cGMP in ozone and NO dependent responses

We have recently reported (Plant Physiology 2006; 142:595-608) that ozone (O3) can inhibit mitochondrial respiration and induce activation of the alternative oxidase (AOX) pathway and in particular AOX1a in tobacco. While O3 causes mitochondrial H2O2, early leaf nitric oxide (NO) as well as transient ethylene (ET) accumulation, the levels of jasmonic acid and 12-oxo-phytodienoic acid remained unchanged. It was shown that both, NO and ET dependent pathways can induce AOX1a transcription by O3. AOX plays a role in reducing reactive oxygen species (ROS) which in turn are linked to biotic and abiotic plant stresses, much like the second messengers guanosine 3’, 5’-cyclic monophosphate (cGMP). The goal is to unravel specific cGMP signatures and induction pathways downstream from O3 and NO, including transcription of AOX1a. Here we propose that some late (> 3 hours) responses to NO, e.g. the accumulation of phenylalanine lyase (PAL) transcripts, are critically cGMP dependent, while the early (< 2 hours) responses, including AOX1a induction are not.

[1]  M. Delledonne NO news is good news for plants. , 2005, Current opinion in plant biology.

[2]  J. Durner,et al.  Nitric oxide induces transcriptional activation of the nitric oxide-tolerant alternative oxidase in Arabidopsis suspension cells , 2002, Planta.

[3]  H. Lambers,et al.  Enhanced expression and activation of the alternative oxidase during infection of Arabidopsis with Pseudomonas syringae pv tomato. , 1999, Plant physiology.

[4]  C. Wasternack,et al.  Interaction between Nitric Oxide and Ethylene in the Induction of Alternative Oxidase in Ozone-Treated Tobacco Plants1[W] , 2006, Plant Physiology.

[5]  Erwin Witters,et al.  Tansley Review No. 106: Cyclic nucleotides in higher plants: the enduring paradox. , 1999, The New phytologist.

[6]  R. Shewfelt,et al.  Does the alternative pathway ameliorate chilling injury in sensitive plant tissues? , 1993, Physiologia plantarum.

[7]  L. Reale,et al.  Ozone-Induced Cell Death in Tobacco Cultivar Bel W3 Plants. The Role of Programmed Cell Death in Lesion Formation , 2003, Plant Physiology.

[8]  J. Hancock,et al.  Nitric oxide signalling in plants. , 2003, The New phytologist.

[9]  K. Denby,et al.  Salt and osmotic stress cause rapid increases in Arabidopsis thaliana cGMP levels , 2004, FEBS letters.

[10]  L. Mcintosh,et al.  Mitochondrial Electron Transport Regulation of Nuclear Gene Expression (Studies with the Alternative Oxidase Gene of Tobacco) , 1994, Plant physiology.

[11]  L. Reale,et al.  Salicylic acid modulates ozone-induced hypersensitive cell death in tobacco plants. , 2002, Physiologia plantarum.

[12]  D. Klessig,et al.  Defense gene induction in tobacco by nitric oxide, cyclic GMP, and cyclic ADP-ribose. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[13]  D Marshall Porterfield,et al.  Nitric oxide is involved in growth regulation and re-orientation of pollen tubes , 2004, Development.

[14]  L. Mcintosh,et al.  Cytochrome and Alternative Pathway Respiration in Tobacco (Effects of Salicylic Acid) , 1993, Plant physiology.

[15]  F. Maathuis cGMP modulates gene transcription and cation transport in Arabidopsis roots. , 2006, The Plant journal : for cell and molecular biology.

[16]  K. Krab,et al.  The alternative respiration pathway in plants : role and regulation , 1995 .

[17]  P. Schaap Guanylyl cyclases across the tree of life. , 2005, Frontiers in bioscience : a journal and virtual library.

[18]  F. Paolocci,et al.  The overexpression of an alternative oxidase gene triggers ozone sensitivity in tobacco plants. , 2007, Plant, cell & environment.

[19]  F. Paolocci,et al.  Gene expression profiles of O3-treated Arabidopsis plants. , 2006, Plant, cell & environment.

[20]  C. Gehring,et al.  Emerging roles in plant biotechnology for the second messenger cGMP - guanosine 3', 5'-cyclic monophosphate , 2006 .