Dataset Information

Integrative multi-omics analysis of intestinal organoid differentiation

ABSTRACT: Intestinal organoids accurately recapitulate epithelial homeostasis in vivo, thereby representing a powerful in vitro system to investigate lineage specification and cellular differentiation. Here, we applied a multi-omics framework on stem cell enriched and -depleted mouse intestinal organoids to obtain a holistic view of the molecular mechanisms that drive differential gene expression during adult intestinal stem cell differentiation. Our data revealed a global rewiring of the transcriptome and proteome between intestinal stem cells and enterocytes, with the majority of dynamic protein expression being transcription-driven. Integrating absolute mRNA and protein copy numbers revealed post-transcriptional regulation of gene expression. Probing the epigenetic landscape identified a large number of cell-type specific regulatory elements, which revealed Hnf4g as a major driver of enterocyte differentiation. In summary, by applying an integrative systems biology approach we uncovered multiple layers of gene expression regulation, which contribute to lineage specification and plasticity of the mouse small intestinal epithelium.

OTHER RELATED OMICS DATASETS IN: GSE114113

INSTRUMENT(S): LTQ Orbitrap XL, Orbitrap Fusion, Q Exactive

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Intestinal Epithelium, Small Intestine

SUBMITTER: Rik Lindeboom

LAB HEAD: Michiel Vermeulen

PROVIDER: PXD009700 | Pride | 2018-06-25

REPOSITORIES: Pride

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Dataset's files

Source:

			Action	DRS
	20141031_Fusion1_SA_PJ_HS_smallint_mouse_crypt_sax_tr1_FT.raw	Raw
	20141031_Fusion1_SA_PJ_HS_smallint_mouse_crypt_sax_tr1_ibaq.raw	Raw
	20141031_Fusion1_SA_PJ_HS_smallint_mouse_crypt_sax_tr1_pH11.raw	Raw
	20141031_Fusion1_SA_PJ_HS_smallint_mouse_crypt_sax_tr1_pH2.raw	Raw
	20141031_Fusion1_SA_PJ_HS_smallint_mouse_crypt_sax_tr1_pH5.raw	Raw

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Publications

Integrative multi-omics analysis of intestinal organoid differentiation.

Lindeboom Rik Gh RG van Voorthuijsen Lisa L Oost Koen C KC Rodríguez-Colman Maria J MJ Luna-Velez Maria V MV Furlan Cristina C Baraille Floriane F Jansen Pascal Wtc PW Ribeiro Agnès A Burgering Boudewijn Mt BM Snippert Hugo J HJ Vermeulen Michiel M

Molecular systems biology 20180626 6

Intestinal organoids accurately recapitulate epithelial homeostasis <i>in vivo</i>, thereby representing a powerful <i>in vitro</i> system to investigate lineage specification and cellular differentiation. Here, we applied a multi-omics framework on stem cell-enriched and stem cell-depleted mouse intestinal organoids to obtain a holistic view of the molecular mechanisms that drive differential gene expression during adult intestinal stem cell differentiation. Our data revealed a global rewiring ...[more]

PMID: 29945941

Similar Datasets

Project description:The endodermal lining of the adult gastro-intestinal tract harbors stem cells that are responsible for the day-to-day regeneration of the epithelium. Stem cells residing in the pyloric glands of the stomach and in the small intestinal crypts differ in their differentiation program and in the gene repertoire that they express. Both types of stem cells have been shown to grow from single cells into 3D structures (organoids) in vitro. We show that single adult Lgr5-positive stem cells, isolated from small intestinal organoids, require Cdx2 to maintain their intestinal identity and are converted cell-autonomously into pyloric stem cells in the absence of this transcription factor. Clonal descendants of Cdx2null small intestinal stem cells enter the gastric differentiation program instead of producing intestinal derivatives. Conversely, forced expression of Cdx2 in gastric organoids results in their intestinalization. The intestinal genetic program is thus critically dependent on the single transcription factor encoding gene Cdx2. Small intestinal crypts and stomach glands were isolated from Cdx2-/fl / Lgr5-EGFP-CreERT2 mice and cultured for a week in order to generate small intestinal (SI) and stomach (Sto) in vitro organoids. The Lgr5-CreERT2 enzyme activity has been induced by overnight 4-hydroxytamoxifen induction. Tamoxifen treated and untreated Lgr5-EGFPhi SI and Sto stem cells were FACS sorted and seeded back into ENRWfg (Sto med) culture conditions in order to generate Cdx2-/fl small intestinal (Control SI), Cdx2null small intestinal (Cdx2null SI) and Cdx2-/fl stomach (Control Sto) clonal organoids. Cdx2-/fl SI organoids and Cdx2-/fl Sto organoids have been also cultured in ENR (SI med) to induce differentiation. After some passages of clonal organoid expansion, RNA was isolated from Control SI, Cdx2null SI and Control Sto Lgr5-EGFPhi FACS sorted stem cell populations and from smal intestinal and stomach organoids cultured in different conditions and hybridized on Affymetrix Mouse Gene ST 1.1 arrays.