Delayed flowering time in Arabidopsis and Brassica rapa by the overexpression of FLOWERING LOCUS C (FLC) homologs isolated from Chinese cabbage (Brassica rapa L. ssp pekinensis)

被引:103
作者
Kim, Soo-Yun [1 ]
Park, Beom-Seok [1 ]
Kwon, Soo-Jin [1 ]
Kim, Jungsun [1 ]
Lim, Myung-Ho [1 ]
Park, Young-Doo [1 ]
Kim, Dool Yi [1 ]
Suh, Seok-Chul [1 ]
Jin, Yong-Moon [1 ]
Ahn, Ji Hoon [1 ]
Lee, Yeon-Hee [1 ]
机构
[1] RDA, Natl Inst Agr Biotechnol, Suwon 441707, South Korea
关键词
Chinese cabbage; flowering time; transcript level; transgenic plants;
D O I
10.1007/s00299-006-0243-1
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Chinese cabbage plants remain in the vegetative growth phase until they have experienced prolonged exposure to cold temperature, known as vernalization. This inhibition of flowering is caused by the high levels of FLOWERING LOCUS C (FLC) expression. To increase the product value of Chinese cabbage by inhibiting the floral transition, three genes (BrFLC1, BrFLC2, and BrFLC3) homologous to the AtFLC gene, which encodes a floral repressor, were isolated from the Chinese cabbage 'Chiifu'. These genes showed high similarity to AtFLC, although the putative BrFLC1 protein contained ten more residues than AtFLC. The BrFLC genes were expressed ubiquitously, except that BrFLC3 was not expressed in roots. BrFLC1 and BrFLC2 showed stronger expression than BrFLC3 in unvernalized and vernalized Chinese cabbage. The expression levels of the three BrFLC genes were lower in an early-flowering Chinese cabbage, suggesting that the BrFLC transcript level was associated with flowering time. Constitutive expression of the BrFLC genes in Arabidopsis significantly delayed flowering, which was also observed in transgenic Chinese cabbage overexpressing BrFLC3. These results suggest that the BrFLC genes act similarly to AtFLC. Our results provide a technique for controlling flowering time in Chinese cabbage and other crops to produce high yields of vegetative tissues.
引用
收藏
页码:327 / 336
页数:10
相关论文
共 25 条
[1]   Multiple pathways in the decision to flower: Enabling, promoting, and resetting [J].
Boss, PK ;
Bastow, RM ;
Mylne, JS ;
Dean, C .
PLANT CELL, 2004, 16 (SUPPL.) :S18-S31
[2]   GENOMIC SEQUENCING [J].
CHURCH, GM ;
GILBERT, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07) :1991-1995
[3]  
GORDON G, 1999, ANNU REV CELL DEV BI, V99, P519
[4]   Role of chromatin modification in flowering-time control [J].
He, YH ;
Amasino, RM .
TRENDS IN PLANT SCIENCE, 2005, 10 (01) :30-35
[5]   Antagonistic regulation of flowering-time gene SOC1 by CONSTANS and FLC via separate promoter motifs [J].
Hepworth, SR ;
Valverde, F ;
Ravenscroft, D ;
Mouradov, A ;
Coupland, G .
EMBO JOURNAL, 2002, 21 (16) :4327-4337
[6]   Molecular and genetic mechanisms of floral control [J].
Jack, T .
PLANT CELL, 2004, 16 :S1-S17
[7]   Molecular analysis of FRIGIDA, a major determinant of natural variation in Arabidopsis flowering time [J].
Johanson, U ;
West, J ;
Lister, C ;
Michaels, S ;
Amasino, R ;
Dean, C .
SCIENCE, 2000, 290 (5490) :344-347
[8]   The AGAMOUS-LIKE 20 MADS domain protein integrates floral inductive pathways in Arabidopsis [J].
Lee, H ;
Suh, SS ;
Park, E ;
Cho, E ;
Ahn, JH ;
Kim, SG ;
Lee, JS ;
Kwon, YM ;
Lee, I .
GENES & DEVELOPMENT, 2000, 14 (18) :2366-2376
[9]   EFFECT OF VERNALIZATION, PHOTOPERIOD, AND LIGHT QUALITY ON THE FLOWERING PHENOTYPE OF ARABIDOPSIS PLANTS CONTAINING THE FRIGIDA GENE [J].
LEE, I ;
AMASINO, RM .
PLANT PHYSIOLOGY, 1995, 108 (01) :157-162
[10]  
LEE YH, 2000, J PLANT BIOTECHNOL, V2, P35