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The long noncoding RNA ADIPINT regulates human adipocyte metabolism via pyruvate carboxylase
The pleiotropic function of long noncoding RNAs is well recognized, but their direct role in governing metabolic homeostasis is less understood. Here, we describe a human adipocyte-specific lncRNA, ADIPINT, that regulates pyruvate carboxylase, a pivotal enzyme in energy metabolism. We developed an a...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9135762/ https://www.ncbi.nlm.nih.gov/pubmed/35618718 http://dx.doi.org/10.1038/s41467-022-30620-0 |
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author | Kerr, Alastair G. Wang, Zuoneng Wang, Na Kwok, Kelvin H. M. Jalkanen, Jutta Ludzki, Alison Lecoutre, Simon Langin, Dominique Bergo, Martin O. Dahlman, Ingrid Mim, Carsten Arner, Peter Gao, Hui |
author_facet | Kerr, Alastair G. Wang, Zuoneng Wang, Na Kwok, Kelvin H. M. Jalkanen, Jutta Ludzki, Alison Lecoutre, Simon Langin, Dominique Bergo, Martin O. Dahlman, Ingrid Mim, Carsten Arner, Peter Gao, Hui |
author_sort | Kerr, Alastair G. |
collection | PubMed |
description | The pleiotropic function of long noncoding RNAs is well recognized, but their direct role in governing metabolic homeostasis is less understood. Here, we describe a human adipocyte-specific lncRNA, ADIPINT, that regulates pyruvate carboxylase, a pivotal enzyme in energy metabolism. We developed an approach, Targeted RNA-protein identification using Orthogonal Organic Phase Separation, which identifies that ADIPINT binds to pyruvate carboxylase and validated the interaction with electron microscopy. ADIPINT knockdown alters the interactome and decreases the abundance and enzymatic activity of pyruvate carboxylase in the mitochondria. Reduced ADIPINT or pyruvate carboxylase expression lowers adipocyte lipid synthesis, breakdown, and lipid content. In human white adipose tissue, ADIPINT expression is increased in obesity and linked to fat cell size, adipose insulin resistance, and pyruvate carboxylase activity. Thus, we identify ADIPINT as a regulator of lipid metabolism in human white adipocytes, which at least in part is mediated through its interaction with pyruvate carboxylase. |
format | Online Article Text |
id | pubmed-9135762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91357622022-05-28 The long noncoding RNA ADIPINT regulates human adipocyte metabolism via pyruvate carboxylase Kerr, Alastair G. Wang, Zuoneng Wang, Na Kwok, Kelvin H. M. Jalkanen, Jutta Ludzki, Alison Lecoutre, Simon Langin, Dominique Bergo, Martin O. Dahlman, Ingrid Mim, Carsten Arner, Peter Gao, Hui Nat Commun Article The pleiotropic function of long noncoding RNAs is well recognized, but their direct role in governing metabolic homeostasis is less understood. Here, we describe a human adipocyte-specific lncRNA, ADIPINT, that regulates pyruvate carboxylase, a pivotal enzyme in energy metabolism. We developed an approach, Targeted RNA-protein identification using Orthogonal Organic Phase Separation, which identifies that ADIPINT binds to pyruvate carboxylase and validated the interaction with electron microscopy. ADIPINT knockdown alters the interactome and decreases the abundance and enzymatic activity of pyruvate carboxylase in the mitochondria. Reduced ADIPINT or pyruvate carboxylase expression lowers adipocyte lipid synthesis, breakdown, and lipid content. In human white adipose tissue, ADIPINT expression is increased in obesity and linked to fat cell size, adipose insulin resistance, and pyruvate carboxylase activity. Thus, we identify ADIPINT as a regulator of lipid metabolism in human white adipocytes, which at least in part is mediated through its interaction with pyruvate carboxylase. Nature Publishing Group UK 2022-05-26 /pmc/articles/PMC9135762/ /pubmed/35618718 http://dx.doi.org/10.1038/s41467-022-30620-0 Text en © The Author(s) 2022 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 Kerr, Alastair G. Wang, Zuoneng Wang, Na Kwok, Kelvin H. M. Jalkanen, Jutta Ludzki, Alison Lecoutre, Simon Langin, Dominique Bergo, Martin O. Dahlman, Ingrid Mim, Carsten Arner, Peter Gao, Hui The long noncoding RNA ADIPINT regulates human adipocyte metabolism via pyruvate carboxylase |
title | The long noncoding RNA ADIPINT regulates human adipocyte metabolism via pyruvate carboxylase |
title_full | The long noncoding RNA ADIPINT regulates human adipocyte metabolism via pyruvate carboxylase |
title_fullStr | The long noncoding RNA ADIPINT regulates human adipocyte metabolism via pyruvate carboxylase |
title_full_unstemmed | The long noncoding RNA ADIPINT regulates human adipocyte metabolism via pyruvate carboxylase |
title_short | The long noncoding RNA ADIPINT regulates human adipocyte metabolism via pyruvate carboxylase |
title_sort | long noncoding rna adipint regulates human adipocyte metabolism via pyruvate carboxylase |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9135762/ https://www.ncbi.nlm.nih.gov/pubmed/35618718 http://dx.doi.org/10.1038/s41467-022-30620-0 |
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