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Series GSE18808 Query DataSets for GSE18808
Status Public on Aug 24, 2010
Title A methyl transferase links the circadian clock to the regulation of alternative splicing
Organisms Arabidopsis thaliana; Drosophila melanogaster
Experiment type Expression profiling by array
Expression profiling by genome tiling array
Summary Study on differential gene expression and splicing between wildtype and clock mutants. This study is part of a comparative analysis of the role of Protein Methyltransferase 5 in the regulation of transcriptional and post-transcriptional processes simultaneously in Arabidopsis and Drosophila.
Circadian rhythms allow organisms to time biological processes to the most appropriate phases of the day/night cycle1. Post-transcriptional regulation is emerging as an important component of circadian networks2-6, but the molecular mechanisms linking the circadian clock to the control of RNA processing are largely unknown. Here we show that Protein Arginine Methyl Transferase 5 (PRMT5), which transfers methyl groups to arginine residues present in histones7 and Sm spliceosomal proteins8,9, links the circadian clock to the control of alternative splicing in plants. Mutations in prmt5impair multiple circadian rhythms in Arabidopsis thaliana and this phenotype is caused, at least in part, by a strong alteration in alternative splicing of the core-clock gene PSEUDO RESPONSE REGULATOR 9 (PRR9). Furthermore, genome wide studies show that PRMT5 contributes to regulate many pre-mRNA splicing events most likely modulating 5´splice site (5´ss) recognition. PRMT5 expression shows daily and circadian oscillations, and this contributes to mediate the circadian regulation of expression and alternative splicing of a subset of genes. Circadian rhythms in locomotor activity are also disrupted in dart5, a mutant affected in the Drosophila melanogaster PRMT5 homolog, and this is associated with alterations in splicing of the core-clock gene period (per) and several clock associated genes. Our results reveal a key role for PRMT5 in the regulation of alternative splicing and indicate that the interplay between the circadian clock and the regulation of alternative splicing by PRMT5 constitutes a common mechanism that helps organisms to synchronize physiological processes with daily changes in environmental conditions.
 
Overall design Each genotype has three replicates, Single channel. Two species, each with wildtype and mutant.
For the gene expression Samples (GSM586328-33): Wild type (WT) plants and prmt5-5 mutant plants were grown under continuous white light for three weeks, at 22 degrees centigrades. Total RNA extracted from aerial tissue was used for microarray analysis.
 
Contributor(s) Sanchez SE, Petrillo E, Beckwith EJ, Zhang X, Rugnone ML, Hernando CE, Cuevas JC, Godoy Herz MA, Depetris-Chauvin A, Simpson CG, Brown JW, Cerdán PD, Borevitz JO, Mas P, Ceriani MF, Kornblihtt AR, Yanovsky MJ
Citation(s) 20962777
Submission date Aug 24, 2010
Last update date Jun 12, 2017
Contact name Marcelo Javier Yanovsky
E-mail(s) yanovsky@agro.uba.ar
Phone 5411 4524-8070
Fax 5411 4514-8730
Organization name IFEVA
Department Applied Biology
Lab Chronobiology
Street address Av. San Martín 4453
City Buenos Aires
State/province Capital Federal
ZIP/Postal code 1417
Country Argentina
 
Platforms (3)
GPL198 [ATH1-121501] Affymetrix Arabidopsis ATH1 Genome Array
GPL1979 AtTile1F to Arabidopsis Tiling 1.0F
GPL6882 Affymetrix Drosophila Genome Tiling Array 1.0F (Dm35b_MF_v02)
Samples (18)
GSM466433 At_wildtype_rep1
GSM466447 At_wildtype_rep2
GSM466454 At_wildtype_rep3
Relations
BioProject PRJNA121225

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
GSE18808_RAW.tar 360.1 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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