Transcriptomics

Dataset Information

67

Transcription profiling by array of Arabidopsis mutant for scm, cpc, or wer and myb23 after salt stress treatment


ABSTRACT: We performed an expression analysis of the response of seedling root tips to 1 hour of treatment with 140mM NaCl using mutants defective in root hair patterning. Cells are amazingly adept at integrating both external and internal cues to regulate transcriptional states. While internal processes such as differentiation and cell-type specification are generally understood to have an important impact on gene expression, very little is known about how cells utilize these developmental cues to regulate responses to external stimuli. Here we use the response to a well characterized environmental stress, high salinity, to obtain a global view of the role that cell identity plays in guiding transcriptional responses in the root of Arabidopsis. Our analysis is based on three microarray data sets we have generated that explore transcriptional changes spatially among 6 cell layers and 4 longitudinal regions or temporally along 5 time points after salt treatment. We show that the majority of the response to salt stress is cell-type specific resulting in the differential regulation of unique biological functions in subsets of cell layers. To understand the regulatory mechanisms controlling these responses we have analyzed cis-element enrichment in the promoters of salt responsive genes and demonstrate that known stress regulatory elements likely control responses to salt occurring in multiple cell types. Despite the extensive shift in transcriptional state that salt stress elicits, we are able to identify several biological processes that consistently define each cell layer and find that transcriptional regulators of cell-identity tend to exhibit robust cell-type specific expression. Finally, using mutants that disrupt cell-type specification in the epidermis, we reveal cell autonomous and non-autonomous effects when cell identity is altered. Together, these data elucidate a novel intersection between physiology and development and expand our understanding of how transcriptional states are regulated in a multi-cellular context. Experiment Overall Design: Seedlings were grown for 5 days before being transferred to standard media or media supplemented with 140mM NaCl. One hour after transfer, a razor blade was used to cut the root ~5 mm above the root tip. Approximately 30 roots were pooled per replicate. Two biological replicates were performed per genotype, per condition.

OTHER RELATED OMICS DATASETS IN: E-GEOD-10496E-GEOD-7641

INSTRUMENT(S): 418 [Affymetrix]

ORGANISM(S): Arabidopsis thaliana  

SUBMITTER: Jose Ramon Dinneny  

PROVIDER: E-GEOD-8787 | ArrayExpress | 2008-06-16

SECONDARY ACCESSION(S): GSE8787PRJNA102085

REPOSITORIES: GEO, ArrayExpress

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Publications

Cell identity mediates the response of Arabidopsis roots to abiotic stress.

Dinneny José R JR   Long Terri A TA   Wang Jean Y JY   Jung Jee W JW   Mace Daniel D   Pointer Solomon S   Barron Christa C   Brady Siobhan M SM   Schiefelbein John J   Benfey Philip N PN  

Science (New York, N.Y.) 20080424 5878


Little is known about the way developmental cues affect how cells interpret their environment. We characterized the transcriptional response to high salinity of different cell layers and developmental stages of the Arabidopsis root and found that transcriptional responses are highly constrained by developmental parameters. These transcriptional changes lead to the differential regulation of specific biological functions in subsets of cell layers, several of which correspond to observable physiol  ...[more]

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