Floral reversion mechanism in longan (Dimocarpus longan Lour.) revealed by proteomic and anatomic analyses

Journal of Proteomics

Volumn 75, Issue 4, 2012, Pages 1099-1118

  You, Xiangrong ^a,b   Wang, Lingxia ^a   Liang, Wenyu ^a,c   Gai, Yonghong ^a   Wang, Xiaoyan ^a   Chen, Wei ^a  

^a FUJIAN AGRICULTURE AND FORESTRY UNIVERSITY   (China)

^b NATIONAL ENGINEERING RESEARCH CENTER FOR NON FOOD BIOREFINERY   (China)

^c NINGXIA UNIVERSITY   (China)

Author keywords

2 DE; D. longan; Differential proteins; Flowering reversion; Ultrastructure

Indexed keywords

ABC TRANSPORTER; ACONITATE HYDRATASE; ADENOSINE TRIPHOSPHATE DEPENDENT PROTEINASE; ALPHA TUBULIN; BETA TUBULIN; CHALCONE SYNTHASE; DNA BINDING PROTEIN; ELONGATION FACTOR; ELONGATION FACTOR TU; FLAVONOID; GIBBERELLIC ACID; GLUCOSE 6 PHOSPHATASE; GLUTAMATE AMMONIA LIGASE; HIGH MOBILITY GROUP B1 PROTEIN; INITIATION FACTOR 5A; MALATE DEHYDROGENASE; PEROXIDASE; PHOSPHOGLYCERATE KINASE; PHYTOHORMONE; PROTEIN DISULFIDE ISOMERASE; RIBOSOME PROTEIN; RIBULOSEBISPHOSPHATE CARBOXYLASE; TRANSALDOLASE; VEGETABLE PROTEIN;

ARTICLE; DIMOCARPUS LONGAN; DOWN REGULATION; FLORAL REVERSION; FLOWERING; MATRIX ASSISTED LASER DESORPTION IONIZATION TIME OF FLIGHT MASS SPECTROMETRY; NONHUMAN; NUCLEOTIDE SEQUENCE; PHOTOSYNTHESIS; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN ISOLATION; PROTEIN METABOLISM; PROTEIN STRUCTURE; PROTEOMICS; STRESS; TRANSCRIPTION REGULATION; TRANSMISSION ELECTRON MICROSCOPY; TREE; TWO DIMENSIONAL GEL ELECTROPHORESIS; UPREGULATION;

ANGIOSPERMS; CYTOSKELETON; DOWN-REGULATION; ELECTROPHORESIS, GEL, TWO-DIMENSIONAL; FLOWERS; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION, PLANT; HUMANS; MASS SPECTROMETRY; MICROSCOPY, ELECTRON, TRANSMISSION; PHOTOSYNTHESIS; PLANT PROTEINS; PROTEOMICS; SAPINDACEAE; SPECTROMETRY, MASS, MATRIX-ASSISTED LASER DESORPTION-IONIZATION; UP-REGULATION;

DIMOCARPUS LONGAN;

EID: 84855885054     PISSN: 18743919     EISSN: 18767737     Source Type: Journal    
DOI: 10.1016/j.jprot.2011.10.023     Document Type: Article

References (42)

