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Research resource: the pdx1 cistrome of pancreatic islets. | LitMetric

AI Article Synopsis

  • Pdx1 is a crucial transcription factor for pancreas development and function; its absence leads to pancreatic disorders in both mice and humans.
  • Heterozygous mutations in Pdx1 have been linked to different forms of diabetes in humans, highlighting its importance in metabolic health.
  • Recent research using chromatin immunoprecipitation sequencing has revealed that Pdx1 regulates a set of evolutionarily conserved target genes involved in the endocrine system, signaling pathways, and cell survival, helping to explain the consequences of Pdx1 deficiency.

Article Abstract

The homeodomain transcription factor pancreas duodenal homeobox 1 (Pdx1, also known as insulin promoter factor 1) is a master regulator of pancreas development, as mice or humans lacking Pdx1 function are a pancreatic. Importantly, heterozygous mutations in Pdx1 cause early and late onset forms of diabetes in humans. Despite these central roles in development and adult β-cell function, we have only rudimentary knowledge of the transcriptome targets of Pdx1 that mediate these phenotypes. Therefore, we performed global location analysis of Pdx1 occupancy in pancreatic islets. We used evolutionary conservation of target genes to identify the most relevant Pdx1 targets by performing chromatin immunoprecipitation sequencing on both human and mouse islets. Remarkably, the conserved target set is highly enriched for genes annotated to function in endocrine system and metabolic disorders, various signaling pathways, and cell survival, providing a molecular explanation for many of the phenotypes resulting from Pdx1 deficiency.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3286194PMC
http://dx.doi.org/10.1210/me.2011-1231DOI Listing

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