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Prep1, A Homeodomain Transcription Factor Involved in Glucose and Lipid Metabolism
The three-amino acid loop extension (TALE) homeodomain proteins are a family of transcription factor including the mammalian Pbx, MEIS and Prep proteins. TALE proteins can bind other transcription factors such as Pdx-1 and play an important role in the regulation of glucose metabolism. Experiments p...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032887/ https://www.ncbi.nlm.nih.gov/pubmed/30002646 http://dx.doi.org/10.3389/fendo.2018.00346 |
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author | Oriente, Francesco Perruolo, Giuseppe Cimmino, Ilaria Cabaro, Serena Liotti, Antonietta Longo, Michele Miele, Claudia Formisano, Pietro Beguinot, Francesco |
author_facet | Oriente, Francesco Perruolo, Giuseppe Cimmino, Ilaria Cabaro, Serena Liotti, Antonietta Longo, Michele Miele, Claudia Formisano, Pietro Beguinot, Francesco |
author_sort | Oriente, Francesco |
collection | PubMed |
description | The three-amino acid loop extension (TALE) homeodomain proteins are a family of transcription factor including the mammalian Pbx, MEIS and Prep proteins. TALE proteins can bind other transcription factors such as Pdx-1 and play an important role in the regulation of glucose metabolism. Experiments performed in mutant mice have shown that while the single Pbx1 or Pdx-1 knockout mice feature pancreatic islet malformations, impaired glucose tolerance and hypoinsulinemia, the trans-heterozygous Pbx1(+/−) Pdx1(+/−) mice develop age-dependent overt diabetes mellitus. In contrast, Prep1 plays a different role with respect to these proteins. Indeed, Prep1 hypomorphic mice, expressing low levels of protein, feature pancreatic islet hypoplasia accompanied by hypoinsulinemia similar to Pbx1 or Pdx1. Nevertheless, these animals show increased insulin sensitivity in skeletal muscle, liver and adipose tissue accompanied by protection from streptozotocin-induced diabetes. In addition, Prep1 hypomorphic mice feature reduced triglyceride synthesis and do not develop steatohepatitis after a methionine and coline deficient diet. In this review we have underlined how important metabolic functions are controlled by TALE proteins, in particular by Prep1, leading to hypothesis that its suppression might represent beneficial effect in the care of metabolic diseases. |
format | Online Article Text |
id | pubmed-6032887 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60328872018-07-12 Prep1, A Homeodomain Transcription Factor Involved in Glucose and Lipid Metabolism Oriente, Francesco Perruolo, Giuseppe Cimmino, Ilaria Cabaro, Serena Liotti, Antonietta Longo, Michele Miele, Claudia Formisano, Pietro Beguinot, Francesco Front Endocrinol (Lausanne) Endocrinology The three-amino acid loop extension (TALE) homeodomain proteins are a family of transcription factor including the mammalian Pbx, MEIS and Prep proteins. TALE proteins can bind other transcription factors such as Pdx-1 and play an important role in the regulation of glucose metabolism. Experiments performed in mutant mice have shown that while the single Pbx1 or Pdx-1 knockout mice feature pancreatic islet malformations, impaired glucose tolerance and hypoinsulinemia, the trans-heterozygous Pbx1(+/−) Pdx1(+/−) mice develop age-dependent overt diabetes mellitus. In contrast, Prep1 plays a different role with respect to these proteins. Indeed, Prep1 hypomorphic mice, expressing low levels of protein, feature pancreatic islet hypoplasia accompanied by hypoinsulinemia similar to Pbx1 or Pdx1. Nevertheless, these animals show increased insulin sensitivity in skeletal muscle, liver and adipose tissue accompanied by protection from streptozotocin-induced diabetes. In addition, Prep1 hypomorphic mice feature reduced triglyceride synthesis and do not develop steatohepatitis after a methionine and coline deficient diet. In this review we have underlined how important metabolic functions are controlled by TALE proteins, in particular by Prep1, leading to hypothesis that its suppression might represent beneficial effect in the care of metabolic diseases. Frontiers Media S.A. 2018-06-28 /pmc/articles/PMC6032887/ /pubmed/30002646 http://dx.doi.org/10.3389/fendo.2018.00346 Text en Copyright © 2018 Oriente, Perruolo, Cimmino, Cabaro, Liotti, Longo, Miele, Formisano and Beguinot. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Oriente, Francesco Perruolo, Giuseppe Cimmino, Ilaria Cabaro, Serena Liotti, Antonietta Longo, Michele Miele, Claudia Formisano, Pietro Beguinot, Francesco Prep1, A Homeodomain Transcription Factor Involved in Glucose and Lipid Metabolism |
title | Prep1, A Homeodomain Transcription Factor Involved in Glucose and Lipid Metabolism |
title_full | Prep1, A Homeodomain Transcription Factor Involved in Glucose and Lipid Metabolism |
title_fullStr | Prep1, A Homeodomain Transcription Factor Involved in Glucose and Lipid Metabolism |
title_full_unstemmed | Prep1, A Homeodomain Transcription Factor Involved in Glucose and Lipid Metabolism |
title_short | Prep1, A Homeodomain Transcription Factor Involved in Glucose and Lipid Metabolism |
title_sort | prep1, a homeodomain transcription factor involved in glucose and lipid metabolism |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032887/ https://www.ncbi.nlm.nih.gov/pubmed/30002646 http://dx.doi.org/10.3389/fendo.2018.00346 |
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