Anthocyanin biosynthesis and accumulation in developing flowers of tree peony (Paeonia suffruticosa) 'Luoyang Hong'

Postharvest Biology and Technology

Volumn 97, Issue , 2014, Pages 11-22

  Zhang, Chao ^a   Wang, Weining ^a   Wang, Yanjie ^a   Gao, Shulin ^a   Du, Danni ^a   Fu, Jianxin ^a   Dong, Li ^a  

^a BEIJING FORESTRY UNIVERSITY   (China)

Author keywords

Anthocyanin biosynthesis; Flower color; Paeonia suffruticosa; Regulatory genes; Structural genes

Indexed keywords

EID: 84904678792     PISSN: 09255214     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.postharvbio.2014.05.019     Document Type: Article

References (58)

1. Biran I., Halevy A.H. Effects of varying light intensities and temperature treatments applied to whole plants, or locally to leaves or flower buds, on growth and pigmentation of 'Baccara' roses. Physiol. Plant. 1974, 31:175-179.
2. Borevitz J.O., Xia Y., Blount J., Dixon R.A., Lamb C. Activation tagging identifies a conserved MYB regulator of phenylpropanoid biosynthesis. Plant Cell 2000, 12:2383-2393.
3. Castellarin S.D., Di Gaspero G., Marconi R., Nonis A., Peterlunger E., Paillard S., Adam-Blondon A.-F., Testolin R. Colour variation in red grapevines (Vitis vinifera L.): genomic organisation, expression of flavonoid 3'-hydroxylase, flavonoid 3',5'-hydroxylase genes and related metabolite profiling of red cyanidin-/blue delphinidin-based anthocyanins in berry skin. BMC Genomics 2006, 7:12.
4. Chang S., Puryear J., Cairney J. A simple and efficient method for isolating RNA from pine trees. Plant Mol. Biol. Rep. 1993, 11:113-116.
5. Das P.K., Shin D.H., Choi S.-B., Park Y.-I. Sugar-hormone cross-talk in anthocyanin biosynthesis. Mol. Cells 2012, 34:501-507.
6. Davies K.M., Albert N.W., Schwinn K.E. From landing lights to mimicry: the molecular regulation of flower colouration and mechanisms for pigmentation patterning. Funct. Plant Biol. 2012, 39:619-638.
7. Dela G., Or E., Ovadia R., Nissim-Levi A., Weiss D., Oren-Shamir M. Changes in anthocyanin concentration and composition in 'Jaguar' rose flowers due to transient high-temperature conditions. Plant Sci. 2003, 164:333-340.
8. Deluc L., Barrieu F., Marchive C., Lauvergeat V., Decendit A., Richard T., Carde J.-P., Mérillon J.-M., Hamdi S. Characterization of a grapevine R2R3-MYB transcription factor that regulates the phenylpropanoid pathway. Plant Physiol. 2006, 140:499-511.
9. Deluc L., Bogs J., Walker A.R., Ferrier T., Decendit A., Merillon J.-M., Robinson S.P., Barrieu F. The transcription factor VvMYB5b contributes to the regulation of anthocyanin and proanthocyanidin biosynthesis in developing grape berries. Plant Physiol. 2008, 147:2041-2053.
10. Faragher J., Brohier R. Anthocyanin accumulation in apple skin during ripening: regulation by ethylene and phenylalanine ammonia-lyase. Sci. Hortic. 1984, 22:89-96.
11. Feller A., Machemer K., Braun E.L., Grotewold E. Evolutionary and comparative analysis of MYB and bHLH plant transcription factors. Plant J. 2011, 66:94-116.
12. Forkmann G. Flavonoids as flower pigments: the formation of the natural spectrum and its extension by genetic engineering. Plant Breed. 1991, 106:1-26.
13. Griesbach R. Correlation of pH and light intensity on flower color in potted Eustoma grandiflorum Grise. HortScience 1992, 27:817-818.
14. Guo W.W., Dong L., Wang L.Y., Chen R.X., Liu A.Q. The postharvest characteristics and water balance of some cultivars of tree-peony cut flowers. Sci. Silvae Sin. 2004, 40:89-93.
15. Han K.T., Zhao L., Tang X.J., Hu K., Dai S.L. The relationship between the expression of key genes in anthocyanin biosynthesis and the color of chrysanthemum. Acta Hortic. Sin. 2012, 39:516-524.
16. Hichri I., Barrieu F., Bogs J., Kappel C., Delrot S., Lauvergeat V. Recent advances in the transcriptional regulation of the flavonoid biosynthetic pathway. J. Exp. Bot. 2011, 62:2465-2483.
17. Hichri I., Heppel S.C., Pillet J., Léon C., Czemmel S., Delrot S., Lauvergeat V., Bogs J. The basic helix-loop-helix transcription factor MYC1 is involved in the regulation of the flavonoid biosynthesis pathway in grapevine. Mol. Plant 2010, 3:509-523.
