Senyilmaz 2015 Nature: Difference between revisions
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{{Publication | {{Publication | ||
|title=Senyilmaz D, Virtue S, Xu X, Tan CY, Griffin JL, Miller AK, Vidal-Puig A, Teleman AA (2015) Regulation of mitochondrial morphology and function by stearoylation of TFR1. Nature | |title=Senyilmaz D, Virtue S, Xu X, Tan CY, Griffin JL, Miller AK, Vidal-Puig A, Teleman AA (2015) Regulation of mitochondrial morphology and function by stearoylation of TFR1. Nature 525:124-8. | ||
|info=[http://www.ncbi.nlm.nih.gov/pubmed/26214738 PMID: 26214738] | |info=[http://www.ncbi.nlm.nih.gov/pubmed/26214738 PMID: 26214738] | ||
|authors=Senyilmaz D, Virtue S, Xu X, Tan CY, Griffin JL, Miller AK, Vidal-Puig A, Teleman AA | |authors=Senyilmaz D, Virtue S, Xu X, Tan CY, Griffin JL, Miller AK, Vidal-Puig A, Teleman AA | ||
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|journal=Nature | |journal=Nature | ||
|abstract=Mitochondria are involved in a variety of cellular functions, including ATP production, amino acid and lipid biogenesis and breakdown, signalling and apoptosis. Mitochondrial dysfunction has been linked to neurodegenerative diseases, cancer and ageing. Although transcriptional mechanisms that regulate mitochondrial abundance are known, comparatively little is known about how mitochondrial function is regulated. Here we identify the metabolite stearic acid (C18:0) and human transferrin receptor 1 (TFR1; also known as TFRC) as mitochondrial regulators. We elucidate a signalling pathway whereby C18:0 stearoylates TFR1, thereby inhibiting its activation of JNK signalling. This leads to reduced ubiquitination of mitofusin via HUWE1, thereby promoting mitochondrial fusion and function. We find that animal cells are poised to respond to both increases and decreases in C18:0 levels, with increased C18:0 dietary intake boosting mitochondrial fusion ''in vivo''. Intriguingly, dietary C18:0 supplementation can counteract the mitochondrial dysfunction caused by genetic defects such as loss of the Parkinson's disease genes ''Pink'' or ''Parkin'' in ''Drosophila''. This work identifies the metabolite C18:0 as a signalling molecule regulating mitochondrial function in response to diet. | |abstract=Mitochondria are involved in a variety of cellular functions, including ATP production, amino acid and lipid biogenesis and breakdown, signalling and apoptosis. Mitochondrial dysfunction has been linked to neurodegenerative diseases, cancer and ageing. Although transcriptional mechanisms that regulate mitochondrial abundance are known, comparatively little is known about how mitochondrial function is regulated. Here we identify the metabolite stearic acid (C18:0) and human transferrin receptor 1 (TFR1; also known as TFRC) as mitochondrial regulators. We elucidate a signalling pathway whereby C18:0 stearoylates TFR1, thereby inhibiting its activation of JNK signalling. This leads to reduced ubiquitination of mitofusin via HUWE1, thereby promoting mitochondrial fusion and function. We find that animal cells are poised to respond to both increases and decreases in C18:0 levels, with increased C18:0 dietary intake boosting mitochondrial fusion ''in vivo''. Intriguingly, dietary C18:0 supplementation can counteract the mitochondrial dysfunction caused by genetic defects such as loss of the Parkinson's disease genes ''Pink'' or ''Parkin'' in ''Drosophila''. This work identifies the metabolite C18:0 as a signalling molecule regulating mitochondrial function in response to diet. | ||
|mipnetlab=DE Heidelberg Teleman A | |||
}} | }} | ||
{{Labeling | {{Labeling | ||
|area=Respiration, mt-Structure;fission;fusion, mtDNA;mt-genetics, nDNA;cell genetics, Genetic knockout;overexpression, Exercise physiology;nutrition;life style, mt-Awareness | |area=Respiration, mt-Structure;fission;fusion, mtDNA;mt-genetics, nDNA;cell genetics, Genetic knockout;overexpression, Exercise physiology;nutrition;life style, mt-Awareness | ||
|diseases=Parkinson's | |||
|organism=Drosophila | |organism=Drosophila | ||
|preparations=Permeabilized tissue | |preparations=Permeabilized tissue | ||
|enzymes=Complex IV;cytochrome c oxidase | |enzymes=Complex IV;cytochrome c oxidase | ||
|topics=Fatty acid | |topics=Fatty acid | ||
|couplingstates=OXPHOS, | |couplingstates=OXPHOS, ET | ||
| | |pathways=N, S, CIV, NS | ||
|instruments=Oxygraph-2k | |instruments=Oxygraph-2k | ||
}} | }} | ||
Latest revision as of 10:53, 27 March 2018
| Senyilmaz D, Virtue S, Xu X, Tan CY, Griffin JL, Miller AK, Vidal-Puig A, Teleman AA (2015) Regulation of mitochondrial morphology and function by stearoylation of TFR1. Nature 525:124-8. |
Senyilmaz D, Virtue S, Xu X, Tan CY, Griffin JL, Miller AK, Vidal-Puig A, Teleman AA (2015) Nature
Abstract: Mitochondria are involved in a variety of cellular functions, including ATP production, amino acid and lipid biogenesis and breakdown, signalling and apoptosis. Mitochondrial dysfunction has been linked to neurodegenerative diseases, cancer and ageing. Although transcriptional mechanisms that regulate mitochondrial abundance are known, comparatively little is known about how mitochondrial function is regulated. Here we identify the metabolite stearic acid (C18:0) and human transferrin receptor 1 (TFR1; also known as TFRC) as mitochondrial regulators. We elucidate a signalling pathway whereby C18:0 stearoylates TFR1, thereby inhibiting its activation of JNK signalling. This leads to reduced ubiquitination of mitofusin via HUWE1, thereby promoting mitochondrial fusion and function. We find that animal cells are poised to respond to both increases and decreases in C18:0 levels, with increased C18:0 dietary intake boosting mitochondrial fusion in vivo. Intriguingly, dietary C18:0 supplementation can counteract the mitochondrial dysfunction caused by genetic defects such as loss of the Parkinson's disease genes Pink or Parkin in Drosophila. This work identifies the metabolite C18:0 as a signalling molecule regulating mitochondrial function in response to diet.
• O2k-Network Lab: DE Heidelberg Teleman A
Labels: MiParea: Respiration, mt-Structure;fission;fusion, mtDNA;mt-genetics, nDNA;cell genetics, Genetic knockout;overexpression, Exercise physiology;nutrition;life style, mt-Awareness
Pathology: Parkinson's
Organism: Drosophila
Preparation: Permeabilized tissue Enzyme: Complex IV;cytochrome c oxidase Regulation: Fatty acid Coupling state: OXPHOS, ET Pathway: N, S, CIV, NS HRR: Oxygraph-2k
