1. Academic Validation
  2. The transcription factor Rfx3 regulates beta-cell differentiation, function, and glucokinase expression

The transcription factor Rfx3 regulates beta-cell differentiation, function, and glucokinase expression

  • Diabetes. 2010 Jul;59(7):1674-85. doi: 10.2337/db09-0986.
Aouatef Ait-Lounis 1 Claire Bonal Queralt Seguín-Estévez Christoph D Schmid Philipp Bucher Pedro L Herrera Bénédicte Durand Paolo Meda Walter Reith
Affiliations

Affiliation

  • 1 Department of Pathology and Immunology, Faculty of Medicine, University of Geneva, Centre Médical Universitaire, Geneva, Switzerland.
Abstract

Objective: Pancreatic islets of perinatal mice lacking the transcription factor Rfx3 exhibit a marked reduction in insulin-producing beta-cells. The objective of this work was to unravel the cellular and molecular mechanisms underlying this deficiency.

Research design and methods: Immunofluorescence studies and quantitative RT-PCR experiments were used to study the emergence of insulin-positive cells, the expression of transcription factors implicated in the differentiation of beta-cells from endocrine progenitors, and the expression of mature beta-cell markers during development in Rfx3(-/-) and pancreas-specific Rfx3-knockout mice. RNA interference experiments were performed to document the consequences of downregulating Rfx3 expression in Min6 beta-cells. Quantitative chromatin immunoprecipitation (ChIP), ChIP Sequencing, and bandshift experiments were used to identify Rfx3 target genes.

Results: Reduced development of insulin-positive cells in Rfx3(-/-) mice was not due to deficiencies in endocrine progenitors or beta-lineage specification, but reflected the accumulation of insulin-positive beta-cell precursors and defective beta-cells exhibiting reduced Insulin, Glut-2, and Gck expression. Similar incompletely differentiated beta-cells developed in pancreas-specific Rfx3-deficient embryos. Defective beta-cells lacking Glut-2 and Gck expression dominate in Rfx3-deficent adults, leading to glucose intolerance. Attenuated Glut-2 and Glucokinase expression, and impaired glucose-stimulated Insulin secretion, were also induced by RNA interference-mediated inhibition of Rfx3 expression in Min6 cells. Finally, Rfx3 was found to bind in Min6 cells and human islets to two well-known regulatory sequences, Pal-1 and Pal-2, in the neuroendocrine promoter of the Glucokinase gene.

Conclusions: Our results show that Rfx3 is required for the differentiation and function of mature beta-cells and regulates the beta-cell promoter of the Glucokinase gene.

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