Mitochondrial fusion

Last updated September 03, 2024

Mitochondria are dynamic organelles with the ability to fuse and divide (fission), forming constantly changing tubular networks in most eukaryotic cells. These mitochondrial dynamics, first observed over a hundred years ago^[1] are important for the health of the cell, and defects in dynamics lead to genetic disorders. Through fusion, mitochondria can overcome the dangerous consequences of genetic malfunction.^[2] The process of mitochondrial fusion involves a variety of proteins that assist the cell throughout the series of events that form this process.

Process overview

When cells experience metabolic or environmental stresses, mitochondrial fusion and fission work to maintain functional mitochondria. An increase in fusion activity leads to mitochondrial elongation, whereas an increase in fission activity results in mitochondrial fragmentation.^[3] The components of this process can influence programmed cell death and lead to neurodegenerative disorders such as Parkinson's disease. Such cell death can be caused by disruptions in the process of either fusion or fission.^[4]

The shapes of mitochondria in cells are continually changing via a combination of fission, fusion, and motility. Specifically, fusion assists in modifying stress by integrating the contents of slightly damaged mitochondria as a form of complementation. By enabling genetic complementation, fusion of the mitochondria allows for two mitochondrial genomes with different defects within the same organelle to individually encode what the other lacks. In doing so, these mitochondrial genomes generate all of the necessary components for a functional mitochondrion.^[2]

With mitochondrial fission

The combined effects of continuous fusion and fission give rise to mitochondrial networks. The mechanisms of mitochondrial fusion and fission are regulated by proteolysis and posttranslational modifications. The actions of fission, fusion and motility cause the shapes of mitochondria to continually change.

The changes in balance between the rates of mitochondrial fission and fusion directly affect the wide range of mitochondrial lengths that can be observed in different cell types. Rapid fission and fusion of the mitochondria in cultured fibroblasts has been shown to promote the redistribution of mitochondrial green fluorescent protein (GFP) from one mitochondrion to all of the other mitochondria. This process can occur in a cell within a time period as short as an hour.^[4]

The significance of mitochondrial fission and fusion is distinct for nonproliferating neurons, which are unable to survive without mitochondrial fission. Such nonproliferating neurons cause two human diseases known as dominant optic atrophy and Charcot Marie Tooth disease type 2A, which are both caused by fusion defects. Though the importance of these processes is evident, it is still unclear why mitochondrial fission and fusion are necessary for nonproliferating cells.

Regulation

Many gene products that control mitochondrial fusion have been identified, and can be reduced to three core groups which also control mitochondrial fission. These groups of proteins include mitofusins, OPA1/Mgm1, and Drp1/Dnm1. All of these molecules are GTP hydrolyzing proteins (GTPases) that belong to the dynamin family. Mitochondrial dynamics in different cells are understood by the way in which these proteins regulate and bind to each other.^[2] These GTPases in control of mitochondrial fusion are well conserved between mammals, flies, and yeast. Mitochondrial fusion mediators differ between the outer and inner membranes of the mitochondria. Specific membrane-anchored dynamin family members mediate fusion between mitochondrial outer membranes known as Mfn1 and Mfn2. These two proteins are mitofusin contained within humans that can alter the morphology of affected mitochondria in over-expressed conditions. However, a single dynamin family member known as OPA1 in mammals mediates fusion between mitochondrial inner membranes. These regulating proteins of mitochondrial fusion are organism-dependent; therefore, in Drosophila (fruit flies) and yeasts, the process is controlled by the mitochondrial transmembrane GTPase, Fzo. In Drosophila, Fzo is found in postmeiotic spermatids and the dysfunction of this protein results in male sterility. However, a deletion of Fzo1 in budding yeast results in smaller, spherical mitochondria due to the lack of mitochondrial DNA (mtDNA).

