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Updated: Aug 11, 2026

Investigating Tissue- and Organ-specific Phytochrome Responses using FACS-assisted Cell-type Specific Expression Profiling in Arabidopsis thaliana
Published on: May 29, 2010
The early dark-response in Arabidopsis thaliana revealed by cDNA microarray analysis
Byung-Hoon Kim1, Albrecht G von Arnim
1Department of Biochemistry, Cellular and Molecular Biology, The University of Tennessee, Knoxville, TN 37996-0840, USA.
Plants rapidly adjust to darkness by activating hundreds of genes involved in diverse cellular processes. This early dark response is distinct from long-term adaptation and involves abscisic acid signaling.
Area of Science:
- Plant molecular biology
- Transcriptomics
- Plant physiology
Background:
- Light responses are crucial for plant development, but the immediate effects of darkness are less understood.
- Circadian rhythms can influence plant responses to light and dark cycles.
Purpose of the Study:
- To characterize the early transcriptional changes in Arabidopsis thaliana seedlings shifting from light to darkness.
- To differentiate the early dark response from long-term dark adaptation and etiolation.
Main Methods:
- Transcriptome analysis of Arabidopsis thaliana seedling leaves after 1-8 hours in darkness.
- Gene expression clustering and gene ontology analysis.
- Bioinformatic comparison with existing microarray data.
Main Results:
- Approximately 790 genes showed altered expression in response to darkness.
- The early dark response comprises distinct transient, sustained, and late clusters.
- COP1 (constitutive photomorphogenic 1) is not a primary regulator of the early dark response.
- Abscisic acid (ABA) signaling is implicated in the early dark response, independent of ABA level changes.
Conclusions:
- The early response to darkness in plants is a complex, multi-phased process.
- This response is partially distinct from the inverse of light responses and sugar deprivation effects.
- Abscisic acid signaling plays a significant role in early dark adaptation, suggesting interactions with sugar and redox signaling pathways.
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