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Toward the identification and regulation of the Arabidopsis thaliana ABI3 regulon.


ABSTRACT: The plant-specific, B3 domain-containing transcription factor ABSCISIC ACID INSENSITIVE3 (ABI3) is an essential component of the regulatory network controlling the development and maturation of the Arabidopsis thaliana seed. Genome-wide chromatin immunoprecipitation (ChIP-chip), transcriptome analysis, quantitative reverse transcriptase-polymerase chain reaction and a transient promoter activation assay have been combined to identify a set of 98 ABI3 target genes. Most of these presumptive ABI3 targets require the presence of abscisic acid for their activation and are specifically expressed during seed maturation. ABI3 target promoters are enriched for G-box-like and RY-like elements. The general occurrence of these cis motifs in non-ABI3 target promoters suggests the existence of as yet unidentified regulatory signals, some of which may be associated with epigenetic control. Several members of the ABI3 regulon are also regulated by other transcription factors, including the seed-specific, B3 domain-containing FUS3 and LEC2. The data strengthen and extend the notion that ABI3 is essential for the protection of embryonic structures from desiccation and raise pertinent questions regarding the specificity of promoter recognition.

SUBMITTER: Monke G 

PROVIDER: S-EPMC3458547 | biostudies-literature | 2012 Sep

REPOSITORIES: biostudies-literature

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Toward the identification and regulation of the Arabidopsis thaliana ABI3 regulon.

Mönke Gudrun G   Seifert Michael M   Keilwagen Jens J   Mohr Michaela M   Grosse Ivo I   Hähnel Urs U   Junker Astrid A   Weisshaar Bernd B   Conrad Udo U   Bäumlein Helmut H   Altschmied Lothar L  

Nucleic acids research 20120622 17


The plant-specific, B3 domain-containing transcription factor ABSCISIC ACID INSENSITIVE3 (ABI3) is an essential component of the regulatory network controlling the development and maturation of the Arabidopsis thaliana seed. Genome-wide chromatin immunoprecipitation (ChIP-chip), transcriptome analysis, quantitative reverse transcriptase-polymerase chain reaction and a transient promoter activation assay have been combined to identify a set of 98 ABI3 target genes. Most of these presumptive ABI3  ...[more]

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