GLIS3: A Critical Transcription Factor in Islet β-Cell Generation

Understanding of pancreatic islet biology has greatly increased over the past few decades based in part on an increased understanding of the transcription factors that guide this process. One such transcription factor that has been increasingly tied to both β-cell development and the development of...

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Main Authors: David W. Scoville, Anton M. Jetten
Format: Article
Language:English
Published: MDPI AG 2021-12-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/10/12/3471
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author David W. Scoville
Anton M. Jetten
author_facet David W. Scoville
Anton M. Jetten
author_sort David W. Scoville
collection DOAJ
description Understanding of pancreatic islet biology has greatly increased over the past few decades based in part on an increased understanding of the transcription factors that guide this process. One such transcription factor that has been increasingly tied to both β-cell development and the development of diabetes in humans is <i>GLIS3</i>. Genetic deletion of <i>GLIS3</i> in mice and humans induces neonatal diabetes, while single nucleotide polymorphisms (SNPs) in <i>GLIS3</i> have been associated with both Type 1 and Type 2 diabetes. As a significant progress has been made in understanding some of <i>GLIS3</i>’s roles in pancreas development and diabetes, we sought to compare current knowledge on <i>GLIS3</i> within the pancreas to that of other islet enriched transcription factors. While <i>GLIS3</i> appears to regulate similar genes and pathways to other transcription factors, its unique roles in β-cell development and maturation make it a key target for future studies and therapy.
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spelling doaj.art-4456222782dc477d970250d0c9fdb6762023-11-23T07:38:14ZengMDPI AGCells2073-44092021-12-011012347110.3390/cells10123471GLIS3: A Critical Transcription Factor in Islet β-Cell GenerationDavid W. Scoville0Anton M. Jetten1Cell Biology Group, Immunity, Inflammation and Disease Laboratory, National Institute of Environmental Health Science, National Institutes of Health, Durham, NC 27709, USACell Biology Group, Immunity, Inflammation and Disease Laboratory, National Institute of Environmental Health Science, National Institutes of Health, Durham, NC 27709, USAUnderstanding of pancreatic islet biology has greatly increased over the past few decades based in part on an increased understanding of the transcription factors that guide this process. One such transcription factor that has been increasingly tied to both β-cell development and the development of diabetes in humans is <i>GLIS3</i>. Genetic deletion of <i>GLIS3</i> in mice and humans induces neonatal diabetes, while single nucleotide polymorphisms (SNPs) in <i>GLIS3</i> have been associated with both Type 1 and Type 2 diabetes. As a significant progress has been made in understanding some of <i>GLIS3</i>’s roles in pancreas development and diabetes, we sought to compare current knowledge on <i>GLIS3</i> within the pancreas to that of other islet enriched transcription factors. While <i>GLIS3</i> appears to regulate similar genes and pathways to other transcription factors, its unique roles in β-cell development and maturation make it a key target for future studies and therapy.https://www.mdpi.com/2073-4409/10/12/3471GLIS3pancreasdiabetesdevelopment
spellingShingle David W. Scoville
Anton M. Jetten
GLIS3: A Critical Transcription Factor in Islet β-Cell Generation
Cells
GLIS3
pancreas
diabetes
development
title GLIS3: A Critical Transcription Factor in Islet β-Cell Generation
title_full GLIS3: A Critical Transcription Factor in Islet β-Cell Generation
title_fullStr GLIS3: A Critical Transcription Factor in Islet β-Cell Generation
title_full_unstemmed GLIS3: A Critical Transcription Factor in Islet β-Cell Generation
title_short GLIS3: A Critical Transcription Factor in Islet β-Cell Generation
title_sort glis3 a critical transcription factor in islet β cell generation
topic GLIS3
pancreas
diabetes
development
url https://www.mdpi.com/2073-4409/10/12/3471
work_keys_str_mv AT davidwscoville glis3acriticaltranscriptionfactorinisletbcellgeneration
AT antonmjetten glis3acriticaltranscriptionfactorinisletbcellgeneration