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Human METTL12 is a mitochondrial methyltransferase that modifies citrate synthase

Published version
Peer-reviewed

Type

Article

Change log

Authors

Rhein, VF 
Carroll, J 
Ding, S 
Fearnley, IM 
Walker, JE 

Abstract

The protein methylome in mammalian mitochondria has been little studied until recently. Here, we describe that lysine-368 of human citrate synthase is methylated and that the modifying enzyme, localized in the mitochondrial matrix, is methyltransferase-like protein 12 (METTL12), a member of the family of 7β-strand methyltransferases. Lysine-368 is near the active site of citrate synthase, but removal of methylation has no effect on its activity. In mitochondria, it is possible that some or all of the enzymes of the citric acid cycle, including citrate synthase, are organized in metabolons to facilitate the channelling of substrates between participating enzymes. Thus, possible roles for the methylation of Lys-368 are in controlling substrate channelling itself, or in influencing protein–protein interactions in the metabolon.

Description

Keywords

citrate synthase, metabolons, METTL12, mitochondria, protein methylation, substrate channelling

Journal Title

FEBS Letters

Conference Name

Journal ISSN

0014-5793
1873-3468

Volume Title

591

Publisher

Elsevier
Sponsorship
Medical Research Council (MC_EX_MR/M009858/1)
Medical Research Council (MC_U105663150)
Medical Research Council (MC_UU_00015/8)
MRC (MC_UU_00015/8)
Medical Research Council (MC_UU_00015/7)
This work was supported by the Medical Research Council of the United Kingdom by grant MC_U1065663150 and by Programme Grant MR/M009858/1, both to JEW and a Fellowship from the Swiss Novartis Foundation to VFR.