Apoptosis

The balance between mitochondrial fusion and fission in cells is dictated by the up-and-down regulation of mitofusins, OPA1/Mgm1, and Drp1/Dnm1. Apoptosis, or programmed cell death, begins with the breakdown of mitochondria into smaller pieces. This process results from up-regulation of Drp1/Dnm1 and down-regulation of mitofusins. Later in the apoptosis cycle, an alteration of OPA1/Mgm1 activity within the inner mitochondrial membrane occurs. The role of the OPA1 protein is to protect cells against apoptosis by inhibiting the release of cytochrome c. Once this protein is altered, there is a change in the cristae structure, release of cytochrome c, and the activation of the destructive caspase enzymes. These resulting changes indicate that inner mitochondrial membrane structure is linked with regulatory pathways in influencing cell life and death. OPA1 plays both a genetic and molecular role in mitochondrial fusion and in cristae remodeling during apoptosis.^[5] OPA1 exists in two forms; the first being soluble and found in the intermembrane space, and the second as an integral inner membrane form, work together to restructure and shape the cristae during and after apoptosis. OPA1 blocks intramitochondrial cytochrome c redistribution which proceeds remodeling of the cristae. OPA1 functions to protect cells with mitochondrial dysfunction due to Mfn deficiencies, doubly for those lacking Mfn1 and Mfn2, but it plays a greater role in cells with only Mfn1 deficiencies as opposed to Mfn2 deficiencies. Therefore, it is supported that OPA1 function is dependent on the amount of Mfn1 present in the cell to promote mitochondrial elongation.^[6]

In mammals

Both proteins, Mfn1 and Mfn2, can act either together or separately during mitochondrial fusion. Mfn1 and Mfn2 are 81% similar to each other and about 51% similar to the Drosophila protein Fzo. Results published for a study to determine the impact of fusion on mitochondrial structure revealed that Mfn-deficient cells demonstrated either elongated cells (majority) or small, spherical cells upon observation.

The Mfn protein has three different methods of action: Mfn1 homotypic oligomers, Mfn2 homotypic oligomers and Mfn1-Mfn2 heterotypic oligomers. It has been suggested that the type of cell determines the method of action but it has yet to be concluded whether or not Mfn1 and Mfn2 perform the same function in the process or if they are separate. Cells lacking this protein are subject to severe cellular defects such as poor cell growth, heterogeneity of mitochondrial membrane potential and decreased cellular respiration.^[7]

Mitochondrial fusion plays an important role in the process of embryonic development, as shown through the Mfn1 and Mfn2 proteins. Using Mfn1 and Mfn2 knock-out mice, which die in utero at midgestation due to a placental deficiency, mitochondrial fusion was shown not to be essential for cell survival in vitro, but necessary for embryonic development and cell survival throughout later stages of development. Mfn1 Mfn2 double knock-out mice, which die even earlier in development, were distinguished from the "single" knock-out mice. Mouse embryo fibroblasts (MEFs) originated from the double knock-out mice, which do survive in culture even though there is a complete absence of fusion, but parts of their mitochondria show a reduced mitochondrial DNA (mtDNA) copy number and lose membrane potential. This series of events causes problems with adenosine triphosphate (ATP) synthesis.

The Mitochondrial Inner/Outer Membrane Fusion (MMF) Family

The Mitochondrial Inner/Outer Membrane Fusion (MMF) Family (TC# 9.B.25) is a family of proteins that play a role in mitochondrial fusion events. This family belongs to the larger Mitochondrial Carrier (MC) Superfamily. The dynamic nature of mitochondria is critical for function. Chen and Chan (2010) have discussed the molecular basis of mitochondrial fusion, its protective role in neurodegeneration, and its importance in cellular function.^[8] The mammalian mitofusins Mfn1 and Mfn2, GTPases localized to the outer membrane, mediate outer-membrane fusion. OPA1, a GTPase associated with the inner membrane, mediates subsequent inner-membrane fusion. Mutations in Mfn2 or OPA1 cause neurodegenerative diseases. Mitochondrial fusion enables content mixing within a mitochondrial population, thereby preventing permanent loss of essential components. Cells with reduced mitochondrial fusion show a subpopulation of mitochondria that lack mtDNA nucleoids. Such mtDNA defects lead to respiration-deficient mitochondria, and their accumulation in neurons leads to impaired outgrowth of cellular processes and consequent neurodegeneration.

