Cdx2 transcription factor binding in intestinal villus and gene expression profiling in Cdx mutant mice
Source: NCBI BioProject (ID PRJNA132465)
Source: NCBI BioProject (ID PRJNA132465)
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Project name: Mus musculus
Description: We conditionally inactivated mouse Cdx2, a dominant regulator of intestinal development, and mapped its genome occupancy in adult intestinal villi. Although homeotic transformation, observed in Cdx2-null embryos, was absent in mutant adults, gene expression and cell morphology were vitally compromised. Lethality was accelerated in mice lacking both Cdx2 and its homolog Cdx1, with exaggeration of defects in crypt cell replication and enterocyte differentiation. Cdx2 occupancy correlated with hundreds of transcripts that fell but not with equal numbers that rose with Cdx loss, indicating a predominantly activating role at intestinal cis-regulatory regions. Integrated consideration of a mutant phenotype and cistrome hence reveals the continued and distinct requirement in adults of a master developmental regulator that activates tissue-specific genes.Overall design: Cdx2 ChIP-seq in mouse villus, and gene expression data from Cdx1, Cdx2 and compound knockout mouse intestine
Data type: Other
Sample scope: Multiisolate
Relevance: ModelOrganism
Organization: Verzi, Genetics, Rutgers, the State University of New Jersey
Literatures
- PMID: 21402776
Release date: 2011-04-13
Last updated: 2010-10-12