18. Holton T.A., Cornish E.C. Genetics and biochemistry of anthocyanin biosynthesis. Plant Cell 1995, 7:1071-1083.
19. Hosoki T., Hamada M., Kando T., Moriwaki R., Inaba K. Comparative study of anthocyanins in tree peony flowers. J. Jpn. Soc. Hortic. Sci. 1991, 60:395-403.
20. Ichimura K., Kojima K., Goto R. Effects of temperature, 8-hydroxyquinoline sulphate and sucrose on the vase life of cut rose flowers. Postharvest Biol. Technol. 1999, 15:33-40.
21. Jackson D., Roberts K., Martin C. Temporal and spatial control of expression of anthocyanin biosynthetic genes in developing flowers of Antirrhinum majus. Plant J. 1992, 2:425-434.
22. Jamal Uddin A., Hashimoto F., Kaketani M., Shimizu K., Sakata Y. Analysis of light and sucrose potencies on petal coloration and pigmentation of lisianthus cultivars (in vitro). Sci. Hortic. 2001, 89:75-84.
23. Jia P.Y., Zhou L., Guo W.W., Wang L.Y., Dong L. Postharvest behavior and endogenous ethylene pattern of Paeonia suffruticosa cut flowers. Acta Hortic. 2008, 768:445-450.
24. Lai Y.-S., Yamagishi M., Suzuki T. Elevated temperature inhibits anthocyanin biosynthesis in the tepals of an Oriental hybrid lily via the suppression of LhMYB12 transcription. Sci. Hortic. 2011, 132:59-65.
25. Li J.J. Chinese Tree and Herbaceous Peonies 1999, China Forestry Publishing House, Beijing.
26. Liu X., Feng C., Zhang M., Yin X., Xu C., Chen K. The MrWD40-1 gene of Chinese bayberry (Myrica rubra) interacts with MYB and bHLH to enhance anthocyanin accumulation. Plant Mol. Biol. Rep. 2013, 31:1474-1484.
27. Matus J., Poupin M., Cañón P., Bordeu E., Alcalde J., Arce-Johnson P. Isolation of WDR and bHLH genes related to flavonoid synthesis in grapevine (Vitis vinifera L.). Plant Mol. Biol. 2010, 72:607-620.
28. Meir S., Kochanek B., Glick A., Salim S., Lers A., Burd S., Philosoph-Hadas S., Weiss D. Reduced petal rigmentation in lisianthus (Eustoma grandiflorum) flowers under low light conditions is associated with decreased expression of anthocyanin biosynthesis genes. Acta Hortic. 2009, 877:1735-1744.
29. Minakuchi S., Ichimura K., Nakayama M., Hisamatsu T., Koshioka M. Effects of high-sucrose concentration treatments on petal color pigmentation and concentrations of sugars and anthocyanins in petals of bud cut carnations (Dianthus caryophyllus). Hortic. Res. 2008, 7:277-281.
30. Mol J., Grotewold E., Koes R. How genes paint flowers and seeds. Trends Plant Sci. 1998, 3:212-217.
31. Moscovici S., Moalem-Beno D., Weiss D. Leaf-mediated light responses in petunia flowers. Plant Physiol. 1996, 110:1275-1282.
32. Nakatsuka A., Mizuta D., Kii Y., Miyajima I., Kobayashi N. Isolation and expression analysis of flavonoid biosynthesis genes in evergreen azalea. Sci. Hortic. 2008, 118:314-320.
33. Nakatsuka T., Nishihara M., Mishiba K., Yamamura S. Temporal expression of flavonoid biosynthesis-related genes regulates flower pigmentation in gentian plants. Plant Sci. 2005, 168:1309-1318.
34. Noda N., Kanno Y., Kato N., Kazuma K., Suzuki M. Regulation of gene expression involved in flavonol and anthocyanin biosynthesis during petal development in lisianthus (Eustoma grandiflorum). Physiol. Plant. 2004, 122:305-313.
35. Quattrocchio F., Wing J.F., Va K., Mol J.N., Koes R. Analysis of bHLH and MYB domain proteins: species-specific regulatory differences are caused by divergent evolution of target anthocyanin genes. Plant J. 1998, 13:475-488.
36. Schwinn K., Venail J., Shang Y., Mackay S., Alm V., Butelli E., Oyama R., Bailey P., Davies K., Martin C. A small family of MYB-regulatory genes controls floral pigmentation intensity and patterning in the genus Antirrhinum. Plant Cell 2006, 18:831-851.
37. Tamura K., Dudley J., Nei M., Kumar S. MEGA4: molecular evolutionary genetics analysis (MEGA) software version 4.0. Mol. Biol. Evol. 2007, 24:1596-1599.
38. Voss D.H. Relating colourimeter measurement of plant colour to the Royal Horticultural Society Colour Chart. HortScience 1992, 27:1256-1260.
