Integrating long-day flowering signals: a LEAFY binding site is essential for proper photoperiodic activation of APETALA1

被引:58
作者
Benlloch, Reyes [1 ,2 ,3 ,4 ,5 ]
Kim, Min Chul [6 ]
Sayou, Camille [1 ,2 ,3 ,5 ]
Thevenon, Emmanuel [1 ,2 ,3 ,5 ]
Parcy, Francois [1 ,2 ,3 ,5 ]
Nilsson, Ove [4 ]
机构
[1] CEA, iRTSV, Lab Physiol Cellulaire & Vegetale, F-38054 Grenoble, France
[2] CNRS, UMR5168, F-38054 Grenoble, France
[3] Univ Grenoble 1, UMR5168, F-38041 Grenoble, France
[4] Swedish Univ Agr Sci, Umea Plant Sci Ctr, Dept Forest Genet & Plant Physiol, S-90183 Umea, Sweden
[5] INRA, UMR1200, F-38054 Grenoble, France
[6] Gyeongsang Natl Univ, Plant Mol Biol & Biotechnol Res Ctr, Program BK21, Div Appl Life Sci, Jinju 660701, South Korea
基金
英国生物技术与生命科学研究理事会; 瑞典研究理事会;
关键词
APETALA1; LEAFY; FLOWERING LOCUS T; FLOWERING LOCUS D; floral induction; photoperiod; FLORAL HOMEOTIC GENE; TRANSCRIPTION FACTOR; ARABIDOPSIS-THALIANA; DNA-BINDING; MOLECULAR CHARACTERIZATION; MERISTEM FATE; TARGET GENES; TIME GENES; PATHWAY; EXPRESSION;
D O I
10.1111/j.1365-313X.2011.04660.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The transition to flowering in Arabidopsis is characterized by the sharp and localized upregulation of APETALA1 (AP1) transcription in the newly formed floral primordia. Both the flower meristem-identity gene LEAFY (LFY) and the photoperiod pathway involving the FLOWERING LOCUS T (FT) and FD genes contribute to this upregulation. These pathways have been proposed to act independently but their respective contributions and mode of interaction have remained elusive. To address these questions, we studied the AP1 regulatory region. Combining in vitro and in vivo approaches, we identified which of the three putative LFY binding sites present in the AP1 promoter is essential for its activation by LFY. Interestingly, we found that this site is also important for the correct photoperiodic-dependent upregulation of AP1. In contrast, a previously proposed putative FD-binding site appears dispensable and unable to bind FD and we found no evidence for FD binding to other sites in the AP1 promoter, suggesting that the FT/FD-dependent activation of AP1 might be indirect. Altogether, our data give new insight into the interaction between the FT and LFY pathways in the upregulation of AP1 transcription under long-day conditions.
引用
收藏
页码:1094 / 1102
页数:9
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