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Series GSE39746 Query DataSets for GSE39746
Status Public on Sep 10, 2012
Title Argonaute proteins couple chromatin silencing to alternative splicing (exon array)
Organism Mus musculus
Experiment type Expression profiling by array
Summary While Argonaute (AGO) proteins play a major role in transcriptional gene silencing (TGS) in many organisms, their role in the nucleus of somatic mammalian cells remains elusive. Here, we have purified AGO1 and AGO2 chromatin-embedded complexes, and found these proteins associated with previously described partners, but also with chromatin modifiers and, rather unexpectedly, with different splicing factors. Using the CD44 gene as a model for alternative splicing, we show that both AGO1 and AGO2 are required for Protein Kinase C (PKC)-dependent variant exon inclusion. AGO proteins facilitate the spliceosome recruitment and modulate the elongation rate of RNA polymerase II (RNAPII). The recruitment of AGO proteins to CD44 transcribed region is dependent on both the endonuclease Dicer and the chromodomain-containing protein HP1g, and results in locally increased levels of histone H3 lysine 9 (H3K9) methylation on variant exons. Genome wide analysis of splicing in either AGO2 or Dicer null cells showed that the two proteins have similar effects on many splicing events. Finally, sRNAs associated with nuclear AGO2 are mostly in sense orientation relative to protein-coding genes, supporting a role for intragenic antisense non-coding RNAs in the recruitment AGO and splicing factors. Together, our data demonstrate for the first time that the endogenous RNAi pathway is involved in alternative splicing decisions, unravelling a new model in which AGO proteins couple RNAPII elongation and chromatin modification.
Study of AGO2 or Dicer knock-out on gene expression and splicing regulation in MEF cells
 
Overall design Transcriptome analysis of AGO2 and Dicer null MEF cells on GeneChip® Mouse Exon 1.0 ST Arrays (Affymetrix). Dicer null MEF cells and wild-type MEF cells were from M. Otsuka. AGO2 null MEF cells were from A. Tarakhovsky. Experiment has been done in experimental triplicates. 9 Total samples were analyzed.
 
Contributor(s) Ameyar-Zazoua M, Muchardt C, Harel-Bellan A, Batsché E
Citation(s) 22961379
Submission date Jul 30, 2012
Last update date Mar 06, 2018
Contact name Eric Batsche
Phone (33)1 44 27 34 77
Organization name IBPS - Institut Biologie Paris Seine
Department B2A Biological Adaptation and Ageing - UMR8256 CNRS
Lab Epigenetics and RNA metabolism in human diseases
Street address 7-9, Quai Saint Bernard
City Paris
ZIP/Postal code 75006
Country France
 
Platforms (2)
GPL6096 [MoEx-1_0-st] Affymetrix Mouse Exon 1.0 ST Array [transcript (gene) version]
GPL6193 [MoEx-1_0-st] Affymetrix Mouse Exon 1.0 ST Array [probe set (exon) version]
Samples (18)
GSM978467 array1 for AGO2 knock-out in MEF cells, biological (gene) rep1
GSM978468 array2 for AGO2 knock-out in MEF cells, biological (gene) rep2
GSM978469 array3 for AGO2 knock-out in MEF cells, biological (gene) rep3
This SubSeries is part of SuperSeries:
GSE39749 Argonaute proteins couple chromatin silencing to alternative splicing
Relations
BioProject PRJNA171691

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Supplementary file Size Download File type/resource
GSE39746_RAW.tar 410.6 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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