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Comparative gene expression profiling in small intestinal mucosa of Rbm47 intestine-specific knock-out and wt mice

ABSTRACT: Comparative gene expression profiling in small intestinal mucosa of Rbm47 intestine-specific knock-out and wt mice

PROVIDER: PRJNA851031 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR19753461.fastq.gz	Fastqsanger.gz
	SRR19753462.fastq.gz	Fastqsanger.gz
	SRR19753463.fastq.gz	Fastqsanger.gz
	SRR19753464.fastq.gz	Fastqsanger.gz
	SRR19753465.fastq.gz	Fastqsanger.gz

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Comparative gene expression profiling in small intestinal mucosa of Rbm47 intestine-specific knock-out and wt mice

Project description:Rationale: RNA binding protein 47 (RBM47) is required for embryonic endoderm development but a role in adult intestine is unknown. Objective: We studied intestine-specific Rbm47 knockout mice (Rbm47-IKO) following intestinal injury and made crosses into Apcmin/+ mice to examine alterations in intestinal proliferation, response to injury and tumorigenesis. We also interrogated human colorectal polyps and colon carcinoma tissue. Findings: Rbm47-IKO mice exhibit increased proliferation, abnormal villus morphology and cellularity, with corresponding changes in Rbm47-IKO organoids. Rbm47-IKO mice adapt to radiation injury and are protected against chemical-induced colitis, with Rbm47-IKO intestine showing upregulation of antioxidant and Wnt signaling pathways as well as stem cell and developmental genes. Furthermore, Rbm47-IKO mice are protected against colitis-associated cancer. By contrast, aged Rbm47-IKO mice develop spontaneous polyposis and Rbm47-IKO, Apcmin/+ mice manifest an increased intestinal polyp burden. RBM47 mRNA was decreased in human colorectal cancer versus paired normal tissue along with alternative splicing of TJP1 mRNA. Public databases revealed stage-specific reduction in RBM47 expression in colorectal cancer, associated independently with decreased overall survival. Conclusions: These findings implicate RBM47 as a cell-intrinsic modifier of intestinal growth, inflammatory and tumorigenic pathways.

2023-05-31 | GSE206461 | GEO

Raw RNA-seq data of small intestine tissue from control and Lats1/2 knock out mice

Project description:Raw RNA-seq data of small intestine tissue from control and Lats1/2 knock out mice

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Project description:Comparision of gene expression profiles of intestine, kidney and liver tissues of adult male knock-out mice for all Cyp3a genes (Cyp3a-/- genotype) versus adult male wild-type control mice (FVB genotype).

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aerobic knock-out

Project description:Six different knock-out strains' expression data under aerobic condition Keywords: parallel sample

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Project description:Six different knock-out strains' expression data under anaerobic condition Keywords: parallel sample

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Expression data from Amacr knock-out mouse intestine

Project description:Bile acids play multiple roles in vertebrate metabolism by facilitating lipid absorption in the intestine and acting as a signaling molecule in lipid and carbohydrate metabolism. Bile acids are also the main route to excrete excess cholesterol out of the body. Alpha-methyl-Coa racemase (Amacr) is one of the enzymes needed to produce bile acids from cholesterol. The mouse model lacking Amacr can produce only minor (less than 10%) amounts of bile acids, but still they are symptomless in normal laboratory conditions. Cholesterol absorption occurs in the jejunum part of the intestine. In this experiment, the intestines from Amacr-/- and wild-type mice were divided into four equal segments and the endothelial layer was collected by scraping. The RNA from these samples was isolated and the gene expression levels in each segment were compared. 3 biological replicates per genotype/segment combination.

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Raw RNA-seq data of small intestine tissue from control and Lats1/2 knock out mice

Project description:Raw RNA-seq data of small intestine tissue from control and Lats1/2 knock out mice

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