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Avian and Mammalian Facilitative Glucose Transporters

The GLUT members belong to a family of glucose transporter proteins that facilitate glucose transport across the cell membrane. The mammalian GLUT family consists of thirteen members (GLUTs 1–12 and H(+)-myo-inositol transporter (HMIT)). Humans have a recently duplicated GLUT member, GLUT14. Avians...

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Detalles Bibliográficos
Autores principales: Byers, Mary Shannon, Howard, Christianna, Wang, Xiaofei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487954/
https://www.ncbi.nlm.nih.gov/pubmed/28379195
http://dx.doi.org/10.3390/microarrays6020007
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author Byers, Mary Shannon
Howard, Christianna
Wang, Xiaofei
author_facet Byers, Mary Shannon
Howard, Christianna
Wang, Xiaofei
author_sort Byers, Mary Shannon
collection PubMed
description The GLUT members belong to a family of glucose transporter proteins that facilitate glucose transport across the cell membrane. The mammalian GLUT family consists of thirteen members (GLUTs 1–12 and H(+)-myo-inositol transporter (HMIT)). Humans have a recently duplicated GLUT member, GLUT14. Avians express the majority of GLUT members. The arrangement of multiple GLUTs across all somatic tissues signifies the important role of glucose across all organisms. Defects in glucose transport have been linked to metabolic disorders, insulin resistance and diabetes. Despite the essential importance of these transporters, our knowledge regarding GLUT members in avians is fragmented. It is clear that there are no chicken orthologs of mammalian GLUT4 and GLUT7. Our examination of GLUT members in the chicken revealed that some chicken GLUT members do not have corresponding orthologs in mammals. We review the information regarding GLUT orthologs and their function and expression in mammals and birds, with emphasis on chickens and humans.
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spelling pubmed-54879542017-06-30 Avian and Mammalian Facilitative Glucose Transporters Byers, Mary Shannon Howard, Christianna Wang, Xiaofei Microarrays (Basel) Review The GLUT members belong to a family of glucose transporter proteins that facilitate glucose transport across the cell membrane. The mammalian GLUT family consists of thirteen members (GLUTs 1–12 and H(+)-myo-inositol transporter (HMIT)). Humans have a recently duplicated GLUT member, GLUT14. Avians express the majority of GLUT members. The arrangement of multiple GLUTs across all somatic tissues signifies the important role of glucose across all organisms. Defects in glucose transport have been linked to metabolic disorders, insulin resistance and diabetes. Despite the essential importance of these transporters, our knowledge regarding GLUT members in avians is fragmented. It is clear that there are no chicken orthologs of mammalian GLUT4 and GLUT7. Our examination of GLUT members in the chicken revealed that some chicken GLUT members do not have corresponding orthologs in mammals. We review the information regarding GLUT orthologs and their function and expression in mammals and birds, with emphasis on chickens and humans. MDPI 2017-04-05 /pmc/articles/PMC5487954/ /pubmed/28379195 http://dx.doi.org/10.3390/microarrays6020007 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Byers, Mary Shannon
Howard, Christianna
Wang, Xiaofei
Avian and Mammalian Facilitative Glucose Transporters
title Avian and Mammalian Facilitative Glucose Transporters
title_full Avian and Mammalian Facilitative Glucose Transporters
title_fullStr Avian and Mammalian Facilitative Glucose Transporters
title_full_unstemmed Avian and Mammalian Facilitative Glucose Transporters
title_short Avian and Mammalian Facilitative Glucose Transporters
title_sort avian and mammalian facilitative glucose transporters
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487954/
https://www.ncbi.nlm.nih.gov/pubmed/28379195
http://dx.doi.org/10.3390/microarrays6020007
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