The Single-Stranded DNA-Binding Protein WHIRLY1 Represses WRKY53 Expression and Delays Leaf Senescence in a Developmental Stage-Dependent Manner in Arabidopsis
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作者:
Miao, Ying
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Fujian Agr & Forestry Univ, Coll Life Sci, Ctr Mol Cell & Syst Biol, Fuzhou 350003, Peoples R China
Univ Tubingen, Dept Gen Genet, Ctr Plant Mol Biol, D-72076 Tubingen, Germany
Univ Kiel, Inst Bot, D-24118 Kiel, GermanyFujian Agr & Forestry Univ, Coll Life Sci, Ctr Mol Cell & Syst Biol, Fuzhou 350003, Peoples R China
Miao, Ying
[1
,2
,3
]
Jiang, Jingjing
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Univ Tubingen, Dept Gen Genet, Ctr Plant Mol Biol, D-72076 Tubingen, GermanyFujian Agr & Forestry Univ, Coll Life Sci, Ctr Mol Cell & Syst Biol, Fuzhou 350003, Peoples R China
Jiang, Jingjing
[2
]
Ren, Yujun
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Fujian Agr & Forestry Univ, Coll Life Sci, Ctr Mol Cell & Syst Biol, Fuzhou 350003, Peoples R ChinaFujian Agr & Forestry Univ, Coll Life Sci, Ctr Mol Cell & Syst Biol, Fuzhou 350003, Peoples R China
Ren, Yujun
[1
]
Zhao, Ziwei
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Univ Kiel, Inst Bot, D-24118 Kiel, GermanyFujian Agr & Forestry Univ, Coll Life Sci, Ctr Mol Cell & Syst Biol, Fuzhou 350003, Peoples R China
Zhao, Ziwei
[3
]
机构:
[1] Fujian Agr & Forestry Univ, Coll Life Sci, Ctr Mol Cell & Syst Biol, Fuzhou 350003, Peoples R China
Leaf senescence in plants involves both positive and negative transcriptional regulation. In this work, we show evidence for the single-stranded DNA-binding protein WHIRLY1 (WHY1) that functions as an upstream suppressor of WRKY53 in a developmental stage-dependent manner during leaf senescence in Arabidopsis (Arabidopsis thaliana). The why1 mutant displayed an early-senescence phenotype. In this background, the expression levels of both WRKY53 and the senescence-associated protease gene SAG12 increased. WHY1 bound to the sequence region that contains an elicitor response element motif-like sequence, GNNNAAATT, plus an AT-rich telomeric repeat-like sequence in the WRKY53 promoter in in vivo and in vitro mutagenesis assays as well as in a chromatin immunoprecipitation assay. This binding to the promoter of WRKY53 was regulated in a developmental stage-dependent manner, as verified by chromatin immunoprecipitation-polymerase chain reaction assay. This direct interaction was further determined by a transient expression assay in which WHY1 repressed beta-GLUCURONIDASE gene expression driven by the WRKY53 promoter. Genetic analysis of double mutant transgenic plants revealed that WHY1 overexpression in the wrky53 mutant (oeWHY1wrky53) had no effect on the stay-green phenotype of the wrky53 mutant, while a WHY1 knockout mutant in the wrky53 mutant background (why1wrky53) generated subtle change in the leaf yellow/green phenotype. These results suggest that WHY1 was an upstream regulator of WRKY53 during leaf senescence.
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页码:746 / 756
页数:11
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