Groucho co-repressor proteins regulate β cell development and proliferation by repressing Foxa1 in the developing mouse pancreas.
Alexandra TheisRuth A SingerDiana GarofaloAlexander PaulAnila NarayanaLori SusselPublished in: Development (Cambridge, England) (2021)
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.
Keyphrases
- transcription factor
- single cell
- cell proliferation
- genome wide identification
- cell therapy
- poor prognosis
- gene expression
- dna binding
- signaling pathway
- genome wide
- quality improvement
- rna seq
- type diabetes
- cell cycle
- skeletal muscle
- stem cells
- metabolic syndrome
- adipose tissue
- bone marrow
- oxidative stress
- protein kinase
- copy number
- heat stress