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Series GSE243155 Query DataSets for GSE243155
Status Public on Jul 31, 2024
Title ARID3A coordinates the proliferation-differentiation switch of transit-amplifying cells in the intestine
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary Intestinal stem cells (ISCs) at the crypt base divide and give rise to progenitor cells that have the capacity to proliferate and differentiate into various mature epithelial cell types in the transit-amplifying (TA) zone. Here, we identified the transcription factor ARID3A as a novel regulator of intestinal epithelial cell proliferation and differentiation at the TA compartment. We show that ARID3A forms an expression gradient from villus tip to the early progenitors at the crypts mediated by TGF-β and WNT signalling. Intestinal epithelial-specific deletion of Arid3a reduces proliferation of TA cells. Bulk and single cell transcriptomic analysis shows increased enterocyte differentiation and reduced secretory cells in the Arid3a cKO intestine. Interestingly, upper-villus gene signatures of both enterocytes and secretory cells are enriched in the mutant intestine. We find that the enhanced enterocyte differentiation in the Arid3a cKO intestine is caused by increased binding of HNF1 and HNF4. Finally, we show that loss of Arid3a impairs irradiation-induced regenerative process by altering the dynamics of proliferation and apoptosis. Our findings imply that ARID3A may play a gatekeeping role in the TA compartment to maintain the “just-right” proliferation-to-differentiation ratio for tissue homeostasis and plasticity
 
Overall design Sorted single cell suspension from VillinCreERT2 (control) and VillinCreERT2, Arid3a fl/fl intestines. Two biological replicates per experimental condition were processed. Both Control and cKO animals were injected with tamoxifen at 8-10 weeks old and harvested at 1 month after the first injection.
 
Contributor(s) Angelis N, Baulies A, Boeing S
Citation(s) 39150450
Submission date Sep 13, 2023
Last update date Oct 08, 2024
Contact name Vivian Li
E-mail(s) vivian.li@crick.ac.uk
Organization name The Francis Crick Institute
Lab Stem Cell and Cancer Biology
Street address 1 Midland Road
City London
ZIP/Postal code NW1 1AT
Country United Kingdom
 
Platforms (1)
GPL24247 Illumina NovaSeq 6000 (Mus musculus)
Samples (3)
GSM7780016 VillinCreERT2_Arid3a fl/fl, 1month, replicate 1, scRNAseq
GSM7780017 VillinCreERT2_Arid3a fl/fl, 1month, replicate 2, scRNAseq
GSM7780018 VillinCreERT2, 1month, replicate 1, scRNAseq
Relations
BioProject PRJNA1016446

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Supplementary file Size Download File type/resource
GSE243155_RAW.tar 178.3 Mb (http)(custom) TAR (of TSV)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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