Identification and expression of cytokinin signaling and meristem identity genes in sulfur deficient grapevine (Vitis vinifera L.)

Plant Signaling and Behavior

Volumn 4, Issue 12, 2009, Pages 1128-1135

  Fernandes, João ^a   Tavares, Sílvia ^a   Amâncio, Sara ^a  

^a INSTITUTO SUPERIOR DE AGRONOMIA   (Portugal)

Author keywords

Apical meristem genes; Axillary meristem genes; Cytokinin signaling genes; Sulfur; Vitis

Indexed keywords

ARABIDOPSIS; VITACEAE; VITIS; VITIS VINIFERA; ZEA MAYS;

CYTOKININ; SULFUR;

ARTICLE; GENE EXPRESSION REGULATION; GENETICS; GRAPE; GROWTH, DEVELOPMENT AND AGING; MERISTEM; METABOLISM; PHYLOGENY; SIGNAL TRANSDUCTION;

CYTOKININS; GENE EXPRESSION REGULATION, PLANT; MERISTEM; PHYLOGENY; SIGNAL TRANSDUCTION; SULFUR; VITIS;

EID: 70849126416     PISSN: 15592316     EISSN: 15592324     Source Type: Journal    
DOI: 10.4161/psb.4.12.9942     Document Type: Article

References (57)

