NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE7743 Query DataSets for GSE7743
Status Public on May 09, 2007
Title Genome-wide gene expression analysis reveals a critical role for CRY1 in the Response of Arabidopsis to High Irradiance
Organism Arabidopsis thaliana
Experiment type Expression profiling by array
Summary Exposure to high irradiance results in dramatic changes in nuclear gene expression in plants. However, little is known about the mechanisms by which changes in irradiance are sensed and how the information is transduced to the nucleus to initiate the genetic response. To investigate whether the photoreceptors are involved in the response to high irradiance, we analyzed expression of ELIP1, ELIP2, APX2 and LHCB2.4 in the phyA, phyB, cry1 and cry2 photoreceptor mutants and hy5 and hyh transcription factor mutants. Following exposure to high intensity white light for 3 h (HL, 1000 micro mol quanta m-2 s-1) expression of ELIP1/2 and APX2 was strongly induced and LHCB2.4 expression repressed in wild type. The cry1 and hy5 mutants showed specific mis-regulation of ELIP1/2 and we show that the induction of ELIP1/2 expression is mediated via CRY1 in a blue light intensity-dependent manner. Furthermore, using the Affymetrix Arabidopsis 24K Gene-Chip we showed that 77 of the HL responsive genes are regulated via CRY1, and 26 of those genes were also HY5 dependent. As a consequence of the mis-regulation of these genes the cry1 mutant displayed a high irradiance-sensitive phenotype with significant photoinactivation of PSII, indicated by reduced Fv/Fm. Thus, we describe a novel function of CRY1 in mediating plant responses to high irradiances that is essential to the induction of photoprotective mechanisms. This indicates that high irradiance can be sensed in a chloroplast-independent manner by a cytosolic/nucleic component.
Keywords: photoreceptor, transcription factor, cytosolic/nuclear component, chloroplast, stress response, photoprotection
 
Overall design All samples were done in biological triplicates (named A, B, C): Arabidopsis Col-O: growth conditions (7 d continuous white light; 100 micro mol quanta m-2 s-1, 22 °C), growth conditions followed by high light (3 hours 1000 micro mol quanta m-2 s-1, 22 °C) and growth conditions followed by blue light (3 hours; HQI-T 400 W lamps were filtered through color filter #74, 400-540 nm, absorption maximum: 470 nm (Night Blue; Rosco International))
cryptochrome 1 (cry1) mutant: growth conditions and growth conditions followed by 3 hours high light
long hypocotyl 5 (hy5) mutant: growth conditions and growth conditions followed by 3 hours high light
 
Contributor(s) Strand A, Kleine T, Kindgren P, Benedict C, Hendrickson L
Citation(s) 17478635
Submission date May 06, 2007
Last update date Aug 28, 2018
Contact name Tatjana Kleine
E-mail(s) tatjana.kleine@lmu.de
Organization name Ludwig-Maximilians-Universität München
Department Biologie I, Botanik
Lab Dario Leister
Street address Großhaderner Straße 2
City Planegg
ZIP/Postal code 82152
Country Germany
 
Platforms (1)
GPL198 [ATH1-121501] Affymetrix Arabidopsis ATH1 Genome Array
Samples (21)
GSM187239 Col-O_BL_A
GSM187240 Col-O_BL_B
GSM187241 Col-O_BL_C
Relations
Affiliated with GSE69995
BioProject PRJNA99855

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE7743_RAW.tar 94.2 Mb (http)(custom) TAR (of CEL, CHP)
Processed data provided as supplementary file

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap