<i>METTL3</i> and <i>FTO</i> Regulate Heat Stress Response in Hu Sheep Through Lipid Metabolism via m6A Modification

In an established hepatocyte lipid deposition heat stress model, the expression levels of <i>METTL3</i> and <i>FTO</i> were significantly upregulated (<i>p</i> < 0.05), indicating that <i>METTL3</i> and <i>FTO</i> play important roles in...

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Main Authors: Bowen Chen, Chao Yuan, Tingting Guo, Jianbin Liu, Zengkui Lu
Format: Article
Language:English
Published: MDPI AG 2025-01-01
Series:Animals
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Online Access:https://www.mdpi.com/2076-2615/15/2/193
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author Bowen Chen
Chao Yuan
Tingting Guo
Jianbin Liu
Zengkui Lu
author_facet Bowen Chen
Chao Yuan
Tingting Guo
Jianbin Liu
Zengkui Lu
author_sort Bowen Chen
collection DOAJ
description In an established hepatocyte lipid deposition heat stress model, the expression levels of <i>METTL3</i> and <i>FTO</i> were significantly upregulated (<i>p</i> < 0.05), indicating that <i>METTL3</i> and <i>FTO</i> play important roles in the process of lipid deposition heat stress in hepatocytes. Transcriptome and metabolome analyses showed that lipid deposition heat stress had significant effects on the linoleic acid, linolenic acid, glycerophospholipid, and arachidonic acid metabolic pathways in hepatocytes. After <i>METTL3</i> knockdown, the m6A methylation level decreased, but the difference was not significant (<i>p</i> > 0.05), the <i>FABP4</i> and <i>Accα</i> expression levels increased, and the <i>HSP60</i>, <i>HSP70</i>, and <i>HSP110</i> expression levels decreased significantly. After <i>METTL3</i> overexpression, the m6A methylation level increased significantly and the expression levels of <i>FABP4</i>, <i>ATGL</i>, <i>Accα</i>, <i>HSP60</i>, <i>HSP70</i>, <i>HSP90</i>, and <i>HSP110</i> decreased significantly, indicating that the overexpression of <i>METTL3</i> reduced the expression of heat shock genes by inhibiting the lipid-deposition-related gene expression in an m6A-dependent manner. The m6A methylation level increased significantly after <i>FTO</i> knockdown, while <i>HSP60</i>, <i>HSP110</i>, <i>FABP4</i>, <i>ATGL</i>, and Accα expression levels were significantly reduced. Following <i>FTO</i> overexpression, the m6A methylation level and <i>HSP60</i>, <i>HSP90</i>, and <i>HSP110</i> expression levels significantly decreased, while the <i>ATGL</i> and <i>Accα</i> expression levels significantly increased. This indicates that the overexpression of <i>FTO</i> promoted the expression of lipid-deposition-related genes in an m6A-dependent manner to reduce the expression of heat shock genes. Transcriptome and metabolome sequencing screened a large number of differential genes and metabolites, and a KEGG enrichment analysis showed that m6A methylation mainly regulated heat stress by affecting the TNF, cAMP, MAPK, lipolysis, and synthesis pathways in hepatocytes. In the lipid deposition heat stress model of preadipocytes, the regulation of gene expression was similar to that in hepatocytes.
