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Coordinated control of adiposity and growth by anti‐anabolic kinase ERK7
Energy storage and growth are coordinated in response to nutrient status of animals. How nutrient‐regulated signaling pathways control these processes in vivo remains insufficiently understood. Here, we establish an atypical MAP kinase, ERK7, as an inhibitor of adiposity and growth in Drosophila. ER...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7857433/ https://www.ncbi.nlm.nih.gov/pubmed/33369866 http://dx.doi.org/10.15252/embr.201949602 |
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author | Hasygar, Kiran Deniz, Onur Liu, Ying Gullmets, Josef Hynynen, Riikka Ruhanen, Hanna Kokki, Krista Käkelä, Reijo Hietakangas, Ville |
author_facet | Hasygar, Kiran Deniz, Onur Liu, Ying Gullmets, Josef Hynynen, Riikka Ruhanen, Hanna Kokki, Krista Käkelä, Reijo Hietakangas, Ville |
author_sort | Hasygar, Kiran |
collection | PubMed |
description | Energy storage and growth are coordinated in response to nutrient status of animals. How nutrient‐regulated signaling pathways control these processes in vivo remains insufficiently understood. Here, we establish an atypical MAP kinase, ERK7, as an inhibitor of adiposity and growth in Drosophila. ERK7 mutant larvae display elevated triacylglycerol (TAG) stores and accelerated growth rate, while overexpressed ERK7 is sufficient to inhibit lipid storage and growth. ERK7 expression is elevated upon fasting and ERK7 mutant larvae display impaired survival during nutrient deprivation. ERK7 acts in the fat body, the insect counterpart of liver and adipose tissue, where it controls the subcellular localization of chromatin‐binding protein PWP1, a growth‐promoting downstream effector of mTOR. PWP1 maintains the expression of sugarbabe, encoding a lipogenic Gli‐similar family transcription factor. Both PWP1 and Sugarbabe are necessary for the increased growth and adiposity phenotypes of ERK7 loss‐of‐function animals. In conclusion, ERK7 is an anti‐anabolic kinase that inhibits lipid storage and growth while promoting survival on fasting conditions. |
format | Online Article Text |
id | pubmed-7857433 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78574332021-02-05 Coordinated control of adiposity and growth by anti‐anabolic kinase ERK7 Hasygar, Kiran Deniz, Onur Liu, Ying Gullmets, Josef Hynynen, Riikka Ruhanen, Hanna Kokki, Krista Käkelä, Reijo Hietakangas, Ville EMBO Rep Articles Energy storage and growth are coordinated in response to nutrient status of animals. How nutrient‐regulated signaling pathways control these processes in vivo remains insufficiently understood. Here, we establish an atypical MAP kinase, ERK7, as an inhibitor of adiposity and growth in Drosophila. ERK7 mutant larvae display elevated triacylglycerol (TAG) stores and accelerated growth rate, while overexpressed ERK7 is sufficient to inhibit lipid storage and growth. ERK7 expression is elevated upon fasting and ERK7 mutant larvae display impaired survival during nutrient deprivation. ERK7 acts in the fat body, the insect counterpart of liver and adipose tissue, where it controls the subcellular localization of chromatin‐binding protein PWP1, a growth‐promoting downstream effector of mTOR. PWP1 maintains the expression of sugarbabe, encoding a lipogenic Gli‐similar family transcription factor. Both PWP1 and Sugarbabe are necessary for the increased growth and adiposity phenotypes of ERK7 loss‐of‐function animals. In conclusion, ERK7 is an anti‐anabolic kinase that inhibits lipid storage and growth while promoting survival on fasting conditions. John Wiley and Sons Inc. 2020-12-28 2021-02-03 /pmc/articles/PMC7857433/ /pubmed/33369866 http://dx.doi.org/10.15252/embr.201949602 Text en © 2020 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Hasygar, Kiran Deniz, Onur Liu, Ying Gullmets, Josef Hynynen, Riikka Ruhanen, Hanna Kokki, Krista Käkelä, Reijo Hietakangas, Ville Coordinated control of adiposity and growth by anti‐anabolic kinase ERK7 |
title | Coordinated control of adiposity and growth by anti‐anabolic kinase ERK7 |
title_full | Coordinated control of adiposity and growth by anti‐anabolic kinase ERK7 |
title_fullStr | Coordinated control of adiposity and growth by anti‐anabolic kinase ERK7 |
title_full_unstemmed | Coordinated control of adiposity and growth by anti‐anabolic kinase ERK7 |
title_short | Coordinated control of adiposity and growth by anti‐anabolic kinase ERK7 |
title_sort | coordinated control of adiposity and growth by anti‐anabolic kinase erk7 |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7857433/ https://www.ncbi.nlm.nih.gov/pubmed/33369866 http://dx.doi.org/10.15252/embr.201949602 |
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