1. Heyl A, Schmülling T. Cytokinin signal and transduction. Curr Opin Plant Biol 2003; 6:480-8.
2. Hwang I, Sheen J. Two-component circuitry in Arabidopsis cytokinin signal transduction. Nature 2001; 413:383-9.
3. Müller B, Sheen J. Advances in cytokinin signaling. Science 2007; 318:68-9.
4. Yonekura-Sakakibara K, Kojima M, Yamaya T, Sakakibara H. Molecular characterization of cytokinin-responsive Histidine Kinases in maize. Differential ligand preferences and response to cis-Zeatin. Plant Physiol 2004; 134:1-8.
5. Ito Y, Kurata N. Identification and characterization of cytokinin-signaling gene families in rice. Gene 2006; 382:57-65.
6. West AH, Stock AM. Histidine Kinases and response regulator proteins in two-component signaling systems. Trends Biochem Sci 2001; 26:369-76.
7. Ueguchi C, Koizumi H, Suzuki T, Mizuno T. Novel family of sensor histidine kinase genes in Arabidopsis thaliana. Plant Cell Physiol 2001; 42:231-5.
8. Du L, Jiao F, Chu J, Jin G, Chen M, Wu P. The two-component signal system in rice (Oryza sativa L.): A genome-wide study of cytokinin signal perception and transduction. Genomics 2007; 89:697-707.
9. Higuchi MH, Pischke M, Mähönen A, Miyawaki K, Hashimato Y, Seki M, et al. In plant functions of Arabidopsis cytokinin receptor family. Proc Natl Acad Sci USA 2004; 101:8821-6.
10. Tanaka Y, Suzuki T, Yamashino T, Mizuno T. Comparative studies of the AHP histidine-containing phosphotransmitters implicated in His-to-Asp phosphorelay in Arabodopsis thaliana. Biosci Biotech Biochem 2004; 68:462-5.
11. Sakai H, Honma T, Aoyama T, Sato S, Kato T, Tabata S, Oka A. ARR1, a transcription factor for genes immediately responsive to cytokinin. Science 2001; 294:1519-22.
12. D' Agostino IB, Deruère J, Kieber JJ. Characterization of the response of the Arabidopsis response regulator gene family to cytokinin. Plant Physiol 2000; 124:1706-17.
13. Smith FW, Ealing PM, Hawkesford MJ, Clarkson DT. Plant members of a family of sulfate transporters reveal functional subtypes. Proc Natl Acad Sci USA 1995; 92:9373-7.
14. Smith FW, Hawkesford MJ, Ealing PM, Clarkson DT, van den Berg PJ, Belcher AR, Warrilow AGS. Regulation of expression of a cDNA from barley roots enconding a high affinity sulfate transporter. Plant J 1997; 12:875-84.
15. Takahashi H, Yamazak M, Sasakura N, Watanabe A, Leustek T, de Almeida-Engler J, et al. Regulation of sulfur in higher plants: a sulfate transporter induced in sulfate starved roots plays a central role in Arabidopsis thaliana. Proc Natl Acad Sci USA 1997; 94:11102-7.
16. Yoshimoto N, Takahashi H, Smith FW, Yamaya T, Saito K. Two distinct high-affinity sulfate transporter with different inducibilities mediate uptake of sulfate in Arabidopsis roots. Plant J 2002; 29:465-73.
17. Tavares S, Sousa C, Carvalho LC, Amâncio S. De-repressed transporters are strongly repressed after sulfate addition to sulfur depleted Vitis cells. Int J Plant Sci 2008; 169:987-97.
18. Maruyama-Nakashita A, Nakamura Y, Yamaya T, Takahashi H. A novel regulatory pathway of sulfate uptake in Arabidopsis roots: implication of CRE1/WOL/AHK4-mediated cytokinin-dependent regulation. Plant J 2004; 38:779-89.
19. Ohkama N, Takei K, Sakakibara H, Hayashi H, Yoneyama T, Fujiwara T. Regulation of sulfur-responsive gene expression by exogenously applied cytokinin in Arabidopsis thaliana. Plant Cell Physiol 2002: 43:1493-501.
20. Martín A, del Pozo J, Iglesias J, Rubio V, Solano R, de la Peña A, et al. Influence of cytokinins on the expression of phosphate starvation responsive genes in Arabidopsis. Plant J 2000; 24:559-67.
21. Franco-Zorrilla JM, Marín AC, Solano R, Rubio V, Leyva A, Paz-Ares J. Mutations at CRE1 impair cytokinin-induced repression of phosphate starvation responses in Arabidopsis. Plant J 2002; 32:353-60.
22. Sachs T, Thimann KV. Release of Lateral Buds from Apical Dominance. Nature 1964; 201:939-40.
23. Cline M, Wessel T, Iwamura HP. Cytokinin/auxin control of apical dominance in Ipomoea nil. Plant Cell Physiol 1997; 38:659-67.
24. Lenhard M, Laux T. Shoot meristem formation and maintenance. Curr Opin Plant Biol 1999; 2:44-50.
25. Bowman JL, Eshed Y. Formation and maintenance of the shoot apical meristem. Trends Plant Sci 2000; 5:110-5.
26. Uchida N, Townsley B, Chung K-H, Sinha N. Regulation of SHOOT MERISTEMLESS genes via an upstream-conserved noncoding sequence coordinates leaf development. Proc Natl Acad Sci USA 2007; 104:15953-8.
27. Long JA, Moan EI, Medford JI, Barton MK. A member of the KNOTTED class of homeodomain proteins encoded by the STM gene of Arabidopsis. Nature 1996; 379:66-9.
28. Mar Castellano M, Sablowski R. Intercellular signaling in the transition from stem cells to organogenesis in meristems. Curr Opin Plant Biol 2005; 8:26-31.
