An RNA-seq atlas of mouse brain areas during fasting and diet-induced obesity

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Mammalian energy homeostasis is primarilly regulated by the hypothalamus and hindbrain, with the hippocampus, midbrain nuclei, and other regions implicated by evidence from human genetics studies. To understand how these non-canonical brain regions respond to imbalances in energy homeostasis, we performed two experiments examining the effects of different diets in male C57BL6 mice. In our first study, groups of six pair-housed mice were given access to chow, high-fat diet or fasted for 16 hours. In our subsequent study, two groups of 10 mice were single-housed and given access to chow or fasted for 24 h. We recorded food intake for each cage, the change in body weight for each animal, and collected hypothalamus, hippocampus, superior colliculus, inferior colliculus, frontal cortex, and zona incerta-centric samples. We performed bulk RNA sequencing on 185 samples and validated them by a series of quality control assessments including alignment quality and gene expression profiling. We believe these studies capture the transcriptomic effects of acute fasting and high-fat diet in the rodent brain and provide a valuable reference.

OriginalsprogEngelsk
Artikelnummer44
TidsskriftScientific Data
Vol/bind11
Antal sider8
ISSN2052-4463
DOI
StatusUdgivet - 2024

Bibliografisk note

Funding Information:
The authors are grateful for the technical assistance provided by Helle Kinggaard Lilja-Fischer at the University of Copenhagen. We acknowledge The Single-Cell Omics platform at the Novo Nordisk Foundation Center for Basic Metabolic Research (CBMR) and Lars Roed Ingerslev for the technical expertise and support. CBMR is an independent Research Center, based at the University of Copenhagen and partially funded by an unconditional donation from the Novo Nordisk Foundation ( https://cbmr.ku.dk/ ; grant no. NNF18CC0034900). T.H.P. was supported by grants from the Novo Nordisk Foundation (NNF16OC0021496) and Lundbeck Foundation (R19020143904). C.C. is supported by research grants from the Lundbeck Foundation (Fellowship R238-2016-2859) and the Novo Nordisk Foundation (grant numbers NNF17OC0026114). P.V.T. was supported by the Novo Nordisk Foundation (NNF18CC0033668).

Publisher Copyright:
© 2024, The Author(s).

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