Conserved functions of arabidopsis and rice CC-type glutaredoxins in flower development and pathogen response

Molecular Plant

Volumn 2, Issue 2, 2009, Pages 323-335

  Wang, Zhen ^a,b   Xing, Shuping ^a,c   Birkenbihl, Rainer P ^a   Zachgo, Sabine ^a,c  

^a MAX PLANCK INSTITUTE FOR PLANT BREEDING RESEARCH   (Germany)

^b UNIVERSITY OF NEBRASKA   (United States)

^c UNIVERSITY OF OSNABRÜCK   (Germany)

Author keywords

Arabidopsis; Botrytis cinerea; Flower development; Glutaredoxin; Pathogen defence; Rice; ROXY1

Indexed keywords

ARABIDOPSIS; BOTRYOTINIA FUCKELIANA; EMBRYOPHYTA; LILIOPSIDA;

GLUTAREDOXIN;

AMINO ACID SEQUENCE; ARABIDOPSIS; CHEMISTRY; CONSERVED SEQUENCE; FLOWER; GROWTH, DEVELOPMENT AND AGING; IN SITU HYBRIDIZATION; METABOLISM; MICROBIOLOGY; MOLECULAR GENETICS; ORYZA; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SEQUENCE HOMOLOGY;

AMINO ACID SEQUENCE; ARABIDOPSIS; CONSERVED SEQUENCE; FLOWERS; GLUTAREDOXINS; IN SITU HYBRIDIZATION; MOLECULAR SEQUENCE DATA; ORYZA; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SEQUENCE HOMOLOGY, AMINO ACID;

EID: 65249163613     PISSN: 16742052     EISSN: 17529867     Source Type: Journal    
DOI: 10.1093/mp/ssn078     Document Type: Article

References (41)

