The novel conserved mitochondrial inner-membrane protein MTGM regulates mitochondrial morphology and cell proliferation
Dynamins
0301 basic medicine
Brain Neoplasms
Cell Cycle
Molecular Sequence Data
Intracellular Signaling Peptides and Proteins
Membrane Proteins
Apoptosis
GTP Phosphohydrolases
Mitochondria
Mitochondrial Proteins
03 medical and health sciences
Cell Line, Tumor
Mitochondrial Membranes
Autophagy
Animals
Humans
RNA, Small Interfering
Apoptosis Regulatory Proteins
Microtubule-Associated Proteins
Cell Proliferation
DOI:
10.1242/jcs.038513
Publication Date:
2009-06-17T19:03:57Z
AUTHORS (8)
ABSTRACT
Although several proteins involved in mediating mitochondrial division have been reported in mammals, the mechanism of the fission machinery remains to be elucidated. Here, we identified a human nuclear gene (named MTGM) that encodes a novel, small, integral mitochondrial inner-membrane protein and shows high expression in both human brain tumor cell lines and tumor tissues. The gene is evolutionarily highly conserved, and its orthologs are 100% identical at the amino acid level in all analyzed mammalian species. The gene product is characterized by an unusual tetrad of the GxxxG motif in the transmembrane segment. Overexpression of MTGM (mitochondrial targeting GxxxG motif) protein results in mitochondrial fragmentation and release of mitochondrial Smac/Diablo to the cytosol with no effect on apoptosis. MTGM-induced mitochondrial fission can be blocked by a dominant negative Drp1 mutant (Drp1-K38A). Overexpression of MTGM also results in inhibition of cell proliferation, stalling of cells in S phase and nuclear accumulation of γ-H2AX. Knockdown of MTGM by RNA interference induces mitochondrial elongation, an increase of cell proliferation and inhibition of cell death induced by apoptotic stimuli. In conclusion, we suggest that MTGM is an integral mitochondrial inner-membrane protein that coordinately regulates mitochondrial morphology and cell proliferation.
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