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The dynamin-related GTPase, Mgm1p, is an intermembrane space protein required for maintenance of fusion competent mitochondria.

Wong ED, Wagner JA, Gorsich SW, McCaffery JM, Shaw JM, Nunnari J - J. Cell Biol. (2000)

Bottom Line: To study the primary function of MGM1, we characterized new temperature sensitive MGM1 alleles.Although Mgm1p was recently reported to localize to the mitochondrial outer membrane, our studies indicate that Mgm1p is localized to the mitochondrial intermembrane space.Based on our localization data and Mgm1p's structural homology to dynamin, we postulate that it functions in inner membrane remodeling events.

View Article: PubMed Central - PubMed

Affiliation: Section of Molecular and Cellular Biology, University of California Davis, Davis, California 95616, USA.

ABSTRACT
Mutations in the dynamin-related GTPase, Mgm1p, have been shown to cause mitochondrial aggregation and mitochondrial DNA loss in Saccharomyces cerevisiae cells, but Mgm1p's exact role in mitochondrial maintenance is unclear. To study the primary function of MGM1, we characterized new temperature sensitive MGM1 alleles. Examination of mitochondrial morphology in mgm1 cells indicates that fragmentation of mitochondrial reticuli is the primary phenotype associated with loss of MGM1 function, with secondary aggregation of mitochondrial fragments. This mgm1 phenotype is identical to that observed in cells with a conditional mutation in FZO1, which encodes a transmembrane GTPase required for mitochondrial fusion, raising the possibility that Mgm1p is also required for fusion. Consistent with this idea, mitochondrial fusion is blocked in mgm1 cells during mating, and deletion of DNM1, which encodes a dynamin-related GTPase required for mitochondrial fission, blocks mitochondrial fragmentation in mgm1 cells. However, in contrast to fzo1 cells, deletion of DNM1 in mgm1 cells restores mitochondrial fusion during mating. This last observation indicates that despite the phenotypic similarities observed between mgm1 and fzo1 cells, MGM1 does not play a direct role in mitochondrial fusion. Although Mgm1p was recently reported to localize to the mitochondrial outer membrane, our studies indicate that Mgm1p is localized to the mitochondrial intermembrane space. Based on our localization data and Mgm1p's structural homology to dynamin, we postulate that it functions in inner membrane remodeling events. In this context, the observed mgm1 phenotypes suggest that inner and outer membrane fission is coupled and that loss of MGM1 function may stimulate Dnm1p-dependent outer membrane fission, resulting in the formation of mitochondrial fragments that are structurally incompetent for fusion.

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Models for Mgm1p function in mitochondrial inner membrane remodeling events. Mgm1p oligomeric ring structures are depicted in red. Mgm1p may help form and/or stabilize inner membrane cristae (A and B) or regulate inner membrane fission (B). See Discussion for details.
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Figure 8: Models for Mgm1p function in mitochondrial inner membrane remodeling events. Mgm1p oligomeric ring structures are depicted in red. Mgm1p may help form and/or stabilize inner membrane cristae (A and B) or regulate inner membrane fission (B). See Discussion for details.

Mentions: This Mgm1p-mediated pinching activity could affect inner membrane structure in several ways. First, Mgm1p might function in the formation or stabilization of inner membrane cristae by self-assembling into ring-like structures around the inner membrane (Fig. 8A and Fig. B). A second possibility is that Mgm1p facilitates inner membrane fission, similar to dynamin and Dnm1p (Fig. 8 B). Finally, a third possibility is that Mgm1p is required sequentially for cristae formation and inner membrane fission as depicted in Fig. 8 B.


The dynamin-related GTPase, Mgm1p, is an intermembrane space protein required for maintenance of fusion competent mitochondria.

Wong ED, Wagner JA, Gorsich SW, McCaffery JM, Shaw JM, Nunnari J - J. Cell Biol. (2000)

Models for Mgm1p function in mitochondrial inner membrane remodeling events. Mgm1p oligomeric ring structures are depicted in red. Mgm1p may help form and/or stabilize inner membrane cristae (A and B) or regulate inner membrane fission (B). See Discussion for details.
© Copyright Policy
Related In: Results  -  Collection

Show All Figures
getmorefigures.php?uid=PMC2192650&req=5

Figure 8: Models for Mgm1p function in mitochondrial inner membrane remodeling events. Mgm1p oligomeric ring structures are depicted in red. Mgm1p may help form and/or stabilize inner membrane cristae (A and B) or regulate inner membrane fission (B). See Discussion for details.
Mentions: This Mgm1p-mediated pinching activity could affect inner membrane structure in several ways. First, Mgm1p might function in the formation or stabilization of inner membrane cristae by self-assembling into ring-like structures around the inner membrane (Fig. 8A and Fig. B). A second possibility is that Mgm1p facilitates inner membrane fission, similar to dynamin and Dnm1p (Fig. 8 B). Finally, a third possibility is that Mgm1p is required sequentially for cristae formation and inner membrane fission as depicted in Fig. 8 B.

Bottom Line: To study the primary function of MGM1, we characterized new temperature sensitive MGM1 alleles.Although Mgm1p was recently reported to localize to the mitochondrial outer membrane, our studies indicate that Mgm1p is localized to the mitochondrial intermembrane space.Based on our localization data and Mgm1p's structural homology to dynamin, we postulate that it functions in inner membrane remodeling events.

View Article: PubMed Central - PubMed

Affiliation: Section of Molecular and Cellular Biology, University of California Davis, Davis, California 95616, USA.

ABSTRACT
Mutations in the dynamin-related GTPase, Mgm1p, have been shown to cause mitochondrial aggregation and mitochondrial DNA loss in Saccharomyces cerevisiae cells, but Mgm1p's exact role in mitochondrial maintenance is unclear. To study the primary function of MGM1, we characterized new temperature sensitive MGM1 alleles. Examination of mitochondrial morphology in mgm1 cells indicates that fragmentation of mitochondrial reticuli is the primary phenotype associated with loss of MGM1 function, with secondary aggregation of mitochondrial fragments. This mgm1 phenotype is identical to that observed in cells with a conditional mutation in FZO1, which encodes a transmembrane GTPase required for mitochondrial fusion, raising the possibility that Mgm1p is also required for fusion. Consistent with this idea, mitochondrial fusion is blocked in mgm1 cells during mating, and deletion of DNM1, which encodes a dynamin-related GTPase required for mitochondrial fission, blocks mitochondrial fragmentation in mgm1 cells. However, in contrast to fzo1 cells, deletion of DNM1 in mgm1 cells restores mitochondrial fusion during mating. This last observation indicates that despite the phenotypic similarities observed between mgm1 and fzo1 cells, MGM1 does not play a direct role in mitochondrial fusion. Although Mgm1p was recently reported to localize to the mitochondrial outer membrane, our studies indicate that Mgm1p is localized to the mitochondrial intermembrane space. Based on our localization data and Mgm1p's structural homology to dynamin, we postulate that it functions in inner membrane remodeling events. In this context, the observed mgm1 phenotypes suggest that inner and outer membrane fission is coupled and that loss of MGM1 function may stimulate Dnm1p-dependent outer membrane fission, resulting in the formation of mitochondrial fragments that are structurally incompetent for fusion.

Show MeSH
Related in: MedlinePlus