|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
First published online 30 June 2004
doi: 10.1242/dev.01205
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||

1 Abteilung für Molekulare Pflanzengenetik, Max-Planck-Institut für
Züchtungsforschung, 50829 Köln, Germany
2 School of Biological Sciences, Monash University, Clayton, VIC 3800,
Australia
3 Institut für Biologie II, Zellbiologie, Universität Freiburg, 79104
Freiburg, Germany
Author for correspondence (e-mail:
schwarzs{at}mpiz-koeln.mpg.de)
Accepted 1 April 2004
STYLOSA (STY) in Antirrhinum and LEUNIG (LUG) in Arabidopsis control the spatially correct expression of homeotic functions involved in the control of floral organ identity. We show here that the sty mutant also displays alteration in leaf venation patterns and hypersensitivity towards auxin and polar auxin transport inhibitors, demonstrating that STY has a more general role in plant development. STY and LUG are shown to be orthologues that encode proteins with structural relation to GRO/TUP1-like co-repressors. Using a yeast-based screen we found that STY interacts with several transcription factors, suggesting that STY, like GRO/TUP1, forms complexes in vivo. Proteins of the YABBY family, characterised by containing a partial HMG domain, represent a major group of such interactors. In vivo association of STY with one of the YABBY proteins, GRAMINIFOLIA (GRAM), is supported by enhanced phenotypic defects in sty gram double mutants, for instance in the control of phyllotaxis, floral homeotic functions and organ polarity. Accordingly, the STY and GRAM protein and mRNA expression patterns overlap in emerging lateral organ primordia. STY is expressed in all meristems and later becomes confined to the adaxial domain and (pro)vascular tissue. This pattern is similar to genes that promote adaxial identity, and, indeed, STY expression follows, although does not control, adaxial fate. We discuss the complex roles of STY and GRAM proteins in reproductive and vegetative development, performed in part in physical association but also independently.
Key words: GRO/TUP1, Co-repressor, Floral organ identity, Leaf development, Auxin
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati
Twitter What's this?
This article has been cited by other articles:
![]() |
A. Y. Husbands, D. H. Chitwood, Y. Plavskin, and M. C.P. Timmermans Signals and prepatterns: new insights into organ polarity in plants Genes & Dev., September 1, 2009; 23(17): 1986 - 1997. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Sitaraman, M. Bui, and Z. Liu LEUNIG_HOMOLOG and LEUNIG Perform Partially Redundant Functions during Arabidopsis Embryo and Floral Development Plant Physiology, June 1, 2008; 147(2): 672 - 681. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Goldshmidt, J. P. Alvarez, J. L. Bowman, and Y. Eshed Signals Derived from YABBY Gene Activities in Organ Primordia Regulate Growth and Partitioning of Arabidopsis Shoot Apical Meristems PLANT CELL, May 1, 2008; 20(5): 1217 - 1230. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Azhakanandam, S. Nole-Wilson, F. Bao, and R. G. Franks SEUSS and AINTEGUMENTA Mediate Patterning and Ovule Initiation during Gynoecium Medial Domain Development Plant Physiology, March 1, 2008; 146(3): 1165 - 1181. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Gonzalez, A. J. Bowen, T. S. Carroll, and R. S. Conlan The Transcription Corepressor LEUNIG Interacts with the Histone Deacetylase HDA19 and Mediator Components MED14 (SWP) and CDK8 (HEN3) To Repress Transcription Mol. Cell. Biol., August 1, 2007; 27(15): 5306 - 5315. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. M. Ha, J. H. Jun, H. G. Nam, and J. C. Fletcher BLADE-ON-PETIOLE1 and 2 Control Arabidopsis Lateral Organ Fate through Regulation of LOB Domain and Adaxial-Abaxial Polarity Genes PLANT CELL, June 1, 2007; 19(6): 1809 - 1825. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. R. Yadav, K. Prasad, and U. Vijayraghavan Divergent Regulatory OsMADS2 Functions Control Size, Shape and Differentiation of the Highly Derived Rice Floret Second-Whorl Organ Genetics, May 1, 2007; 176(1): 283 - 294. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Balanza, M. Navarrete, M. Trigueros, and C. Ferrandiz Patterning the female side of Arabidopsis: the importance of hormones J. Exp. Bot., October 1, 2006; 57(13): 3457 - 3469. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. V. Sridhar, A. Surendrarao, and Z. Liu APETALA1 and SEPALLATA3 interact with SEUSS to mediate transcription repression during flower development Development, August 15, 2006; 133(16): 3159 - 3166. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Nole-Wilson and B. A. Krizek AINTEGUMENTA Contributes to Organ Polarity and Regulates Growth of Lateral Organs in Combination with YABBY Genes Plant Physiology, July 1, 2006; 141(3): 977 - 987. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. F. Golz, M. Roccaro, R. Kuzoff, and A. Hudson GRAMINIFOLIA promotes growth and polarity of Antirrhinum leaves Development, August 1, 2004; 131(15): 3661 - 3670. [Abstract] [Full Text] [PDF] |
||||