1. Battley N.H., Lyndon R.F. Reversion of flowering. Bot Rev 1990, 56:162-189.
2. McCullough E., Wright K.M., Alvarez A., Clark C.P., Rickoll W.L., Madlung A. Photoperiod-dependent floral reversion in the natural allopolyploid Arabidopsis suecica. New Phytol 2010, 186(1):239-250.
3. Colasanti J., Yuan Z., Sundaresan V. The indeterminate gene encodes a zinc finger protein and regulates a leaf-generated signal required for the transition to flowering in maize. Cell 1998, 93:593-603.
4. Chen S.S., Liu H., Chen W., Xie D.L., Zheng S.Q. Proteomic analysis of differentially expressed proteins in longan flowering reversion buds. Sci Hortic 2009, 122:275-280.
5. Lyndon R.F. The shoot apical meristem: its growth and development. New Phytol 1999, 144(1):51-54.
6. Carolyn F.W., Judith F.T. Reversion of flowering in Glycine max (Fabaceae). Am J Bot 2000, 87:1425-1438.
7. Irish E., Nelson T.M. Identification of multiple stages in the conversion of maize meristems from vegetative to floral development. Development 1991, 112:891-898.
8. Huala E., Sussex I.M. Determination and cell interactions in reproductive meristems. Plant Cell 1993, 5:1157-1165.
9. Boss P.K., Bastow R.M., Mylne J.S., Dean C. Multiple pathways in the decision to flower: enabling, promoting and resetting. Plant Cell 2004, 16:S18-S31.
10. Fornara F., Gregis V., Pelucchi N., Colombo L., Kater M. The rice StMADS11-like genes OsMADS22 and OsMADS47 cause floral reversions in Arabidopsis without complementing the svp and agl24 mutants. J Exp Bot 2008, 59(8):2181-2190.
11. Saravanan R.S., Rose J.K. A critical evaluation of sample extraction techniques for enhanced proteomic analysis of recalcitrant plant tissues. Proteomics 2004, 4(9):2522-2532.
12. Bevan M., Bancroft I., Bent E., Love K., Goodman H., Dean C., et al. Analysis of 1.9Mb of contiguous sequence from chromosome 4 of Arabidopsis thaliana. Nature 1998, 391:485-488.
13. Clements J., Craig A. Characterization of a non-abscission mutant in Lupinus angustifolius. I. Genetic and structural aspects. Am J Bot 2001, 88:31-42.
14. Suzuki K., Takeda H., Tsukaguchi T., Egawa Y. Ultrastructural study on degeneration of tapetum in anther of snap bean (Phaseolus vulgaris L.) under heat stress. Sex Plant Reprod 2001, 13:293-299.
15. Macnish A.J., Irving D.E., Joyce D.C., Vithanage V., Wearing A.H. Anatomy of ethylene-induced floral-organ abscission in Chamelaucium uncinatum (Myrtaceae). Aust J Bot 2005, 53:119-131.
16. Gothandam K.M., Kim E.S., Chun Y.Y. Ultrastructural study of rice tapetum under low-temperature stress. J Plant Biol 2007, 50:396-402.
17. Delap A.V. The effect of supplying nitrate at different seasons on the growth, blossoming and nitrogen content of young apple tree in sand culture. J Horticultural Sci 1967, 42:149-167.
18. Corbesier L., Bernier G., Périlleux C. C:N ratio increases in the phloem sap during floral transition of the long-day plants Sinapis alba and Arabidopsis thaliana. Plant Cell Physiol 2001, 43:684-688.
19. Bower J.P., Cutting G.M., Lovatt C.J., Blanke M.M. Interaction of plant growth regulator and carbohydrate in flowering and fruit set. Acta Hortic 1990, 275:425-434.
20. Lin S.Q., Hu Y.L. Flowering reversion and its control of longan. Plant Physiol Commun 2001, 37(6):581-583.
21. Wu D., Qiu J., Zhang H.L., Luo X.Z. A study on flowering promotion by ringing in longan (Dimocarpus longana Lour.). Sci Agric Sin 2000, 33(6):40-43.
22. Lolas I.B., Himanen K., Grønlund J.T., Lynggaard C., Houben A., Melzer M., et al. The transcript elongation factor FACT affects Arabidopsis vegetative and reproductive development and genetically interacts with HUB1/2. Plant J 2010, 61(4):686-697.
