The Arabidopsis thaliana proteome harbors undiscovered multi-domain molecules with functional guanylyl cyclase catalytic centers

BackgroundSecond messengers link external cues to complex physiological responses. One such messenger, 3’,5’-cyclic guanosine monophosphate (cGMP), has been shown to play a key role in many physiological responses in plants. However, in higher plants, guanylyl cyclases (GCs), enzymes that generate cGMP from guanosine-5’-triphosphate (GTP) have remained elusive until recently. GC search motifs constructed from the alignment of known GCs catalytic centers form vertebrates and lower eukaryotes have led to the identification of a number of plant GCs that have been characterized in vitro and in vivo.Presentation of the hypothesisRecently characterized GCs in Arabidopsis thaliana contributed to the development of search parameters that can identify novel candidate GCs in plants. We hypothesize that there are still a substantial number (> 40) of multi-domain molecules with potentially functional GC catalytic centers in plants that remain to be discovered and characterized.Testing the hypothesisThe hypothesis can be tested, firstly, by computational methods constructing 3D models of selected GC candidates using available crystal structures as templates. Homology modeling must include substrate docking that can provide support for the structural feasibility of the GC catalytic centers in those candidates. Secondly, recombinant peptides containing the GC domain need to be tested in in vitro GC assays such as the enzyme-linked immune-sorbent assay (ELISA) and/or in mass spectrometry based cGMP assays. In addition, quantification of in vivo cGMP transients with fluorescent cGMP-reporter assays in wild-type or selected mutants will help to elucidate the biological role of novel GCs.Implications of the hypothesisIf it turns out that plants do harbor a large number of functional GC domains as part of multi-domain enzymes, then major new insights will be gained into the complex signal transduction pathways that link cGMP to fundamental processes such as ion transport and homeostasis, biotic and abiotic stress responses as well as cGMP-dependent responses to hormones.

[1]  C. Seoighe,et al.  An Increasingly Complex and Growing Family , 2007 .

[2]  C. Gehring,et al.  Ozone and nitric oxide induce cGMP-dependent and -independent transcription of defence genes in tobacco. , 2009, The New phytologist.

[3]  A. Beck‐Sickinger,et al.  Cell Communication and Signaling , 2009 .

[4]  C. Gehring,et al.  Stomatal guard cell responses to kinetin and natriuretic peptides are cGMP-dependent , 1998, Cellular and Molecular Life Sciences (CMLS).

[5]  Emmanuel Iwuoha,et al.  Identification of a novel Arabidopsis thaliana nitric oxide‐binding molecule with guanylate cyclase activity in vitro , 2011, FEBS letters.

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

[7]  G. Berkowitz,et al.  Reply to Ashton: The putative guanylyl cyclase domain of AtPepR1 and similar plant receptors , 2011, Proceedings of the National Academy of Sciences.

[8]  Tanya Z. Berardini,et al.  PatMatch: a program for finding patterns in peptide and nucleotide sequences , 2005, Nucleic Acids Res..

[9]  Arthur J. Olson,et al.  AutoDock Vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading , 2009, J. Comput. Chem..

[10]  Adam S. Dawe,et al.  Evolutionary and Structural Perspectives of Plant Cyclic Nucleotide-Gated Cation Channels , 2012, Front. Plant Sci..

[11]  Helen Irving,et al.  The Arabidopsis thaliana Brassinosteroid Receptor (AtBRI1) Contains a Domain that Functions as a Guanylyl Cyclase In Vitro , 2007, PloS one.

[12]  Chris Gehring,et al.  The Phytosulfokine (PSK) Receptor Is Capable of Guanylate Cyclase Activity and Enabling Cyclic GMP-dependent Signaling in Plants* , 2011, The Journal of Biological Chemistry.

[13]  Kathryn S Lilley,et al.  Structural and functional characteristics of cGMP-dependent methionine oxidation in Arabidopsis thaliana proteins , 2013, Cell Communication and Signaling.

[14]  A. R. Ashton Guanylyl cyclase activity in plants? , 2011, Proceedings of the National Academy of Sciences.

[15]  N. Chua,et al.  Phytochrome signal transduction pathways are regulated by reciprocal control mechanisms. , 1994, Genes & development.

[16]  R. Verma,et al.  Ca2+ signaling by plant Arabidopsis thaliana Pep peptides depends on AtPepR1, a receptor with guanylyl cyclase activity, and cGMP-activated Ca2+ channels , 2010, Proceedings of the National Academy of Sciences.

[17]  Chris Gehring,et al.  The Arabidopsis Wall Associated Kinase-Like 10 Gene Encodes a Functional Guanylyl Cyclase and Is Co-Expressed with Pathogen Defense Related Genes , 2010, PloS one.

[18]  Chris Gehring,et al.  Identification of a Novel Protein with Guanylyl Cyclase Activity in Arabidopsis thaliana * , 2003, The Journal of Biological Chemistry.

[19]  C. Gehring,et al.  Moonlighting kinases with guanylate cyclase activity can tune regulatory signal networks , 2012, Plant signaling & behavior.

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

[21]  T. Blundell,et al.  Comparative protein modelling by satisfaction of spatial restraints. , 1993, Journal of molecular biology.

[22]  N. Chua,et al.  Cyclic GMP and calcium mediate phytochrome phototransduction , 1994, Cell.

[23]  Chris Gehring,et al.  Adenyl cyclases and cAMP in plant signaling - past and present , 2010, Cell communication and signaling : CCS.

[24]  F. Maathuis,et al.  The cyclic nucleotide cGMP is involved in plant hormone signalling and alters phosphorylation of Arabidopsis thaliana root proteins , 2012, Journal of experimental botany.