1. Ambrose, B.A., Lerner, D.R., Ciceri, P., Padilla, C.M., Yanofsky, M.F., and Schmidt, R.J. (2000). Molecular and genetic analyses of the silkyl gene reveal conservation in floral organ specification between eudicots and monocots. Mol. Cell. 5, 569-579.
2. Asselbergh, B., Curvers, K., Franca, S.C., Audenaert, K., Vuylsteke, M., Van Breusegem, F., and Höfte, M. (2007). Resistance to Botrytis cinerea in sitiens, an abscisic acid-deficient tomato mutant, involves timely production of hydrogen peroxide and cell wall modifications in the epidermis. Plant Physiol. 144, 1863-1877.
3. Aziz, A., Heyraud, A., and Lambert, B. (2004). Oligogalacturonide signal transduction, induction of defense-related responses and protection of grapevine against Botrytiscinerea. Planta. 218, 767-774.
4. Bandyopadhyay, S., et al. (2008). Chloroplast monothiol glutare-doxins as scaffold proteins for the assembly and delivery of [2Fe-2S] clusters. EMBO J. 27, 1122-1133.
5. Bommert, P., Satoh-Nagasawa, N., Jackson, D., and Hirano, H.Y. (2005). Genetics and evolution of inflorescence and flower development in grasses. Plant Cell Physiol. 46, 69-78.
6. Buchanan, B.B., and Balmer, Y. (2005). Redox regulation: a broadening horizon. Annu. Rev. Plant Biol. 56, 187-220.
7. Cheng, N.H. (2008). AtGRX4, an Arabidopsis chloroplastic monothiol glutaredoxin, is able to suppress yeast grx5 mutant pheno-types and respond to oxidative stress. FEBS Lett. 582, 848-854.
8. Cheng, N.H., Liu, J.Z., Brock, A., Nelson, R.S., and Hirschi, K.D. (2006). AtGRXcp, an Arabidopsis chloroplastic glutaredoxin, is critical for protection against protein oxidative damage. J. Biol. Chem. 281, 26280-26288.
9. Elad, Y. (1997). Responses of plants to infection by Botrytis cinerea and novel means involved in reducing their susceptibility to infection. Biol. Rev. Camb. Philos. Soc. 72, 381-422.
10. Fernandes, A.P., and Holmgren, A. (2004).Glutaredoxins: glutathione-dependent redox enzymes with functions far beyond a simple thioredoxin backup system. Antioxid. Redox Signal. 6, 63-74.
11. Gallogly, M.M., and Mieyal, J.J. (2007). Mechanisms of reversible protein glutathionylation in redox signaling and oxidative stress. Curr. Opin. Pharmacol. 7, 381-391.
12. Govrin, E.M., and Levine, A. (2000). The hypersensitive response facilitates plant infection by the necrotrophic pathogen Botrytis cinerea. Curr. Biol. 10, 751-757.
13. Herrero, E., Ros, J., Bellí, G., and Cabiscol, E. (2007). Redox control and oxidative stress in yeast cells. Biochim. Biophys. Acta. doi:10.1016/j.bbagen.2007.12.004.
14. Ikeda, K., Sunohara, H., and Nagato, Y. (2004). Developmental course of inflorescence and spikelet in rice. Breed. Sci. 54, 147-156.
15. Itoh, J., Nonomura, K., Ikeda, K., Yamaki, S., Inukai, Y., Yamagishi, H., Kitano, H., and Nagato, Y. (2005). Rice plant development: from zygote to spikelet. Plant Cell Physiol. 46, 23-47.
16. Kazan, K., Murray, F.R., Goulter, K.C., Llewellyn, D.J., and Manners, J.M. (1998). Induction of cell death in transgenic plants expressing a fungal glucose oxidase. Molecular Plant-Microbe Interations. 11, 555-562.
17. Kim, B.R., Nam, H.Y., Kim, S.U., Kim, S.I., and Chang, Y.J. (2003). Normalization of reverse transcription quantitative-PCR with housekeeping genes in rice. Biotechnol. Lett. 25, 1869-1872.
18. Lemaire, S.D. (2004). The glutaredoxin family in oxygenic photosyn-thetic organisms. Photosynth. Res. 79, 305-318.
19. Luikenhuis, S., Perrone, G., Dawes, I.W., and Grant, C.M. (1998). The yeast Saccharomyces cerevisiae contains two glutaredoxin genes that are required for protection against reactive oxygen species. Mol. Biol. Cell. 9, 1081-1091.
20. Malcomber, S.T., and Kellogg, E.A. (2004). Heterogeneous expression patterns and separate roles of the SEPALLATA gene LEAFY HULL STERILE1 in grasses. Plant Cell. 16, 1692-1706.
21. Małolepsza, U., and Rózalska, S. (2005). Nitric oxide and hydrogen peroxide in tomato resistance. Nitric oxide modulates hydrogen peroxide level in o-hydroxyethylorutin-induced resistance to Botrytis cinerea in tomato. Plant Physiol. Biochem. 43, 623-635.
