The Krüppel-like zinc finger protein Glis3 directly and indirectly activates insulin gene transcription

Yisheng Yang, Benny Hung Junn Chang, Susan L. Samson, Ming V. Li, Lawrence Chan

Research output: Contribution to journalArticlepeer-review

56 Scopus citations

Abstract

Glis3 is a member of the Krüppel-like family of transcription factors and is highly expressed in islet β cells. Mutations in GLIS3 cause the syndrome of neonatal diabetes and congenital hypothyroidism (NDH). Our aim was to examine the role of Glis3 in β cells, specifically with regard to regulation of insulin gene transcription. We demonstrate that insulin 2 (Ins2) mRNA expression in rat insulinoma 832/13 cells is markedly increased by wild-type Glis3 overexpression, but not by the NDH1 mutant. Furthermore, expression of both Ins1 and Ins2 mRNA is downregulated when Glis3 is knocked down by siRNA. Glis3 binds to the Ins2 promoter in the cell, detected by chromatin immunoprecipitation. Deletion analysis of Ins2 promoter identifies a sequence (5′-GTCCCCTGCTGTGAA-3′) from -255 to -241 as the Glis3 response element and binding occur specifically via the Glis3 zinc finger region as revealed by mobility shift assays. Moreover, Glis3 physically and functionally interacts with Pdx1, MafA and NeuroD1 to modulate Ins2 promoter activity. Glis3 also may indirectly affect insulin promoter activity through upregulation of MafA and downregulation of Nkx6-1. This study uncovers a role of Glis3 for regulation of insulin gene expression and expands our understanding of its role in the β cell.

Original languageEnglish (US)
Pages (from-to)2529-2538
Number of pages10
JournalNucleic acids research
Volume37
Issue number8
DOIs
StatePublished - 2009

Bibliographical note

Funding Information:
US National Institutes of Health (NIH) grant DK-68037 (to L.C.); the Diabetes and Endocrinology Research Center (P30DK079638); the Rutherford Chair from St Luke’s Episcopal Hospital; T.T. & W.F. Chao Foundation. Funding for open access charge: National Institutes of Health.

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