All-encomPASsing regulation of β-cells: PAS domain proteins in β-cell dysfunction and diabetes
Highlights • Many Per-Arnt-Sim (PAS) proteins are present in β-cells and some are dysregulated in diabetes. • The Hif1α pathway regulates β-cell differentiation possibly through altering metabolism. • Arnt regulates insulin secretion through heterodimerization with multiple bHLH-PAS factors. • Pask...
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Veröffentlicht in: | Trends in endocrinology and metabolism 2015-01, Vol.26 (1), p.49-57 |
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description | Highlights • Many Per-Arnt-Sim (PAS) proteins are present in β-cells and some are dysregulated in diabetes. • The Hif1α pathway regulates β-cell differentiation possibly through altering metabolism. • Arnt regulates insulin secretion through heterodimerization with multiple bHLH-PAS factors. • Pask may play important roles in regulating both α- and β-cell function. |
doi_str_mv | 10.1016/j.tem.2014.11.002 |
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Lynn, Francis C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-3ad5bb41a8ad37252fa6147f67d7421df7b108200ba9553c700691243f1007c93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Arnt</topic><topic>Aryl Hydrocarbon Receptor Nuclear Translocator - chemistry</topic><topic>Aryl Hydrocarbon Receptor Nuclear Translocator - physiology</topic><topic>Basic Helix-Loop-Helix Transcription Factors - chemistry</topic><topic>Basic Helix-Loop-Helix Transcription Factors - physiology</topic><topic>Bmal1</topic><topic>circadian</topic><topic>Clock</topic><topic>diabetes</topic><topic>Diabetes Mellitus - genetics</topic><topic>Diabetes Mellitus - metabolism</topic><topic>Diabetes Mellitus - physiopathology</topic><topic>Drosophila Proteins - chemistry</topic><topic>Drosophila Proteins - physiology</topic><topic>Endocrinology & Metabolism</topic><topic>Hif1α</topic><topic>Humans</topic><topic>hypoxia</topic><topic>Hypoxia-Inducible Factor 1, alpha Subunit - chemistry</topic><topic>Hypoxia-Inducible Factor 1, alpha Subunit - physiology</topic><topic>insulin secretion</topic><topic>Insulin-Secreting Cells - pathology</topic><topic>Insulin-Secreting Cells - physiology</topic><topic>Npas4</topic><topic>Nuclear Proteins - chemistry</topic><topic>Nuclear Proteins - physiology</topic><topic>PAS domain</topic><topic>Pask</topic><topic>Per</topic><topic>Period Circadian Proteins - chemistry</topic><topic>Period Circadian Proteins - physiology</topic><topic>Protein Structure, Tertiary</topic><topic>Protein-Serine-Threonine Kinases - chemistry</topic><topic>Protein-Serine-Threonine Kinases - physiology</topic><topic>Sim</topic><topic>Transcription Factors - chemistry</topic><topic>Transcription Factors - physiology</topic><topic>Vhl</topic><topic>Von Hippel-Lindau Tumor Suppressor Protein - chemistry</topic><topic>Von Hippel-Lindau Tumor Suppressor Protein - physiology</topic><topic>β-cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sabatini, Paul V</creatorcontrib><creatorcontrib>Lynn, Francis C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Trends in endocrinology and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sabatini, Paul V</au><au>Lynn, Francis C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>All-encomPASsing regulation of β-cells: PAS domain proteins in β-cell dysfunction and diabetes</atitle><jtitle>Trends in endocrinology and metabolism</jtitle><addtitle>Trends Endocrinol Metab</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>26</volume><issue>1</issue><spage>49</spage><epage>57</epage><pages>49-57</pages><issn>1043-2760</issn><eissn>1879-3061</eissn><abstract>Highlights • Many Per-Arnt-Sim (PAS) proteins are present in β-cells and some are dysregulated in diabetes. • The Hif1α pathway regulates β-cell differentiation possibly through altering metabolism. • Arnt regulates insulin secretion through heterodimerization with multiple bHLH-PAS factors. • Pask may play important roles in regulating both α- and β-cell function.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><pmid>25500169</pmid><doi>10.1016/j.tem.2014.11.002</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Arnt Aryl Hydrocarbon Receptor Nuclear Translocator - chemistry Aryl Hydrocarbon Receptor Nuclear Translocator - physiology Basic Helix-Loop-Helix Transcription Factors - chemistry Basic Helix-Loop-Helix Transcription Factors - physiology Bmal1 circadian Clock diabetes Diabetes Mellitus - genetics Diabetes Mellitus - metabolism Diabetes Mellitus - physiopathology Drosophila Proteins - chemistry Drosophila Proteins - physiology Endocrinology & Metabolism Hif1α Humans hypoxia Hypoxia-Inducible Factor 1, alpha Subunit - chemistry Hypoxia-Inducible Factor 1, alpha Subunit - physiology insulin secretion Insulin-Secreting Cells - pathology Insulin-Secreting Cells - physiology Npas4 Nuclear Proteins - chemistry Nuclear Proteins - physiology PAS domain Pask Per Period Circadian Proteins - chemistry Period Circadian Proteins - physiology Protein Structure, Tertiary Protein-Serine-Threonine Kinases - chemistry Protein-Serine-Threonine Kinases - physiology Sim Transcription Factors - chemistry Transcription Factors - physiology Vhl Von Hippel-Lindau Tumor Suppressor Protein - chemistry Von Hippel-Lindau Tumor Suppressor Protein - physiology β-cells |
title | All-encomPASsing regulation of β-cells: PAS domain proteins in β-cell dysfunction and diabetes |
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