Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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The transcriptional repressor Blimp1/Prdm1 regulates post-natal reprogramming of intestinal enterocytes

ABSTRACT: Expression profiling of Prdm1 mutant E18.5 small intestine was performed using Illumina whole genome V2 arrays. The hypothesis tested in the present study was that Blimp1 regulates the transcription of key genes involved in enterocyte differentiation and survival. Results identify substantial and premature activation of key components of the adult enterocyte biochemical signature. Villin-Cre and Prdm1BEH/+ animals were intercrossed to generate heterozygous Villin-Cre, Prdm1BEH males that were then mated with homozygous Prdm1 CA/CA females carrying the R26R allele to generate Prdm1+/+ (Prdm1CA/+) or Prdm1-/- (Villin-Cre, Prdm1CA/BEH) offspring. Total RNA obtained from 11 Prdm1+/+ and 10 Prdm1-/- E18.5 small intestine samples was hybridized to Illumina WG6_V2 beadchips.

ORGANISM(S): Mus musculus

SUBMITTER: Arne Mould 

PROVIDER: E-GEOD-29658 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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The transcriptional repressor Blimp1/Prdm1 regulates postnatal reprogramming of intestinal enterocytes.

Harper James J   Mould Arne A   Andrews Robert M RM   Bikoff Elizabeth K EK   Robertson Elizabeth J EJ  

Proceedings of the National Academy of Sciences of the United States of America 20110613 26

Female mammals produce milk to feed their newborn offspring before teeth develop and permit the consumption of solid food. Intestinal enterocytes dramatically alter their biochemical signature during the suckling-to-weaning transition. The transcriptional repressor Blimp1 is strongly expressed in immature enterocytes in utero, but these are gradually replaced by Blimp1(-) crypt-derived adult enterocytes. Here we used a conditional inactivation strategy to eliminate Blimp1 function in the develop  ...[more]

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