Family members

A representative list of the proteins belonging to the MMF family is available in the Transporter Classification Database.

9.B.25.1.1 - The mitochondrial inner/outer membrane fusion complex, Fzo/Mgm1/Ugo1. Only the Ugo1 protein is a member of the MC superfamily.
9.B.25.2.1 - The mammalian mitochondrial membrane fusion complex, Mitofusin 1 (Mfn1)/Mfn2/Optical Atrophy Protein 1 (OPA1) complex. This subfamily includes mitofusins 1 and 2.

Mitofusins: Mfn1 and Mfn2

Mfn1 and Mfn2 (TC# 9.B.25.2.1; Q8IWA4 and O95140, respectively), in mammalian cells are required for mitochondrial fusion, Mfn1 and Mfn2 possess functional distinctions. For instance, the formation of tethered structures in vitro occurs more readily when mitochondria are isolated from cells overexpressing Mfn1 than Mfn2.^[9] In addition, Mfn2 specifically has been shown to associate with Bax and Bak (Bcl-2 family, TC#1.A.21), resulting in altered Mfn2 activity, indicating that the mitofusins possess unique functional characteristics. Lipidic holes may open on opposing bilayers as intermediates, and fusion in cardiac myocytes is coupled with outer mitochondrial membrane destabilization that is opportunistically employed during the mitochondrial permeability transition.^[10]

Mutations in Mfn2 (but not Mfn1) result in the neurological disorder Charcot-Marie-Tooth syndrome. These mutations can be complemented by the formation of Mfn1–Mfn2^CMT2A hetero-oligomers but not homo-oligomers of Mfn2⁺–Mfn2^CMT2A_.^[11] This suggests that within the Mfn1–Mfn2 hetero-oligomeric complex, each molecule is functionally distinct. This suggests that control of the expression levels of each protein likely represents the most basic form of regulation to alter mitochondrial dynamics in mammalian tissues. Indeed, the expression levels of Mfn1 and Mfn2 vary according to cell or tissue type as does the mitochondrial morphology.^[12]

Yeast mitochondrial fusion proteins

In yeast, three proteins are essential for mitochondrial fusion. Fzo1 (P38297) and Mgm1 (P32266) are conserved guanosine triphosphatases that reside in the outer and inner membranes, respectively. At each membrane, these conserved proteins are required for the distinct steps of membrane tethering and lipid mixing. The third essential component is Ugo1, an outer membrane protein with a region homologous to but distantly related to a region in the Mitochondrial Carrier (MC) family. Hoppins et al., 2009 showed that Ugo1 is a modified member of this family, containing three transmembrane domains and existing as a dimer, a structure that is critical for the fusion function of Ugo1.^[13] Their analyses of Ugo1 indicate that it is required for both outer and inner membrane fusion after membrane tethering, indicating that it operates at the lipid-mixing step of fusion. This role is distinct from the fusion dynamin-related proteins and thus demonstrates that at each membrane, a single fusion protein is not sufficient to drive the lipid-mixing step. Instead, this step requires a more complex assembly of proteins. The formation of a fusion pore has not yet been demonstrated.^[13]^[14] The Ugo1 protein is a member of the MC superfamily.

Related Research Articles

A mitochondrion (pl. mitochondria) is an organelle found in the cells of most eukaryotes, such as animals, plants and fungi. Mitochondria have a double membrane structure and use aerobic respiration to generate adenosine triphosphate (ATP), which is used throughout the cell as a source of chemical energy. They were discovered by Albert von Kölliker in 1857 in the voluntary muscles of insects. Meaning a thread-like granule, the term mitochondrion was coined by Carl Benda in 1898. The mitochondrion is popularly nicknamed the "powerhouse of the cell", a phrase popularized by Philip Siekevitz in a 1957 Scientific American article of the same name.

