genes encoding the two closely related plastid proteins Executer1 and Executer2 has been shown to be sufficient to abrogate these stress responses despite the ongoing release of singlet oxygen. By varying the length of the dark period, one can adjust the level of the photosensitizer Pchlide and define conditions that minimize the cytotoxicity of singlet oxygen and either endorse acclimation in flu plants exposed to a very short dark period as one extreme or promote a genetically controlled cell death response in plants shifted for a longer period to the dark as another extreme (Fig. 2). This activity of singlet oxygen assigns a new function to the chloroplast, namely that of a sensor of environmental changes that activates a broad range of stress responses, known to be activated also by abiotic and biotic stressors. Our work is aimed at dissecting the complexity of singlet oxygen signalling and understanding and eventually also modifying the genetic constraints that determine the adaptability of plants to environmental changes.

Klaus Apel
Figure 1

Figure 1 FLU-dependent control of light-dependent Chl biosynthesis. Inactivation of FLU impedes negative feedback control (A) and leads to the overaccumulation of excess Pchlide in etiolated flu seedlings that upon excitation with blue light emits a strong red fluorescence (B, DD). Upon light exposure Pchlide acts as a photosensitizer and triggers the release of 1O2 that results in the rapid bleaching of seedlings (B, DL). Under continuous light Pchlide is immediately reduced via POR to Chlide and does not reach critical levels that may evoke the production of 1O2 (B, LL).

Klaus Apel
Figure 2

Figure 2 Schematic diagram of 1O2-dependent signal transduction from the plastid to the nucleus that triggers stress responses ranging from acclimation to cell death. The quality of the response can be modulated by shifting flu plants for various lengths of time to the dark, by activating modulators (e.g. PRL1) or by inactivating EX1 and/or EX2.

Publications

  • Kim C, Lee KP, Baruah A, Nater M, Göbel C, Feussner I, Apel K. 2009. 1O2-mediated retrograde signaling during late embryogenesis predetermines plastid differentiation in seedlings by recruiting abscisic acid. Proc Natl Acad Sci U S A. : May 29. [Epub ahead of print]
  • Baruah A, Simková K, Apel K, Laloi C. 2009. Arabidopsis mutants reveal multiple singlet oxygen signaling pathways involved in stress response and development. Plant Mol Biol : 2009 May 17. [Epub ahead of print]
  • Coll NS, Danon A, Meurer J, Cho WK, Apel K. 2009. Characterization of soldat8, a suppressor of singlet oxygen-induced cell death in Arabidopsis seedlings. Plant Cell Physiol Apr Epub 2009 Mar 8 5(4): 707-18
  • Przybyla, D., Göbel, C., Imboden, A., Feussner, I., Hamberg, M. and Apel, K. 2008. Enzymatic, but not non-enzymatic (1)O(2)-mediated peroxidation of polyunsaturated fatty acids forms part of the EXECUTER1-dependent stress response program in the flu mutant of Arabidopsis thaliana. Plant J. 54: 236-48
  • Kim, C., Meskauskiene, R., Apel, K., and Laloi, C. 2008. No single way to understand singlet oxygen signalling in plants. EMBO Rep 5: 435-9
  • Laloi, C, Stachowiak, M., Pers-Kamczyc, E., Warzych, E., Murgia, I., and Apel, K. 2007. Cross-talk between singlet oxygen- and hydrogen peroxide-dependent signaling of stress responses in Arabidopsis thaliana. Proc Natl Acad Sci U S A 104: 672-7
  • Lee, K.P., Kim, C., Landgraf, F., Apel, K. 2007. EXECUTER1- and EXECUTER2-dependent transfer of stress-related signals from the plastid to the nucleus of Arabidopsis thaliana. Proc Natl Acad Sci U S A 104: 10270-5
  • Laloi, C., Przybyla, D., and Apel, K. 2006. A genetic approach towards elucidating the biological activity of different reactive oxygen species in Arabidopsis thaliana. J Exp Bot 57: 1719-24. Review.
  • Laloi, C., Apel, K. and Danon, A. 2004. Reactive oxygen signalling: the latest news. Curr. Opin. Plant Biol 7: 323-8
  • op den Camp, R.G., Przybyla, D., Ochsenbein, C., Laloi, C., Kim, C., Danon, A., Wagner, D., Hideg, E., Göbel, C., Feussner, I., Nater, M. and Apel, K. 2003. “Rapid induction of distinct stress responses after the release of singlet oxygen in Arabidopsis.”. Plant Cell 15: 2320-2332

Lab Members

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Lab Member
Chanhong Kim
Lab Member
Aiswarya Baruah
Lab Member
Zhipan Yang