Mitochondrial fatty acid synthesis coordinates mitochondrial oxidative metabolism
Ontology highlight
ABSTRACT:
PROVIDER: PRJNA625208 | ENA |
REPOSITORIES: ENA
Dataset's files
| Action | DRS | |||
|---|---|---|---|---|
| SRR11541400_1.fastq.gz | Fastqsanger.gz | |||
| SRR11541400_2.fastq.gz | Fastqsanger.gz | |||
| SRR11541401_1.fastq.gz | Fastqsanger.gz | |||
| SRR11541401_2.fastq.gz | Fastqsanger.gz | |||
| SRR11541402_1.fastq.gz | Fastqsanger.gz |
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Project description:Cells harbor two systems for fatty acid synthesis, one in the cytoplasm (catalyzed by fatty acid synthase, FASN) and one in the mitochondria (mtFAS). In contrast to FASN, mtFAS is poorly characterized, especially in higher eukaryotes, with the major product(s), metabolic roles, and cellular function(s) being essentially unknown. Here we show that hypomorphic mtFAS mutant mouse skeletal myoblast cell lines display a severe loss of electron transport chain (ETC) complexes and exhibit compensatory metabolic activities including reductive carboxylation. This effect on ETC complexes appears to be independent of protein lipoylation, the best characterized function of mtFAS, as mutants lacking lipoylation have an intact ETC. Finally, mtFAS impairment blocks the differentiation of skeletal myoblasts in vitro. Together, these data suggest that ETC activity in mammals is profoundly controlled by mtFAS function, thereby connecting anabolic fatty acid synthesis with the oxidation of carbon fuels.
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