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1.
Plant J ; 109(6): 1386-1396, 2022 03.
Article in English | MEDLINE | ID: mdl-34919778

ABSTRACT

Extracellular ATP (eATP) is known to act as a danger signal in both plants and animals. In plants, eATP is recognized by the plasma membrane (PM)-localized receptor P2K1 (LecRK-I.9). Among the first measurable responses to eATP addition is a rapid rise in cytoplasmic free calcium levels ([Ca2+ ]cyt ), which requires P2K1. However, the specific transporter/channel proteins that mediate this rise in [Ca2+ ]cyt are unknown. Through a forward genetic screen, we identified an Arabidopsis ethylmethanesulfonate (EMS) mutant impaired in the [Ca2+ ]cyt response to eATP. Positional cloning revealed that the mutation resided in the cngc6 gene, which encodes cyclic nucleotide-gated ion channel 6 (CNGC6). Mutation of the CNGC6 gene led to a notable decrease in the PM inward Ca2+ current in response to eATP. eATP-induced mitogen-activated protein kinase activation and gene expression were also significantly lower in cngc6 mutant plants. In addition, cngc6 mutant plants were also more susceptible to the bacterial pathogen Pseudomonas syringae. Taken together, our results indicate that CNGC6 plays a crucial role in mediating eATP-induced [Ca2+ ]cyt signaling, as well as plant immunity.


Subject(s)
Arabidopsis Proteins , Arabidopsis , Cyclic Nucleotide-Gated Cation Channels , Adenosine Triphosphate/metabolism , Arabidopsis/genetics , Arabidopsis/metabolism , Arabidopsis Proteins/genetics , Arabidopsis Proteins/metabolism , Calcium/metabolism , Cyclic Nucleotide-Gated Cation Channels/genetics , Cyclic Nucleotide-Gated Cation Channels/metabolism , Nucleotides, Cyclic , Plant Immunity/genetics
2.
Curr Protoc Plant Biol ; 1(2): 285-291, 2016 Mar.
Article in English | MEDLINE | ID: mdl-30775859

ABSTRACT

Transient gene expression in protoplasts provides a powerful tool to study protein expression, protein localization, protein-protein association, and gene expression regulation, etc. There are several methods including electroporation, which have been reported to introduce DNA into protoplasts. However, one of the best methods used is polyethylene glycol (PEG)-mediated transfection. Here, we describe an improved PEG-mediated transformation method including preparation of protoplasts, PEG-mediated transformation, and, by way of example, expression of the AtLYK5 gene (AT2G33580) in protoplasts. The protoplast transient expression system provides unique capabilities to support cell-based experiments involved in plant biochemistry and physiology. © 2016 by John Wiley & Sons, Inc.

3.
J Exp Bot ; 66(19): 5727-38, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26049159

ABSTRACT

Although lipo-chitooligosaccharides (LCOs) are important signal molecules for plant-symbiont interactions, a number of reports suggest that LCOs can directly impact plant growth and development, separate from any role in plant symbioses. In order to investigate this more closely, maize and Setaria seedlings were treated with LCO and their growth was evaluated. The data indicate that LCO treatment significantly enhanced root growth. RNA-seq transcriptomic analysis of LCO-treated maize roots identified a number of genes whose expression was significantly affected by the treatment. Among these genes, some LCO-up-regulated genes are likely involved in root growth promotion. Interestingly, some stress-related genes were down-regulated after LCO treatment, which might indicate reallocation of resources from defense responses to plant growth. The promoter activity of several LCO-up-regulated genes using a ß-glucuronidase reporter system was further analysed. The results showed that the promoters were activated by LCO treatment. The data indicate that LCO can directly impact maize root growth and gene expression.


Subject(s)
Chitin/analogs & derivatives , Poaceae/growth & development , Signal Transduction , Carbon/chemistry , Chitin/pharmacology , Chitosan , Gene Expression Regulation, Plant/drug effects , Lipopolysaccharides/pharmacology , Oligosaccharides , Poaceae/chemistry , Poaceae/drug effects , Poaceae/metabolism , Seedlings/chemistry , Seedlings/drug effects , Seedlings/growth & development , Seedlings/metabolism , Sequence Analysis, RNA , Signal Transduction/drug effects , Transcriptome/drug effects , Zea mays/chemistry , Zea mays/drug effects , Zea mays/growth & development , Zea mays/metabolism
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