39. Wang L.-S., Hashimoto F., Shiraishi A., Aoki N., Li J.-J., Sakata Y. Chemical taxonomy of the Xibei tree peony from China by floral pigmentation. J. Plant Res. 2004, 117:47-55.
40. Wang L.-S., Shiraishi A., Hashimoto F., Aoki N., Shimizu K., Sakata Y. Analysis of petal anthocyanins to investigate flower coloration of Zhongyuan (Chinese) and Daikon Island (Japanese) tree peony cultivars. J. Plant Res. 2001, 114:33-43.
41. Wang Y., Zhang C., Jia P., Wang X., Wang W., Dong L. Isolation and expression analysis of three EIN3-like genes in tree peony (Paeonia suffruticosa). Plant Cell Tissue Organ Cult. 2013, 112:181-190.
42. Wang Y.J., Dong L., Zhang C., Wang X.Q. Reference gene gelection for real-time quantitative PCR normalization in tree peony (Paeonia suffruticosa Andr). J. Agric. Biotechnol. 2012, 20:521-528.
43. Weiss D. Regulation of flower pigmentation and growth: multiple signaling pathways control anthocyanin synthesis in expanding petals. Physiol. Plant. 2000, 110:152-157.
44. Winkel-Shirley B. Flavonoid biosynthesis. A colorful model for genetics, biochemistry, cell biology, and biotechnology. Plant Physiol. 2001, 126:485-493.
45. Winkel-Shirley B. It takes a garden. How work on diverse plant species has contributed to an understanding of flavonoid metabolism. Plant Physiol. 2001, 127:1399-1404.
46. Xie X.B., Li S., Zhang R.F., Zhao J., Chen Y.C., Zhao Q., Yao Y.X., You C.X., Zhang X.S., Hao Y.J. The bHLH transcription factor MdbHLH3 promotes anthocyanin accumulation and fruit colouration in response to low temperature in apples. Plant Cell Environ. 2012, 35:1884-1897.
47. Yamane T., Jeong S.T., Goto-Yamamoto N., Koshita Y., Kobayashi S. Effects of temperature on anthocyanin biosynthesis in grape berry skins. Am. J. Enol. Viticult. 2006, 57:54-59.
48. Zhang C., Liu M., Fu J., Wang Y., Dong L. Exogenous sugars involvement in senescence and ethylene production of tree peony 'Luoyang Hong' cut flowers. Korean J. Hortic. Sci. Technol. 2012, 30:718-724.
49. Zhang C., Wang Y., Fu J., Dong L., Gao S., Du D. Transcriptomic analysis of cut tree peony with glucose supply using the RNA-Seq technique. Plant Cell Rep. 2014, 33:111-129.
50. Zhang F., Gonzalez A., Zhao M., Payne C.T., Lloyd A. A network of redundant bHLH proteins functions in all TTG1-dependent pathways of Arabidopsis. Development 2003, 130:4859-4869.
51. Zhang J., Wang L., Shu Q., Liu Z., Li C., Zhang J., Wei X., Tian D. Comparison of anthocyanins in non-blotches and blotches of the petals of Xibei tree peony. Sci. Hortic. 2007, 114:104-111.
52. Zhao D., Tao J., Han C., Ge J. Flower color diversity revealed by differential expression of flavonoid biosynthetic genes and flavonoid accumulation in herbaceous peony (Paeonia lactiflora Pall.). Mol. Biol. Rep. 2012, 39:11263-11275.
53. Zhou L., Dong L., Jia P.Y., Wang W.R., Wang L.Y. Expression of ethylene receptor and transcription factor genes, and ethylene response during flower opening in tree peony (Paeonia suffruticosa). Plant Growth Regul. 2010, 62:171-179.
54. Zhou L., Wang Y., Peng Z. Isolation and tissue-specific expression of chalcone synthase gene Ps-CHS1 in tree peony. Acta Hortic. Sin. 2010, 37:1295-1302.
55. Zhou L., Wang Y., Peng Z. Molecular characterization and expression analysis of chalcone synthase gene during flower development in tree peony (Paeonia suffruticosa). Afr. J. Biotechnol. 2011, 10:1275-1284.
56. Zhou L., Wang Y., Ren L., Peng Z. Cloning and expression analysis of dihydroflavonol 4-reductase gene PsDFR1 from tree peony (Paeonia suffruticosa Andr). Plant Physiol. J. 2011, 47:885-892.
57. Zhou L., Wang Y., Ren L., Shi Q., Zheng B., Miao K., Guo X. Overexpression of Ps-CHI1, a homologue of the chalcone isomerase gene from tree peony (Paeonia suffruticosa), reduces the intensity of flower pigmentation in transgenic tobacco. Plant Cell Tissue Organ Cult. 2014, 116:285-295.
58. Zimmermann I.M., Heim M.A., Weisshaar B., Uhrig J.F. Comprehensive identification of Arabidopsis thaliana MYB transcription factors interacting with R/B-like BHLH proteins. Plant J. 2004, 40:22-34.