Cargando…
Histone H4 lysine 16 acetylation controls central carbon metabolism and diet-induced obesity in mice
Noncommunicable diseases (NCDs) account for over 70% of deaths world-wide. Previous work has linked NCDs such as type 2 diabetes (T2D) to disruption of chromatin regulators. However, the exact molecular origins of these chronic conditions remain elusive. Here, we identify the H4 lysine 16 acetyltran...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551339/ https://www.ncbi.nlm.nih.gov/pubmed/34707105 http://dx.doi.org/10.1038/s41467-021-26277-w |
_version_ | 1784591134967726080 |
---|---|
author | Pessoa Rodrigues, Cecilia Chatterjee, Aindrila Wiese, Meike Stehle, Thomas Szymanski, Witold Shvedunova, Maria Akhtar, Asifa |
author_facet | Pessoa Rodrigues, Cecilia Chatterjee, Aindrila Wiese, Meike Stehle, Thomas Szymanski, Witold Shvedunova, Maria Akhtar, Asifa |
author_sort | Pessoa Rodrigues, Cecilia |
collection | PubMed |
description | Noncommunicable diseases (NCDs) account for over 70% of deaths world-wide. Previous work has linked NCDs such as type 2 diabetes (T2D) to disruption of chromatin regulators. However, the exact molecular origins of these chronic conditions remain elusive. Here, we identify the H4 lysine 16 acetyltransferase MOF as a critical regulator of central carbon metabolism. High-throughput metabolomics unveil a systemic amino acid and carbohydrate imbalance in Mof deficient mice, manifesting in T2D predisposition. Oral glucose tolerance testing (OGTT) reveals defects in glucose assimilation and insulin secretion in these animals. Furthermore, Mof deficient mice are resistant to diet-induced fat gain due to defects in glucose uptake in adipose tissue. MOF-mediated H4K16ac deposition controls expression of the master regulator of glucose metabolism, Pparg and the entire downstream transcriptional network. Glucose uptake and lipid storage can be reconstituted in MOF-depleted adipocytes in vitro by ectopic Glut4 expression, PPARγ agonist thiazolidinedione (TZD) treatment or SIRT1 inhibition. Hence, chronic imbalance in H4K16ac promotes a destabilisation of metabolism triggering the development of a metabolic disorder, and its maintenance provides an unprecedented regulatory epigenetic mechanism controlling diet-induced obesity. |
format | Online Article Text |
id | pubmed-8551339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85513392021-10-29 Histone H4 lysine 16 acetylation controls central carbon metabolism and diet-induced obesity in mice Pessoa Rodrigues, Cecilia Chatterjee, Aindrila Wiese, Meike Stehle, Thomas Szymanski, Witold Shvedunova, Maria Akhtar, Asifa Nat Commun Article Noncommunicable diseases (NCDs) account for over 70% of deaths world-wide. Previous work has linked NCDs such as type 2 diabetes (T2D) to disruption of chromatin regulators. However, the exact molecular origins of these chronic conditions remain elusive. Here, we identify the H4 lysine 16 acetyltransferase MOF as a critical regulator of central carbon metabolism. High-throughput metabolomics unveil a systemic amino acid and carbohydrate imbalance in Mof deficient mice, manifesting in T2D predisposition. Oral glucose tolerance testing (OGTT) reveals defects in glucose assimilation and insulin secretion in these animals. Furthermore, Mof deficient mice are resistant to diet-induced fat gain due to defects in glucose uptake in adipose tissue. MOF-mediated H4K16ac deposition controls expression of the master regulator of glucose metabolism, Pparg and the entire downstream transcriptional network. Glucose uptake and lipid storage can be reconstituted in MOF-depleted adipocytes in vitro by ectopic Glut4 expression, PPARγ agonist thiazolidinedione (TZD) treatment or SIRT1 inhibition. Hence, chronic imbalance in H4K16ac promotes a destabilisation of metabolism triggering the development of a metabolic disorder, and its maintenance provides an unprecedented regulatory epigenetic mechanism controlling diet-induced obesity. Nature Publishing Group UK 2021-10-27 /pmc/articles/PMC8551339/ /pubmed/34707105 http://dx.doi.org/10.1038/s41467-021-26277-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Pessoa Rodrigues, Cecilia Chatterjee, Aindrila Wiese, Meike Stehle, Thomas Szymanski, Witold Shvedunova, Maria Akhtar, Asifa Histone H4 lysine 16 acetylation controls central carbon metabolism and diet-induced obesity in mice |
title | Histone H4 lysine 16 acetylation controls central carbon metabolism and diet-induced obesity in mice |
title_full | Histone H4 lysine 16 acetylation controls central carbon metabolism and diet-induced obesity in mice |
title_fullStr | Histone H4 lysine 16 acetylation controls central carbon metabolism and diet-induced obesity in mice |
title_full_unstemmed | Histone H4 lysine 16 acetylation controls central carbon metabolism and diet-induced obesity in mice |
title_short | Histone H4 lysine 16 acetylation controls central carbon metabolism and diet-induced obesity in mice |
title_sort | histone h4 lysine 16 acetylation controls central carbon metabolism and diet-induced obesity in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551339/ https://www.ncbi.nlm.nih.gov/pubmed/34707105 http://dx.doi.org/10.1038/s41467-021-26277-w |
work_keys_str_mv | AT pessoarodriguescecilia histoneh4lysine16acetylationcontrolscentralcarbonmetabolismanddietinducedobesityinmice AT chatterjeeaindrila histoneh4lysine16acetylationcontrolscentralcarbonmetabolismanddietinducedobesityinmice AT wiesemeike histoneh4lysine16acetylationcontrolscentralcarbonmetabolismanddietinducedobesityinmice AT stehlethomas histoneh4lysine16acetylationcontrolscentralcarbonmetabolismanddietinducedobesityinmice AT szymanskiwitold histoneh4lysine16acetylationcontrolscentralcarbonmetabolismanddietinducedobesityinmice AT shvedunovamaria histoneh4lysine16acetylationcontrolscentralcarbonmetabolismanddietinducedobesityinmice AT akhtarasifa histoneh4lysine16acetylationcontrolscentralcarbonmetabolismanddietinducedobesityinmice |