Dominant optic atrophy (DOA), or autosomal dominant optic atrophy (ADOA), (Kjer's type) is an autosomally inherited disease that affects the optic nerves, causing reduced visual acuity and blindness beginning in childhood. However, the disease can seem to re-present a second time with further vision loss due to the early onset of presbyopia symptoms (i.e., difficulty in viewing objects up close). DOA is characterized as affecting neurons called retinal ganglion cells (RGCs). This condition is due to mitochondrial dysfunction mediating the death of optic nerve fibers. The RGCs axons form the optic nerve. Therefore, the disease can be considered of the central nervous system. Dominant optic atrophy was first described clinically by Batten in 1896 and named Kjer’s optic neuropathy in 1959 after Danish ophthalmologist Poul Kjer, who studied 19 families with the disease. Although dominant optic atrophy is the most common autosomally inherited optic neuropathy (i.e., disease of the optic nerves), it is often misdiagnosed.

Dynamin is a GTPase responsible for endocytosis in the eukaryotic cell. Dynamin is part of the "dynamin superfamily", which includes classical dynamins, dynamin-like proteins, Mx proteins, OPA1, mitofusins, and GBPs. Members of the dynamin family are principally involved in the scission of newly formed vesicles from the membrane of one cellular compartment and their targeting to, and fusion with, another compartment, both at the cell surface as well as at the Golgi apparatus. Dynamin family members also play a role in many processes including division of organelles, cytokinesis and microbial pathogen resistance.

Mitofusin-2 is a protein that in humans is encoded by the MFN2 gene. Mitofusins are GTPases embedded in the outer membrane of the mitochondria. In mammals MFN1 and MFN2 are essential for mitochondrial fusion. In addition to the mitofusins, OPA1 regulates inner mitochondrial membrane fusion, and DRP1 is responsible for mitochondrial fission.

Dynamin-like 120 kDa protein, mitochondrial is a protein that in humans is encoded by the OPA1 gene. This protein regulates mitochondrial fusion and cristae structure in the inner mitochondrial membrane (IMM) and contributes to ATP synthesis and apoptosis, and small, round mitochondria. Mutations in this gene have been implicated in dominant optic atrophy (DOA), leading to loss in vision, hearing, muscle contraction, and related dysfunctions.

Dynamin-1-like protein is a GTPase that regulates mitochondrial fission. In humans, dynamin-1-like protein, which is typically referred to as dynamin-related protein 1 (Drp1), is encoded by the DNM1L gene and is part of the dynamin superfamily (DSP) family of proteins.

Mitochondrial fission 1 protein (FIS1) is a protein that in humans is encoded by the FIS1 gene on chromosome 7. This protein is a component of a mitochondrial complex, the ARCosome, that promotes mitochondrial fission. Its role in mitochondrial fission thus implicates it in the regulation of mitochondrial morphology, the cell cycle, and apoptosis. By extension, the protein is involved in associated diseases, including neurodegenerative diseases and cancers.

Mitofusin-1 is a protein that in humans is encoded by the MFN1 gene.

Mitochondrial Rho GTPase 2 is an enzyme that in humans is encoded by the RHOT2 gene. As a Miro protein isoform, the protein facilitates mitochondrial transport by attaching the mitochondria to the motor/adaptor complex. Through its key role in mitochondrial transport, RHOT2 is involved in mitochondrial homeostasis and apoptosis, as well as Parkinson's disease (PD).

ATP-dependent metalloprotease YME1L1 is an enzyme that in humans is encoded by the YME1L1 gene. YME1L1 belongs to the AAA family of ATPases and mainly functions in the maintenance of mitochondrial morphology. Mutations in this gene would cause infantile-onset mitochondriopathy.