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spelling doaj-art-dbffd5cced944e9099109f4f16f76c612025-01-24T13:18:00ZengMDPI AGAnimals2076-26152025-01-0115219310.3390/ani15020193<i>METTL3</i> and <i>FTO</i> Regulate Heat Stress Response in Hu Sheep Through Lipid Metabolism via m6A ModificationBowen Chen0Chao Yuan1Tingting Guo2Jianbin Liu3Zengkui Lu4Key Laboratory of Animal Genetics and Breeding on Tibetan Plateau, Ministry of Agriculture and Rural Affairs, Lanzhou Institute of Husbandry and Pharmaceutical Sciences, Chinese Academy of Agricultural Sciences, Lanzhou 730050, ChinaKey Laboratory of Animal Genetics and Breeding on Tibetan Plateau, Ministry of Agriculture and Rural Affairs, Lanzhou Institute of Husbandry and Pharmaceutical Sciences, Chinese Academy of Agricultural Sciences, Lanzhou 730050, ChinaKey Laboratory of Animal Genetics and Breeding on Tibetan Plateau, Ministry of Agriculture and Rural Affairs, Lanzhou Institute of Husbandry and Pharmaceutical Sciences, Chinese Academy of Agricultural Sciences, Lanzhou 730050, ChinaKey Laboratory of Animal Genetics and Breeding on Tibetan Plateau, Ministry of Agriculture and Rural Affairs, Lanzhou Institute of Husbandry and Pharmaceutical Sciences, Chinese Academy of Agricultural Sciences, Lanzhou 730050, ChinaKey Laboratory of Animal Genetics and Breeding on Tibetan Plateau, Ministry of Agriculture and Rural Affairs, Lanzhou Institute of Husbandry and Pharmaceutical Sciences, Chinese Academy of Agricultural Sciences, Lanzhou 730050, ChinaIn an established hepatocyte lipid deposition heat stress model, the expression levels of <i>METTL3</i> and <i>FTO</i> were significantly upregulated (<i>p</i> < 0.05), indicating that <i>METTL3</i> and <i>FTO</i> play important roles in the process of lipid deposition heat stress in hepatocytes. Transcriptome and metabolome analyses showed that lipid deposition heat stress had significant effects on the linoleic acid, linolenic acid, glycerophospholipid, and arachidonic acid metabolic pathways in hepatocytes. After <i>METTL3</i> knockdown, the m6A methylation level decreased, but the difference was not significant (<i>p</i> > 0.05), the <i>FABP4</i> and <i>Accα</i> expression levels increased, and the <i>HSP60</i>, <i>HSP70</i>, and <i>HSP110</i> expression levels decreased significantly. After <i>METTL3</i> overexpression, the m6A methylation level increased significantly and the expression levels of <i>FABP4</i>, <i>ATGL</i>, <i>Accα</i>, <i>HSP60</i>, <i>HSP70</i>, <i>HSP90</i>, and <i>HSP110</i> decreased significantly, indicating that the overexpression of <i>METTL3</i> reduced the expression of heat shock genes by inhibiting the lipid-deposition-related gene expression in an m6A-dependent manner. The m6A methylation level increased significantly after <i>FTO</i> knockdown, while <i>HSP60</i>, <i>HSP110</i>, <i>FABP4</i>, <i>ATGL</i>, and Accα expression levels were significantly reduced. Following <i>FTO</i> overexpression, the m6A methylation level and <i>HSP60</i>, <i>HSP90</i>, and <i>HSP110</i> expression levels significantly decreased, while the <i>ATGL</i> and <i>Accα</i> expression levels significantly increased. This indicates that the overexpression of <i>FTO</i> promoted the expression of lipid-deposition-related genes in an m6A-dependent manner to reduce the expression of heat shock genes. Transcriptome and metabolome sequencing screened a large number of differential genes and metabolites, and a KEGG enrichment analysis showed that m6A methylation mainly regulated heat stress by affecting the TNF, cAMP, MAPK, lipolysis, and synthesis pathways in hepatocytes. In the lipid deposition heat stress model of preadipocytes, the regulation of gene expression was similar to that in hepatocytes.https://www.mdpi.com/2076-2615/15/2/193m6A methylation<i>METTL3</i><i>FTO</i>heat stresslipid metabolismsheep
spellingShingle Bowen Chen
Chao Yuan
Tingting Guo
Jianbin Liu
Zengkui Lu
<i>METTL3</i> and <i>FTO</i> Regulate Heat Stress Response in Hu Sheep Through Lipid Metabolism via m6A Modification
Animals
m6A methylation
<i>METTL3</i>
<i>FTO</i>
heat stress
lipid metabolism
sheep
title <i>METTL3</i> and <i>FTO</i> Regulate Heat Stress Response in Hu Sheep Through Lipid Metabolism via m6A Modification
title_full <i>METTL3</i> and <i>FTO</i> Regulate Heat Stress Response in Hu Sheep Through Lipid Metabolism via m6A Modification
title_fullStr <i>METTL3</i> and <i>FTO</i> Regulate Heat Stress Response in Hu Sheep Through Lipid Metabolism via m6A Modification
title_full_unstemmed <i>METTL3</i> and <i>FTO</i> Regulate Heat Stress Response in Hu Sheep Through Lipid Metabolism via m6A Modification
title_short <i>METTL3</i> and <i>FTO</i> Regulate Heat Stress Response in Hu Sheep Through Lipid Metabolism via m6A Modification
title_sort i mettl3 i and i fto i regulate heat stress response in hu sheep through lipid metabolism via m6a modification
topic m6A methylation
<i>METTL3</i>
<i>FTO</i>
heat stress
lipid metabolism
sheep
url https://www.mdpi.com/2076-2615/15/2/193
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AT tingtingguo imettl3iandiftoiregulateheatstressresponseinhusheepthroughlipidmetabolismviam6amodification
AT jianbinliu imettl3iandiftoiregulateheatstressresponseinhusheepthroughlipidmetabolismviam6amodification
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