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Global Analysis of DELLA Direct Targets in Early Gibberellin Signaling inArabidopsis

生物 染色质免疫沉淀 赤霉素 抑制因子 拟南芥 转录因子 信号转导 细胞生物学 F盒蛋白 转录调控 发起人 泛素 脱落酸 基因表达调控 基因 泛素连接酶 基因表达 遗传学 突变体
作者
Rodolfo Zentella,Zhonglin Zhang,Me‐Hea Park,Stephen G. Thomas,Akira Endo,Kohji Murase,Christine M. Fleet,Yusuke Jikumaru,Eiji Nambara,Yuji Kamiya,Tai‐ping Sun
出处
期刊:The Plant Cell [Oxford University Press]
卷期号:19 (10): 3037-3057 被引量:627
标识
DOI:10.1105/tpc.107.054999
摘要

Bioactive gibberellins (GAs) are phytohormones that regulate growth and development throughout the life cycle of plants. DELLA proteins are conserved growth repressors that modulate all aspects of GA responses. These GA-signaling repressors are nuclear localized and likely function as transcriptional regulators. Recent studies demonstrated that GA, upon binding to its receptor, derepresses its signaling pathway by binding directly to DELLA proteins and targeting them for rapid degradation via the ubiquitin-proteasome pathway. Therefore, elucidating the signaling events immediately downstream of DELLA is key to our understanding of how GA controls plant development. Two sets of microarray studies followed by quantitative RT-PCR analysis allowed us to identify 14 early GA-responsive genes that are also early DELLA-responsive in Arabidopsis thaliana seedlings. Chromatin immunoprecipitation provided evidence for in vivo association of DELLA with promoters of eight of these putative DELLA target genes. Expression of all 14 genes was downregulated by GA and upregulated by DELLA. Our study reveals that DELLA proteins play two important roles in GA signaling: (1) they help establish GA homeostasis by direct feedback regulation on the expression of GA biosynthetic and GA receptor genes, and (2) they promote the expression of downstream negative components that are putative transcription factors/regulators or ubiquitin E2/E3 enzymes. In addition, one of the putative DELLA targets, XERICO, promotes accumulation of abscisic acid (ABA) that antagonizes GA effects. Therefore, DELLA may restrict GA-promoted processes by modulating both GA and ABA pathways.
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