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The role of ADP-ribose metabolism in metabolic regulation, adipose tissue differentiation, and metabolism
Poly(ADP-ribose) polymerases (PARPs or ARTDs), originally described as DNA repair factors, have metabolic regulatory roles. PARP1, PARP2, PARP7, PARP10, and PARP14 regulate central and peripheral carbohydrate and lipid metabolism and often channel pathological disruptive metabolic signals. PARP1 and...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Cold Spring Harbor Laboratory Press
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7050491/ https://www.ncbi.nlm.nih.gov/pubmed/32029456 http://dx.doi.org/10.1101/gad.334284.119 |
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author | Szántó, Magdolna Bai, Peter |
author_facet | Szántó, Magdolna Bai, Peter |
author_sort | Szántó, Magdolna |
collection | PubMed |
description | Poly(ADP-ribose) polymerases (PARPs or ARTDs), originally described as DNA repair factors, have metabolic regulatory roles. PARP1, PARP2, PARP7, PARP10, and PARP14 regulate central and peripheral carbohydrate and lipid metabolism and often channel pathological disruptive metabolic signals. PARP1 and PARP2 are crucial for adipocyte differentiation, including the commitment toward white, brown, or beige adipose tissue lineages, as well as the regulation of lipid accumulation. Through regulating adipocyte function and organismal energy balance, PARPs play a role in obesity and the consequences of obesity. These findings can be translated into humans, as evidenced by studies on identical twins and SNPs affecting PARP activity. |
format | Online Article Text |
id | pubmed-7050491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-70504912020-03-16 The role of ADP-ribose metabolism in metabolic regulation, adipose tissue differentiation, and metabolism Szántó, Magdolna Bai, Peter Genes Dev Special Section: Review Poly(ADP-ribose) polymerases (PARPs or ARTDs), originally described as DNA repair factors, have metabolic regulatory roles. PARP1, PARP2, PARP7, PARP10, and PARP14 regulate central and peripheral carbohydrate and lipid metabolism and often channel pathological disruptive metabolic signals. PARP1 and PARP2 are crucial for adipocyte differentiation, including the commitment toward white, brown, or beige adipose tissue lineages, as well as the regulation of lipid accumulation. Through regulating adipocyte function and organismal energy balance, PARPs play a role in obesity and the consequences of obesity. These findings can be translated into humans, as evidenced by studies on identical twins and SNPs affecting PARP activity. Cold Spring Harbor Laboratory Press 2020-03-01 /pmc/articles/PMC7050491/ /pubmed/32029456 http://dx.doi.org/10.1101/gad.334284.119 Text en © 2020 Szántó and Bai; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by/4.0/ This article, published in Genes & Development, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Special Section: Review Szántó, Magdolna Bai, Peter The role of ADP-ribose metabolism in metabolic regulation, adipose tissue differentiation, and metabolism |
title | The role of ADP-ribose metabolism in metabolic regulation, adipose tissue differentiation, and metabolism |
title_full | The role of ADP-ribose metabolism in metabolic regulation, adipose tissue differentiation, and metabolism |
title_fullStr | The role of ADP-ribose metabolism in metabolic regulation, adipose tissue differentiation, and metabolism |
title_full_unstemmed | The role of ADP-ribose metabolism in metabolic regulation, adipose tissue differentiation, and metabolism |
title_short | The role of ADP-ribose metabolism in metabolic regulation, adipose tissue differentiation, and metabolism |
title_sort | role of adp-ribose metabolism in metabolic regulation, adipose tissue differentiation, and metabolism |
topic | Special Section: Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7050491/ https://www.ncbi.nlm.nih.gov/pubmed/32029456 http://dx.doi.org/10.1101/gad.334284.119 |
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