Trichomes: different regulatory networks lead to convergent structures

Trends in Plant Science

Volumn 11, Issue 6, 2006, Pages 274-280

  Serna, Laura ^a   Martin, Cathie ^b  

^a UNIVERSITY OF CASTILLA LA MANCHA   (Spain)

^b JOHN INNES CENTRE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ANTHOCYANIN; ARABIDOPSIS PROTEIN; ATR1 PROTEIN, ARABIDOPSIS; CPC PROTEIN, ARABIDOPSIS; MYB PROTEIN, PLANT; PROTEIN C MYB; VEGETABLE PROTEIN;

ANGIOSPERM; ANTIRRHINUM; ARABIDOPSIS; ARTICLE; BIOSYNTHESIS; COTTON; GENETICS; GROWTH, DEVELOPMENT AND AGING; PHYLOGENY; PHYSIOLOGY; REGULATORY SEQUENCE;

ANTHOCYANINS; ANTIRRHINUM; ARABIDOPSIS; ARABIDOPSIS PROTEINS; GOSSYPIUM; PHYLOGENY; PLANT PROTEINS; PROTO-ONCOGENE PROTEINS C-MYB; REGULATORY ELEMENTS, TRANSCRIPTIONAL; SOLANACEAE;

ANTIRRHINUM; ARABIDOPSIS; ARABIDOPSIS THALIANA; GOSSYPIUM HIRSUTUM;

EID: 33744993149     PISSN: 13601385     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tplants.2006.04.008     Document Type: Article

References (68)

