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Gene expression profiles of PGAM5-knockout brown adipose tissue

ABSTRACT: Gene expression profiles of PGAM5-knockout brown adipose tissue

PROVIDER: PRJNA577125 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR10267867_1.fastq.gz	Fastqsanger.gz
	SRR10267867_2.fastq.gz	Fastqsanger.gz
	SRR10267868_1.fastq.gz	Fastqsanger.gz
	SRR10267868_2.fastq.gz	Fastqsanger.gz
	SRR10267869_1.fastq.gz	Fastqsanger.gz

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Gene expression profiles of PGAM5-knockout brown adipose tissue

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Project description:Uncovering the role of upstream ORFs (uORFs) challenges conventional views of one protein per mRNA while also revealing the capacity of some uORFs to encode microproteins that contribute to cellular biology and physiology. This study explores the functional role of a recently identified mitochondrial microprotein, SLC35A4-MP, in the brown adipose tissue of mice. Our findings reveal dynamic regulation of SLC35A4-MP expression during primary brown adipocyte differentiation in vitro and during cold exposure or high-fat diet (HFD)-induced obesity in mice. Using a knockout mouse model, we show that loss of SLC35A4-MP disrupts mitochondrial lipid composition, decreasing cardiolipins and phosphatidylethanolamine in brown adipose tissue from HFD-fed mice. SLC35A4-MP deficiency also impairs mitochondrial activity, alters mitochondrial number and morphology, and promotes inflammation. For example, knockout mice accumulate acylcarnitines during cold exposure, indicating defective fatty acid oxidation. These findings reveal SLC35A4-MP as a previously unrecognized microprotein in the endogenous regulation of mitochondrial function and tissue lipid metabolism, adding to the growing list of functional endogenous microproteins

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