22. Ndamukong, I., Abdallat, A.A., Thurow, C., Fode, B., Zander, M., Weigel, R., and Gatz, C. (2007). SA-inducible Arabidopsis glutaredoxin interacts with TGA factors and suppresses JA-responsive PDF1.2 transcription. Plant J. 50, 128-139.
23. Prasad, K., Sriram, P., Kumar, C.S., Kushalappa, K., and Vijayraghavan, U. (2001). Ectopic expression of rice OsMADS1 reveals a role in specifying the lemma and palea, grass floral organs analogous to sepals. Dev. Genes Evol. 211, 281-290.
24. Rodriguez, A.A., Grunberg, K.A., and Taleisnik, E.L. (2002). Reactive oxygen species in the elongation zone of maize leaves are necessary for leaf extension. Plant Physiol. 129, 1627-1632.
25. Rouhier, N., et al. (2007). Functional, structural, and spectroscopic characterisation of a glutathione-ligated [2Fe-2S] cluster in poplar glutaredoxin C1. Proc. Natl Acad. Sci. USA. 104, 7379-7384.
26. Rouhier, N., Gelhaye, E., and Jacquot,J.P. (2004). Plant glutaredoxins: still mysterious reducing systems. Cell Mol. Life Sci. 61, 1266-1277.
27. Rouhier, N., Lemaire, S.D., and Jacquot, J.P. (2008). The role of glutathione in photosynthetic organisms: emerging functions for glutaredoxins and glutathionylation. Annu. Rev. Plant Biol. 59, 143-166.
28. Sagi, M., Davydov, O., Yesbergenova, Z., Ophir, R., Stratman, J.W., and Fluhr, R. (2004). Plant respiratory burst oxidase homologs impinge on wound responsiveness and development in Lycopersicum esculentum. Plant Cell. 16, 616-628.
29. Schmidt, R.J., and Ambrose, B.A. (1998). The blooming of grass flower development. Curr. Opin. Plant Biol. 1, 60-67.
30. Sha, S., et al. (1997). Purification and characterization of glutaredoxin (thioltransferase) from rice (Oryza sativa L.). J. Biochem. 121, 842-848.
31. Torres, M.A., Dangl, J.L., and Jones, J.D. (2002). Arabidopsis gp91phox homologues AtrbohD and AtrbohF are required for accumulation of reactive oxygen intermediates in the plant defense response. Proc. Natl Acad. Sci. USA. 99, 517-522.
32. Tsukamoto, S., Morita, S., Hirano, E., Yokoi, H., Masumura, T., and Tanaka, K. (2005). A novel cis-element that is responsive to oxidative stress regulates three antioxidant defense genes in rice. Plant Physiol. 137, 317-327.
33. Whipple, C.J., Ciceri, P., Padilla, CM., Ambrose, B.A., Bandong, S.L., and Schmidt, R.J. (2004). Conservation of B-class floral homeotic gene function between maize and Arabidopsis. Development. 131, 6083-6091.
34. Whipple, C.J., Zanis, M.J., Kellogg, E.A., and Schmidt, R.J. (2007). Conservation of B class gene expression in the second whorl of a basal grass and outgroups links the origin of lodicules and petals. Proc. Natl Acad. Sci. USA. 104, 1081-1086.
35. Wolfe, K.H., Gouy, M., Yang, Y.W., Sharp, P.M., and Li, W.H. (1989). Date of the monocot-dicot divergence estimated from chloroplast DNA sequence data. Proc. Natl Acad. Sci. USA. 86, 6201-6205.
36. van Baarlen, P., van Belkum, A., Summerbell, R.C., Crous, P.W., and Thomma, B.P. (2007). Molecular mechanisms of pathogenicity: how do pathogenic microorganisms develop cross-kingdom host jumps? FEMS Microbiol. Rev. 31, 239-277.
37. Xing, S., and Zachgo, S. (2008). ROXY1 and ROXY2, two Arabidopsis glutaredoxin genes, are required for anther development. Plant J. 53, 790-801.
38. Xing, S., Lauri, A., and Zachgo, S. (2006). Redox regulation and flower development: a novel function for glutaredoxins. Plant Biol. 8, 547-555.
39. Xing, S., Rosso, M.G., and Zachgo, S. (2005). ROXY1, a member of the plant glutaredoxin family, is required for petal development in Arabidopsis thaliana. Development. 132, 1555-1565.
40. Yadav, S.R., Prasad, K., and Vijayraghavan, U. (2007). Divergent regulatory OsMADS2 functions control size, shape and differentiation of the highly derived rice floret second-whorl organ. Genetics. 176, 283-294.
41. Zachgo, S. (2002). In situ hybridization. In Molecular Plant Biology, Gilmartin P.M. and Blower C., eds (Oxford, UK: Oxford University Press), pp. 41-63.