1. Werker E. Trichome diversity and development. Adv. Bot. Res. 31 (2000) 1-35
2. Johnson H.B. Plant pubescence: an ecological perspective. Bot. Rev. 41 (1975) 233-258
3. Mauricio R., and Rausher M.D. Experimental manipulation of putative selective agents provides evidence for the role of natural enemies in the evolution of plant defense. Evolution Int. J. Org. Evolution 51 (1997) 1435-1444
4. Wilkins T.A., et al. Cotton biotechnology. Crit. Rev. Plant Sci. 19 (2000) 511-550
5. Chen L., et al. Convergent evolution of antifreeze glycoproteins in Antarctic notothenioid fish and Arctic cod. Proc. Natl. Acad. Sci. U. S. A. 94 (1997) 3817-3822
6. Oakley T.H., and Cunningham C.W. Molecular phylogenetic evidence for the independent evolutionary origin of an arthropod compound eye. Proc. Natl. Acad. Sci. U. S. A. 99 (2002) 1426-1430
7. Marks M.D., and Feldmann K.A. Trichome development in Arabidopsis thaliana. I. T-DNA tagging of the GLABROUS1 gene. Plant Cell 1 (1989) 1043-1050
8. Oppenheimer D.G., et al. A myb gene required for leaf trichome differentiation in Arabidopsis is expressed in stipules. Cell 67 (1991) 483-493
9. Grotewold E., et al. Identification of the residues in the Myb domain of maize C1 that specify the interaction with the bHLH cofactor R. Proc. Natl. Acad. Sci. U. S. A. 25 (2000) 13579-13584
10. Winkel-Shirley B. Flavonoid biosyntheis. A colour model for genetics, biochemistry, cell biology, and biotechnology. Plant Physiol. 126 (2001) 485-493
11. Zimmermann I.M., et al. Comprehensive identification of Arabidopsis thaliana MYB transcription factors interacting with R/B-like BHLH proteins. Plant J. 40 (2004) 22-34
12. Kirik V., et al. Ectopic expression of the Arabidopsis AtMYB23 gene induces differentiation of trichome cells. Development 235 (2001) 366-377
13. Kirik V., et al. Functional diversification of MYB23 and GL1 genes in trichome morphogenesis and initiation. Development 132 (2005) 1477-1485
14. Payne C.T., et al. GL3 encodes a bHLH protein that regulates trichome development in Arabidopsis through interaction with GL1 and TTG1. Genetics 156 (2000) 1349-1362
15. Zhang F., et al. A network of redundant bHLH proteins functions in all TTG1-dependent pathways of Arabidopsis. Development 130 (2003) 4859-4869
16. Walker A.R., et al. The TRANSPARENT TESTA GLABRA1 locus, which regulates trichome differentiation and anthocyanin biosynthesis in Arabidopsis, encodes a WD40 repeat protein. Plant Cell 11 (1999) 1337-1349
17. Koornneef M. The complex syndrome of ttg mutants. Arabidopsis Inf. Serv. 18 (1981) 45-51
18. Hülskamp M., et al. Genetic dissection of trichome cell development in Arabidopsis. Cell 76 (1994) 555-556
19. Schnittger A., et al. Tissue layer and organ specificity of trichome formation are regulated by GLABRA1 and TRIPTYCHON in Arabidopsis. Development 125 (1998) 2283-2289
20. Schnittger A., et al. Generation of a spacing pattern: the role of TRIPTYCHON in trichome patterning in Arabidopsis. Plant Cell 11 (1999) 1105-1116
21. Schellmann S., et al. TRIPTYCHON and CAPRICE mediate lateral inhibition during trichome and root hair patterning in Arabidopsis. EMBO J. 21 (2002) 5036-5046
22. Kirik V., et al. The ENHANCER OF TRY AND CPC1 gene acts redundantly with TRIPTYCHON and CAPRICE in trichome and root hair cell patterning in Arabidopsis. Dev. Biol. 268 (2004) 506-513
23. Kirik V., et al. ENHANCER of TRY and CPC2 (ETC2) reveals redundancy in the region-specific control of trichome development of Arabidopsis. Plant Mol. Biol. 55 (2004) 389-398
24. Koshino-Kimura Y., et al. Regulation of CAPRICE transcription by MYB proteins for root epidermis differentiation in Arabidopsis. Plant Cell Physiol. 46 (2005) 817-826
25. Larkin J.C., et al. How cells know what they want to be when they grow up? Lessons from epidermal patterning in Arabidopsis. Annu. Rev. Plant Biol. 54 (2003) 403-430
26. Schiefelbein J. Cell-fate specification in the epidermis: a common patterning mechanism in the root and shoot. Curr. Opin. Plant Biol. 6 (2003) 74-78
27. Esch J.J., et al. A contradictory GLABRA3 allele helps define gene interactions controlling trichome development in Arabidopsis. Development 130 (2003) 5885-5894
28. Hülskamp M. Plant trichomes: a model for cell differentiation. Nat. Rev. Mol. Cell Biol. 5 (2004) 471-480
29. Serna L. A network of interacting factors triggering different fates. Plant Cell 16 (2004) 2258-2263
30. Szymanski D.B., et al. Control of GL2 expression in Arabidopsis leaves and trichomes. Development 125 (1998) 1161-1171
31. Wang S., et al. Control of plant trichome development by a cotton fiber MYB gene. Plant Cell 16 (2004) 2323-2334
32. Suo J., et al. Identification of GhMYB109 encoding a R2R3 MYB transcriptional factor that expresses specifically in fiber initials and elongating fibers of cotton (Gossypium hirsutum L.). Biochim. Biophys. Acta 1630 (2003) 25-34
33. Humphries J.A., et al. Two WD-repeat genes from cotton are functional homologues of the Arabidopsis thaliana TRANSPARENT TESTA GLABRA1 (TTG1) gene. Plant Mol. Biol. 57 (2005) 67-81
34. Noda K.-I., et al. Flower colour intensity depends on specialized cell shape controlled by a Myb-related transcription factor. Nature 369 (1994) 661-664
35. Glover B.J., et al. Development of several epidermal cell types can be specified by the same MYB-related plant transcriptional factor. Development 125 (1998) 3497-3508
