Chapter Eight Mechanisms and applications of transcriptional control of phenylpropanoid metabolism

Recent Advances in Phytochemistry

Volumn 35, Issue C, 2001, Pages 155-169

  Martin, Cathie ^a   Jin, Hailing ^a   Schwinn, Kathy ^a  

^a JOHN INNES CENTRE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 77957056883     PISSN: 00799920     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0079-9920(01)80009-5     Document Type: Article

References (30)

1. Kacser H., Burns J.A., and Fell D.A. The control of flux. Biochem. Soc. Trans. 23 (1995) 341-366
2. Napoli C., Lemieux C., and Jorgensen R. Introduction of a chimeric chalcone synthase gene into petunia results in reversible, co-suppression of homologous genes in trans. Plant Cell 2 (1990) 279-289
3. Doebley J. Genetic development and plant evolution. Curr. Op. Genet. Dev. 3 (1993) 865-872
4. Doebley J., and Lukens L. Transcriptional regulators and the evolution of plant form. Plant Cell 10 (1998) 1075-1082
5. Van Der Fits L., and Memelink J. ORCA3, a jasmonate-responsive transcriptional regulator of plant primary and secondary metabolism. Science 289 (2000) 295-297
6. Menke F.L.H., Champion A., Kijne J.W., and Memelink J. A novel asmonate- and elicitor-responsive element in the periwinkle secondary metabolite biosynthetic gene Str interacts with a jasmonate- and elicitor-inducible AP2-domain transcription factor. ORCA2, EMBO J. 18 (1999) 4455-4463
7. Bender J., and Fink G.R. A Myb homologue, ATR1, activates tryptophan gene expression in Arabidopsis. Proc. Natl. Acad. Sci. USA 95 (1998) 5655
8. Ragg H., Kuhn D.N., and Hahlbrock K. Coordinated regulation of 4-coumarate-CoA ligase and phenylalanine ammonia-lyase messenger-RNAs in cultured plant-cells. J. Biol. Chem. 256 (1981) 61-651
9. Dooner H.K. Coordinate genetic-regulation of flavonoid biosynthetic-enzymes in maize. Mol. Gen. Genet. 189 (1983) 136-141
10. Pazares J., Wienand U., Peterson P.A., and Saedler H. Molecularcloning of the C-locus, of Zea mays-a locus regulating the anthocyanin pathway. EMBO J. 5 (1986) 829-833
11. Ludwig S.R., Habera L.F., Dellaporta S.L., and Wessler S.R. Lc, a member of the maize R-gene family responsible for tissue-specific anthocyanin production, encodes a protein similar to transcriptional activators and contains the myc-homology region. Proc. Natl. Acad. Sci. USA 86 (1989) 7092-7096
12. Goodrich J., Carpenter R., and Coen E.S. A common gene regulates pigmentation pattern in diverse plant-species. Cell 68 (1992) 955-964
13. Lloyd A.M., Walbot V., and Davis R.W. Arabidopsis and Nicotiana anthocyanin production activated by maize regulator-R and regulator-C1. Science 258 (1992) 1773-1775
14. Mooney M., Desnos T., Harrison K., Jones J., Carpenter R., and Coen E. Altered regulation of tomato and tobacco pigmentation genes caused by the Delila gene of Antirrhinum. Plant J. 7 (1995) 333-339
15. Quattrocchio F., Wing J.F., Van der Woude K., Mol J.N.M., and Koes R. Analysis of bHLH and MYB domain proteins: species-specific regulatory differences are caused by divergent evolution of target anthocyanin genes. Plant J. 13 (1998) 475-488
16. De Vetten N., Quattrocchio F., Mol J., and Koes R. The an11 locus controlling flower pigmentation in petunia encodes a novel WD-repeat protein conserved in yeast, plants, and animals. Genes Dev. 11 (1997) 1422-1434
17. Quattrocchio F., Wing J.F., Leppen H.T.C., Mol J.N.M., and Koes R.E. Regulatory genes-controlling anthocyanin pigmentation are functionally conserved among plant-species and have distinct sets of target genes. Plant Cell 5 (1993) 1497-1512
18. Martin C., Prescott A., Mackay S., Bartlett J., and Vrijlandt E. Control of anthocyanin biosynthesis in flowers of Antirrhinum majus. Plant J. 1 (1991) 37-49
19. Chandler V.L., Radicella J.P., Robbins T.P., Chen J.C., and Turks D. Two regulatory genes of the maize anthocyanin, pathway are homologous-isolation of B utilizing R genomic sequences. Plant Cell 1 (1989) 1175-1183
20. Cone K.C., Cocciolone S.M., Burr F.A., and Burr B. Maize anthocyanin regulatory gene Pl is a duplicate of C1 that functions in the plant. Plant Cell 5 (1993) 1795-1805
21. Schwinn K. The Control of Anthocyanin Bisynthesis in Antirrhinum majus. PhD Thesis (2000), University of East Anglia
22. Weisshaar B., Armstrong G.A., Block A., De Silva O., and Hahlbrock K. Light-inducible and constitutively expressed DNA-binding proteins recognizing a plant promoter element with functional relevance in light responsiveness. EMBO J. 10 (1991) 1777-1786
23. Sablowski R.W.M., Moyano E., Culianez-Macia F.A., Schuch W., Martin C., and Bevan M. A flower-specific MYB protein activates transcription of phenylpropanoid biosynthetic genes. EMBO J. 13 (1994) 128-137
24. Moyano E., Martinezgarcia J.F., and Martin C. Apparent redundancy in Myb gene function provides gearing for the control of flavonoid biosynthesis in Antirrhinum flowers. Plant Cell 8 (1996) 1519-1532
25. Tamagnone L., Merid A.A., Parr A., Mackay S., Culianezmacia F.A., Roberts K., and Martin C. The AmMYB308 and AmMYB330 transcription factors from antirrhinum regulate phenylpropanoid and lignin biosynthesis in transgenic tobacco. Plant Cell 10 (1998) 135-154
26. Jin H.L., Cominelli E., Bailey P., Parr A., Mehrtens F., Jones J., Tonelli C., Weisshaar B., and Martin C. Transcriptional repression by AtMYB4 controls production of UV-protecting sunscreens in Arabidopsis. EMBO J. 19 (2000) 6150-6161
27. Parr A.J., Waldron K.W., Ng A., and Parker M.L. The wall-bound phenolics of Chinese water chestnut (Eleocharis dulcis). J. Sci. Food Agric. 71 (1996) 501-507
28. De Gaulejac N.S., Glories Y., and Vivas N. Free radical scavenging effect of anthocyanins in red wines. Food Res. Int. 32 (1999) 327-333
29. Rice-Evans C.A., Miller N.J., and Paganga G. Antioxidant properties of phenolic compounds. Trends Plant Sci. 2 (1997) 152-159
30. Tamagnone L., Merida A., Stacey N., Plaskitt K., Parr A., Chang C.F., Lynn D., Dow J.M., Roberts K., and Martin C. Inhibition of phenolic acid metabolism results in precocious cell death and altered cell morphology in leaves of transgenic tobacco plants. Plant Cell 10 (1998) 1801-1816