29. Fletcher JC, Brand U, Running MP, Simon R, Meyerowitz EM. Signaling of cell fate decisions by CLAVATA3 in Arabidopsis shoot meristems. Science 1999; 283:1911-4.
30. Lenhard M, Jurgens G, Laux T. The WUSCHEL and SHOOTMERISTEMLESS genes fulfil complementary roles in Arabidopsis shoot meristem regulation. Development 2002; 129:3195-206.
31. Brand U, Fletcher JC, Hobe M, Meyerowitz EM, Simon R. Dependence of stem cell fate in Arabidipsis on feedback loop regulation by CLV3 activity. Science 2000; 289:617-9.
32. Ongaro V, Leyser O. Hormonal control of shoot branching. J Exp Bot 2008; 59:67-74.
33. Greb T, Clarenz O, Schäfer, E, Müller, D, Herrero R, Schmitz G, Theres K. Molecular analysis of the LATERAL SUPRESSOR genes in Arabidopsis reveals a conserved control mechanism for axillary meristem formation. Genes Dev 2003; 17:1175-87.
34. Keller T, Abbott J, Moritz T, Doerner P. Arabidopsis REGULATOR OF AXILLARY MERISTEMS1 controls a leaf axil stem cell niche and modulates vegetative development. Plant Cell 2006; 18:598-611.
35. Muller D, Schmitz G, Theres K. Blind homologous R2R3 Myb genes control the pattern of lateral meristem initiation in Arabidopsis. Plant Cell 2006; 18:586-97.
36. Doebley J, Stec A, Hubbard L. The evolution of apical dominance in maize. Nature 1997; 386:485-8.
37. Hu W, Zhang S, Zhao Z, Sun C, Zhao Y, Luo D. The analysis of the structure and expression of Os TB1 gene in rice. J Plant Physiol Mol Biol 2003; 29:507-14.
38. Takeda T, Suwa Y, Suzuki M, Kitano H, Ueguchi-Tanaka M, Ashikari M, et al. The Os TB1 gene negatively regulates lateral branching in rice. Plant J 2003; 33:513-20.
39. Hubbard L, McSteen P, Doebley J, Hake S. Expression patterns and mutant phenotype of teosinte branched1 correlate with growth suppression in maize and teosinte. Genetics 2002; 162:1927-35.
40. Otsuga D, DeGuzman B, Prigge M, Drews GN, Clark S. REVOLUTA regulates meristem initiation at lateral positions. Plant J 2001; 25:223-36.
41. Aguilar-Martínez J, Poza-Carrión C, Cubas P. Arabidopsis BRANCHED1 acts as an integrator of branching signals within axillary buds. Plant Cell 2007; 19:458-72.
42. Jaillon O, Aury JO, Noel B, et al. The grapevine genome sequence suggests ancestral hexaploidization in major angiosperm phyla. Nature 2007; 449:463-7.
43. Velasco R, Zharkikh A, Troggio M, Cartwright DA, Cestaro A, et al. A high quality draft consensus sequence of the genome of a heterozygous grapevine variety. PLoS ONE 2007; 2:1326.
44. Beemster GTS, Baskin TI. STUNTED PLANT 1 mediates effects of cytokinin, but not of auxin, on cell division and expansion in the root of Arabidopsis. Plant Physiol 2000; 124:1718-27.
45. Heyl A, Werner T, Schmülling T. Cytokinin metabolism and signal transduction. In Hedden P, Thomas SG, eds. Plant Hormone Signaling. Oxford, UK: Blackwell Publ Ltd 2006; 93-123.
46. Gachon C, Mingam A, Charrier B. Real-time PCR: what relevance to plant studies? J Exp Bot 2004; 55:1445-54.
47. Kiba T, Taniguchi M, Imamura A, Ueguchi C, Mizuno T, Sugiyama T. Differential expression of genes for response regulators in response to cytokinins and nitrate in Arabidopsis thaliana. Plant Cell Physiol 1999; 40:767-71.
48. Amtmann A, Armengaud P. Effects of N, P, K and S on metabolism: new knowledge gained from multi-level analysis. Curr Opin Plant Biol 2009; 12:275-83.
49. Barton MK, Poethig RS. Formation of the shoot apical meritem in Arabidopsis thaliana: an analysis in the wild type and in the shoot meristemless mutant. Development 1993; 119:823-31.
50. Bolle C. The role of GRAS proteins in plant signal transduction and development. Planta 2004; 218:683-92.
51. Jackson P, Galinha C, Pereira C, Fortunato A, Soares N, Amâncio S, Pinto Ricardo C. Rapid deposition of extensin during the elicitation of grapevine callus cultures is specifically catalysed by a 40 kDa peroxidase. Plant Physiol 2001; 127:1065-76.
52. Murashige T, Skoog F. A revised medium for rapid growth and bioassays with tobacco tissue. Physiol Plant 1962; 15:493-7.
53. 2 by tissue printing as a precocious marker of rhizogenesis in grapevine. Plant Physiol Biochem 1998; 36:817-24.
54. Godoy-Hernández G, Vázquez F. Growth measurements: estimation of cell division and cell expansion. In: Loyola-Vargas V, Vázquez-Flota F, ed. Plant cell culture protocols. U.S.: Humana Press INC 2005; 51-8.
55. rd 2009).
56. Reid KE, Olsson N, Schlosser J, Peng F, Lund ST. An optimized grapevine RNA isolation procedure and statistical determination of reference genes for real-time RT-PCR during berry development. BMC Plant Biol 2006; 6:27.
57. Bovy A, de Vos R, Kemper M, Schijlen E, Pertejo MA, Muir S, et al. High-Flavonol tomatoes resulting from the heterologous expression of the maize transcription factor genes LC and C1. Plant Cell 2002; 14:2509-26.