| Literature DB >> 33658226 |
Alexandra Theis1, Ruth A Singer2,3, Diana Garofalo2, Alexander Paul2,4, Anila Narayana1, Lori Sussel5,2.
Abstract
Groucho-related genes (GRGs) are transcriptional co-repressors that are crucial for many developmental processes. Several essential pancreatic transcription factors are capable of interacting with GRGs; however, the in vivo role of GRG-mediated transcriptional repression in pancreas development is still not well understood. In this study, we used complex mouse genetics and transcriptomic analyses to determine that GRG3 is essential for β cell development, and in the absence of Grg3 there is compensatory upregulation of Grg4 Grg3/4 double mutant mice have severe dysregulation of the pancreas gene program with ectopic expression of canonical liver genes and Foxa1, a master regulator of the liver program. Neurod1, an essential β cell transcription factor and predicted target of Foxa1, becomes downregulated in Grg3/4 mutants, resulting in reduced β cell proliferation, hyperglycemia, and early lethality. These findings uncover novel functions of GRG-mediated repression during pancreas development.Entities:
Keywords: Foxa1; Groucho/TLE co-repressor; Mouse; Pancreas development; β cells
Mesh:
Substances:
Year: 2021 PMID: 33658226 PMCID: PMC8015241 DOI: 10.1242/dev.192401
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.868