23. Feng H.Z., Chen Q.G., Feng J. Functional characterization of the Arabidopsis eukaryotic translation initiation factor 5A-2 that plays a crucial role in plant growth and development by regulating cell division, cell growth, and cell death. Plant Physiol 2007, 7(144):1531-1545.
24. Koes R.E., Quattrocchio F., Mol J.M. The flavonoid biosynthetic pathway in plants: function and evolution. Bioessays 2005, 16(2):123-132.
25. Ma S.R., Zu Y.G. Correlations of endogenous hormones and flavonoids and flower bud differentiation in leaves in Catharanthus roseus. J Northeast For Univ 2009, 37(5):72-73.
26. Li N., You X.J., Peng J.Y., Wang J.R. Comparative study on yield and quality of flower buds of Lonicera japonica within several flowering stages. China J Chin Mater Med 2009, 34(11):1346-1350.
27. Sehnke P.C., DeLille J.M., Ferl R.J. Consummating signal transduction: the role of 14-3-3 proteins in the completion of signal-induced transitions in protein activity. Plant Cell 2002, 14:339-354.
28. Roberts M.R. 14-3-3 proteins find new partners in plant cell signaling. Trends Plant Sci 2003, 8:218-223.
29. Michael R.R., Julio S., David B.C. 14-3-3 proteins and the response to abiotic and biotic stress. Plant Mol Biol 2002, 50(6):1031-1039.
30. Xu W.F., Shi W.M. Expression profiling of the 14-3-3 gene family in response to salt stress and potassium and iron deficiencies in young tomato (Solanum lycopersicum) roots: analysis by real-time RT-PCR. Ann Bot 2006, 98(5):965-974.
31. Shanko A.V., Mesenko M.M., Klychnikov O.I., Nosov A.V., Ivanov V.B. Proton pumping in growing part of maize root: its correlation with 14-3-3 protein content and changes in response to osmotic stress. Biochem Mosc 2003, 68(12):1320-1326.
32. +-pump activity by 14-3-3 proteins in barley (Hordeum disticum) roots under salt stress. Russ J Plant Physiol 2002, 49(6):754-760.
33. Li Q.T., Yan J.Q., Wang J., Zhang H. The roles of an Arabidopsis 14-3-3 protein, GF14 lambda, and its interacting proteins in antioxidation metabolism and stress tolerance. Recent research developments in plant molecular biology 2003, 1:57-65.
34. Yan J.Q., He C.X., Wang J., Mao Z.H., Holaday S.A., Allen R.D., et al. Overexpression of the Arabidopsis 14-3-3 protein GF14 lambda in cotton leads to a "stay-green" phenotype and improves stress tolerance under moderate drought conditions. Plant Cell Physiol 2004, 45(8):1007-1014.
35. Tetsuo O., Masaji K., Kiyohide K., Hitoshi Y., Motoshige K. A role of OsGA20ox1, encoding an isoform of gibberellin 20-oxidase, for regulation of plant stature in rice. Plant Mol Biol 2004, 55(5):687-700.
36. Vidal A.M., Gisbert C., Talon M., Primo M.E., Lopez D.I., Garcia-Martinez J.L. The ectopic overexpression of a citrus gibberellin 20-oxidase enhances the non-13-hydroxylation pathway of gibberellin biosynthesis and induces an extremely elongated phenotype in tobacco. Physiol Plant 2001, 112(2):251-260.
37. 3 on the mechanism of flower bud induction in apple tree. Acta Harticulturae Sin 2001, 28(4):339-341.
38. Liu H.B., Lin Z.L., Chen S.Q. Time course changes of endogenous hormone levels during the floral and vegetative buds formation in loquat (Eriobotrya japonica Lind1.). Acta Harticulturae Sin 2007, 34(2):339-344.
39. Li X.Z., Li J., Deng L. Differentiation of the sweet orange trees by overcropping and spraying with GA. Sci Agric Sin 1992, 25(3):72-75.
40. Xiao H.S., Lv L.X., Chen Z.T. Dynamic changes of endogenous hormone in litchi (Litchi chinensis Sonn.) pistil and stamen during flower development. Chin J Appl Environ Biol 2003, 9(1):11-15.
41. Huang Q.W. Changes in endogenous hormone contents in relation to flower bud differentiation and on-year or off-year fruiting of longan. J Trop Subtrop Bot 1996, 4(2):58-62.
42. Qiu J.D., Wu D.Y., Zhang H.L. A study on flower differentiation of 'Shixia' longan (Dimocarpus longana Lour. cv. Shixia). J South China Agric Univ 2001, 22(1):27-30.