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RNA sequencing screening and gene function analysis uncover G protein-coupled receptor 183 as a key mediator for methionine to stimulate milk synthesis in mouse mammary epithelial cells

Published online by Cambridge University Press:  04 June 2024

Yuwen Zhou
Affiliation:
College of Animal Science and Technology, Yangtze University, Jingzhou 434025, People’s Republic of China
Sihua Fan
Affiliation:
College of Animal Science and Technology, Yangtze University, Jingzhou 434025, People’s Republic of China
Ming Xu
Affiliation:
College of Animal Science and Technology, Yangtze University, Jingzhou 434025, People’s Republic of China
Minghui Zhang
Affiliation:
College of Animal Science and Technology, Yangtze University, Jingzhou 434025, People’s Republic of China
Xuejun Gao*
Affiliation:
College of Animal Science and Technology, Yangtze University, Jingzhou 434025, People’s Republic of China
*
*Corresponding author: Xuejun Gao, email gaoxj53901@163.com

Abstract

Methionine (Met) can activate the mechanistic target of rapamycin (mTOR) to promote milk synthesis in mammary epithelial cells. However, it is largely unknown which G protein-coupled receptor can mediate the stimulation of Met on mTOR activation. In this study, we employed transcriptome sequencing to analyse which G protein-coupled receptors were associated with the role of Met and further used gene function study approaches to explore the role of G protein-coupled receptor 183 (GPR183) in Met stimulation on mTOR activation in HC11 cells. We identified nine G protein-coupled receptors including GPR183 whose expression levels were upregulated by Met treatment through RNA sequencing and subsequent quantitative real-time PCR analysis. Using GPR183 knockdown and overexpression technology, we demonstrate that GPR183 is a positive regulator of milk protein and fat synthesis and proliferation of HC11 cells. Met affected GPR183 expression in a dose-dependent manner, and GPR183 mediated the stimulation of Met (0·6 mM) on milk protein and fat synthesis, cell proliferation and mTOR phosphorylation and mRNA expression. The inhibition of phosphoinositide 3-kinase blocked the phosphorylation of mTOR and AKT stimulated by GPR183 activation. In summary, through RNA sequencing and gene function study, we uncover that GPR183 is a key mediator for Met to activate the phosphoinositide 3-kinase-mTOR signalling and milk synthesis in mouse mammary epithelial cells.

Type
Research Article
Copyright
© The Author(s), 2024. Published by Cambridge University Press on behalf of The Nutrition Society

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