36. Martin C., et al. The mechanics of cell fate determination in petals. Philos. Trans. R. Soc. Lond. B Biol. Sci. 357 (2002) 809-813
37. Martin C., and Paz-Ares J. MYB transcription factors in plants. Trends Genet. 13 (1997) 67-73
38. Payne T., et al. Heterologous myb genes distinct from GL1 enhance trichome production when overexpressed in Nicotiana tabacum. Development 126 (1999) 671-682
39. Glover B.J., et al. Convergent evolution within the genus Solanum: the specialised anther cone develops through alternative pathways. Gene 331 (2004) 1-7
40. Avila A., et al. Petunia hybrida genes related to the maize regulatory C1 gene and to the animal myb proto-oncogenes. Plant J. 3 (1993) 553-562
41. van Houwelingen A., et al. Analysis of flower pigmentation mutants generated by random transposon mutagenesis in Petunia hybrida. Plant J. 13 (1998) 39-50
42. Perez-Rodriguez M., et al. Development of three different cell types is associated with the activity of a specific MYB transcription factor in the ventral petal of Anthirrhinum majus flowers. Development 132 (2005) 359-379
43. Lloyd A.M., et al. Arabidopsis and Nicotiana anthocyanin production activated by maize regulators R and C1. Science 258 (1992) 1773-1775
44. Mooney M., et al. Altered regulation of tomato and tobacco pigmentation genes caused by delila gene of Antirrhinum. Plant J. 7 (1995) 333-339
45. Quattrocchio F., et al. Regulatory genes controlling anthocyanin pigmentation are functionally conserved among plant species and have distinct sets of target genes. Plant Cell 5 (1993) 1497-1512
46. Spelt C., et al. anthocyanin1 of petunia encodes a basic-helix loop helix protein that directly activates structural anthocyanin genes. Plant Cell 12 (2000) 1619-1631
47. de Vetten N., et al. 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
48. Spelt C., et al. ANTHOCYANIN1 of petunia controls pigment synthesis, vacuolar pH, and seed coat development by genetically distinct mechanism. Plant Cell 14 (2002) 2121-2135
49. Carey C.C., et al. Mutations in the pale aleurone color1 regulatory gene of the Zea mays anthocyanin pathway have distinct phenotypes relative to the functionally similar TRANSPARENT TESTA GLABRA1 gene in Arabidopsis thaliana. Plant Cell 16 (2004) 450-464
50. Stracke R., et al. The R2R3-MYB gene family in Arabidopsis thaliana. Curr. Opin. Plant Biol. 4 (2001) 447-456
51. Goodspeed T.H. The genus Nicotiana. In: Verdoorn F. (Ed). Chronica Botanica (1954), Chronica Botanica Co 102-131
52. Borevitz J.O., et al. Activation tagging identifies a conserved MYB regulator of phenylpropanoid biosynthesis. Plant Cell 12 (2000) 2383-2393
53. Nesi N., et al. The TT8 gene encodes a basic helix-loop-helix domain protein required for expression of DFR and BAN genes in Arabidopsis siliques. Plant Cell 12 (2000) 1863-1878
54. Nesi N., et al. The Arabidopsis TT2 gene encodes an R2R3 MYB domain protein that acts as a key determinant for proanthocyanidin accumulation in developing seed. Plant Cell 13 (2001) 2099-2114
55. Koes R., et al. Flavonoids: a colorful model for the regulation and evolution of biochemical pathways. Trends Plant Sci. 10 (2005) 236-242
56. Ramsay N.A., and Glover B.J. MYB-bHLH-WD40 protein complex and the evolution of cellular diversity. Trends Plant Sci. 10 (2005) 63-70
57. Mol J., et al. How genes paint flowers and seeds. Trends Plant Sci. 3 (1998) 212-217
58. Quattrocchio F., et al. Analysis of bHLH and MYB-domain proteins: species specific regulatory differences are caused by divergent evolution of target anthocyanin genes. Plant J. 13 (1998) 457-488
59. Gong, Z.Z. et al. (1999a) A constitutively expressed Myc-like gene involved in anthocyanin biosynthesis from Perilla frutescens: molecular characterization, heterologous expression in transgenic plants and transactivation in yeast cells. Plant Mol. Biol. 41, 33-44
60. Gong, Z.Z. et al. (1999a) A constitutively expressed Myc-like gene involved in anthocyanin biosynthesis from Perilla frutescens: molecular characterization, heterologous expression in transgenic plants and transactivation in yeast cells. Plant Mol. Biol. 41, 33-44
61. Sompornpailin K., et al. A WD-repeat-containing putative regulatory protein in anthocyanin biosynthesis in Perilla frutescens. Plant Mol. Biol. 50 (2002) 485-495
62. Elomaa P., et al. A bHLH transcriptional factor mediates organ, region and flower type specific signals on dihydroflavonol-4-reductase (dfr) gene expression in the inflorescence of Gerbera hybrida (Asteraceae). Plant J. 16 (1998) 93-99
63. Elomaa P., et al. Activation of anthocyanin biosynthesis in Gerbera hybrida (Asteraceae) suggests conserved protein-protein and protein-promoter interactions between the anciently diverged monocots and eudicots. Plant Physiol. 133 (2003) 1831-1842
64. Ohno S. Evolution by Gene Duplication (1970), Springer-Verlag
65. Zhang J. Evolution by gene duplication: an update. Trends Ecol. Evol. 18 (2003) 292-298
66. Leech M.J., et al. Expression of myb-related genes in the moss Physcomitrella patens. Plant J. 3 (1993) 51-61
67. Cove D.J., and Ashton N.W. Growth regulation and development in Physcomitrella patens: an insight into growth regulation and development of bryophytes. Bot. J. Linnean Soc. 98 (1988) 247-252
68. Celenza J.L., et al. The Arabidopsis ATR1 Myb transcription factor controls indolic glucosinolate homeostasis. Plant Physiol. 137 (2005) 253-262