CUPULIFORMIS establishes lateral organ boundaries in Antirrhinum

被引:149
作者
Weir, I
Lu, JP
Cook, H
Causier, B
Schwarz-Sommer, Z
Davies, B [1 ]
机构
[1] Univ Leeds, Ctr Plant Sci, Leeds LS2 9JT, W Yorkshire, England
[2] Max Planck Inst Zuchtungsforsch, D-50829 Cologne, Germany
来源
DEVELOPMENT | 2004年 / 131卷 / 04期
基金
英国生物技术与生命科学研究理事会;
关键词
Antirrhinum; Arabidopsis; boundaries; medstems; transcription factors;
D O I
10.1242/dev.00993
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cupuliformis mutants are defective in shoot apical meristern formation, but cup plants overcome this early barrier to development to reach maturity. CUP encodes a NAG domain transcription factor, homologous to the Petunia NAM and Arabidopsis CUC proteins. The phenotype of cup mutants differs from those of nam and cuc1 cuc2 in that dramatic organ fusion is observed throughout development. In addition to cotyledon and floral organ fusions, severe lateral organ fusion is found in leaves and inflorescences, and the apical meristem becomes highly fasciated. These features reveal a role for CUP in the establishment of all above ground organ boundaries. Consistent with this function, CUP is expressed at the boundaries of all lateral organs and meristems. It is not currently known how NAC-domain genes act to establish organ boundaries. Here, we show that CUP directly interacts with a TCP-domain transcription factor. Members of the TCP-domain family have previously been shown to regulate organ outgrowth. Our results suggest a model for the establishment of organ boundaries based on the localised expression of NAC-domain and TCP-domain factors.
引用
收藏
页码:915 / 922
页数:8
相关论文
共 31 条
[1]   Genes involved in organ separation in Arabidopsis: An analysis of the cup-shaped cotyledon mutant [J].
Aida, M ;
Ishida, T ;
Fukaki, H ;
Fujisawa, H ;
Tasaka, M .
PLANT CELL, 1997, 9 (06) :841-857
[2]  
Aida M, 1999, DEVELOPMENT, V126, P1563
[3]  
BARTEL P, 1993, BIOTECHNIQUES, V14, P920
[4]   Phyllotactic pattern and stem cell fate are determined by the Arabidopsis homeobox gene BELLRINGER [J].
Byrne, ME ;
Groover, AT ;
Fontana, JR ;
Martienssen, RA .
DEVELOPMENT, 2003, 130 (17) :3941-3950
[5]   Control of flower development and phyllotaxy by meristem identity genes in Antirrhinum [J].
Carpenter, R ;
Copsey, L ;
Vincent, C ;
Doyle, S ;
Magrath, R ;
Coen, E .
PLANT CELL, 1995, 7 (12) :2001-2011
[6]   An Antirrhinum ternary complex factor specifically interacts with C-function and SEPALLATA-like MADS-box factors [J].
Causier, B ;
Cook, H ;
Davies, B .
PLANT MOLECULAR BIOLOGY, 2003, 52 (05) :1051-1062
[7]   The TCP domain: a motif found in proteins regulating plant growth and development [J].
Cubas, P ;
Lauter, N ;
Doebley, J ;
Coen, E .
PLANT JOURNAL, 1999, 18 (02) :215-222
[8]   The CUP-SHAPED COTYLEDON genes promote adventitious shoot formation on calli [J].
Daimon, Y ;
Takabe, K ;
Tasaka, M .
PLANT AND CELL PHYSIOLOGY, 2003, 44 (02) :113-121
[9]   Multiple interactions amongst floral homeotic MADS box proteins [J].
Davies, B ;
EgeaCortines, M ;
Silva, ED ;
Saedler, H ;
Sommer, H .
EMBO JOURNAL, 1996, 15 (16) :4330-4343
[10]   The evolution of apical dominance in maize [J].
Doebley, J ;
Stec, A ;
Hubbard, L .
NATURE, 1997, 386 (6624) :485-488