Methionine Adenosyltransferase α1 Is Targeted to the Mitochondrial Matrix and Interacts with Cytochrome P450 2E1 to Lower Its Expression

dc.contributor.authorMurray, Ben
dc.contributor.authorPeng, Hui
dc.contributor.authorBarbier-Torres, Lucia
dc.contributor.authorRobinson, Aaron
dc.contributor.authorLi, Tony W. H.
dc.contributor.authorFan, Wei
dc.contributor.authorTomasi, Maria Lauda
dc.contributor.authorGottlieb, Roberta A.
dc.contributor.authorVan Eyk, Jenny
dc.contributor.authorLu, Zhimin
dc.contributor.authorMartínez-Chantar, M. L.
dc.contributor.authorLiangpunsakul, Suthat
dc.contributor.authorSkill, Nicholas J.
dc.contributor.authorMato, José M.
dc.contributor.authorLu, Shelly C.
dc.contributor.departmentMedicine, School of Medicineen_US
dc.date.accessioned2019-08-15T16:55:09Z
dc.date.available2019-08-15T16:55:09Z
dc.date.issued2019
dc.description.abstractMethionine adenosyltransferase α1 (MATα1, encoded by MAT1A) is responsible for hepatic biosynthesis of S‐adenosyl methionine, the principal methyl donor. MATα1 also act as a transcriptional cofactor by interacting and influencing the activity of several transcription factors. Mat1a knockout (KO) mice have increased levels of cytochrome P450 2E1 (CYP2E1), but the underlying mechanisms are unknown. The aims of the current study were to identify binding partners of MATα1 and elucidate how MATα1 regulates CYP2E1 expression. We identified binding partners of MATα1 by coimmunoprecipitation (co‐IP) and mass spectrometry. Interacting proteins were confirmed using co‐IP using recombinant proteins, liver lysates, and mitochondria. Alcoholic liver disease (ALD) samples were used to confirm relevance of our findings. We found that MATα1 negatively regulates CYP2E1 at mRNA and protein levels, with the latter being the dominant mechanism. MATα1 interacts with many proteins but with a predominance of mitochondrial proteins including CYP2E1. We found that MATα1 is present in the mitochondrial matrix of hepatocytes using immunogold electron microscopy. Mat1a KO hepatocytes had reduced mitochondrial membrane potential and higher mitochondrial reactive oxygen species, both of which were normalized when MAT1A was overexpressed. In addition, KO hepatocytes were sensitized to ethanol and tumor necrosis factor α–induced mitochondrial dysfunction. Interaction of MATα1 with CYP2E1 was direct, and this facilitated CYP2E1 methylation at R379, leading to its degradation through the proteasomal pathway. Mat1a KO livers have a reduced methylated/total CYP2E1 ratio. MATα1’s influence on mitochondrial function is largely mediated by its effect on CYP2E1 expression. Patients with ALD have reduced MATα1 levels and a decrease in methylated/total CYP2E1 ratio. Conclusion: Our findings highlight a critical role of MATα1 in regulating mitochondrial function by suppressing CYP2E1 expression at multiple levels.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationMurray, B., Peng, H., Barbier‐Torres, L., Robinson, A., Li, T. W. H., Fan, W., … Lu, S. C. (2019). Methionine Adenosyltransferase α1 is targeted to the mitochondrial matrix and interacts with cytochrome P450 2E1 to lower its expression. Hepatology, 0(ja). https://doi.org/10.1002/hep.30762en_US
dc.identifier.urihttps://hdl.handle.net/1805/20385
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.isversionof10.1002/hep.30762en_US
dc.relation.journalHepatologyen_US
dc.rightsPublisher Policyen_US
dc.sourceAuthoren_US
dc.subjectmitochondrial functionen_US
dc.subjectS-adenosylmethionineen_US
dc.subjectmethylationen_US
dc.titleMethionine Adenosyltransferase α1 Is Targeted to the Mitochondrial Matrix and Interacts with Cytochrome P450 2E1 to Lower Its Expressionen_US
dc.typeArticleen_US
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