E3 ubiquitin-protein ligase MARCH5, also known as membrane-associated ring finger (C3HC4) 5, is an enzyme that, in humans, is encoded by the MARCH5 gene. It is localized in the mitochondrial outer membrane and has four transmembrane domains.

Mitochondrial biogenesis is the process by which cells increase mitochondrial numbers. It was first described by John Holloszy in the 1960s, when it was discovered that physical endurance training induced higher mitochondrial content levels, leading to greater glucose uptake by muscles. Mitochondrial biogenesis is activated by numerous different signals during times of cellular stress or in response to environmental stimuli, such as aerobic exercise.

Mitochondrial fission is the process where mitochondria divide or segregate into two separate mitochondrial organelles. Mitochondrial fission is counteracted by the process of mitochondrial fusion, whereby two separate mitochondria can fuse together to form a large one. Mitochondrial fusion in turn can result in elongated mitochondrial networks. Both mitochondrial fission and fusion are balanced in the cell, and mutations interfering with either processes are associated with a variety of diseases. Mitochondria can divide by prokaryotic binary fission and since they require mitochondrial DNA for their function, fission is coordinated with DNA replication. Some of the proteins that are involved in mitochondrial fission have been identified and some of them are associated with mitochondrial diseases. Mitochondrial fission has significant implications in stress response and apoptosis.

Mitochondrial fission factor (Mff) is a protein that in humans is encoded by the MFF gene. Its primary role is in controlling the division of mitochondria. Mitochondrial morphology changes by continuous fission in order to create interconnected network of mitochondria. This activity is crucial for normal function of mitochondria. Mff is anchored to the mitochondrial outer membrane through the C-terminal transmembrane domain, extruding the bulk of the N-terminal portion containing two short amino acid repeats in the N-terminal half and a coiled-coil domain just upstream of the transmembrane domain into the cytosol. It has also been shown to regulate peroxisome morphology.

Luca Scorrano is an Italian biologist and professor of Biochemistry at the University of Padua as well as the former Scientific Director of the Veneto Institute of Molecular Medicine in Italy. He is known for his important contributions to the field of mitochondrial dynamics and the interface between mitochondria and the endoplasmic reticulum.

Metalloendopeptidase OMA1, mitochondrial is an enzyme that in humans is encoded by the OMA1 gene. OMA1 is a Zn²⁺-dependent metalloendopeptidase in the inner membrane of mitochondria. The OMA1 acronym was derived from overlapping proteolytic activity with m-AAA protease 1.

The mycotoxin phomoxanthone A, or PXA for short, is a toxic natural product that affects the mitochondria. It is the most toxic and the best studied of the naturally occurring phomoxanthones. PXA has recently been shown to induce rapid, non-canonical mitochondrial fission by causing the mitochondrial matrix to fragment while the outer mitochondrial membrane can remain intact. This process was shown to be independent from the mitochondrial fission and fusion regulators DRP1 and OPA1.

Mitochondrial elongation factor 2 is a protein that in humans is encoded by the MIEF2 gene.

Solute carrier family 25 member 46 is a protein that in humans is encoded by the SLC25A46 gene. This protein is a member of the SLC25 mitochondrial solute carrier family. It is a transmembrane protein located in the mitochondrial outer membrane involved in lipid transfer from the endoplasmic reticulum (ER) to mitochondria. Mutations in this gene result in neuropathy and optic atrophy.

Dynamin Superfamily Protein (DSP) is a protein superfamily includes classical dynamins, GBPs, Mx proteins, OPA1, mitofusins in Eukaryote, and bacterial dynamin-like proteins (BDLPs) in Prokaryote. DSPs mediate eukaryotic membrane fusion and fission necessary for endocytosis, organelle biogenesis and maintenance, Mitochondrial fusion and fission, as well as for prokaryotic cytokinesis.

References

↑ Lewis, Margaret (1915). "Mitochondria (and other cytoplamic structures) in tissue cultures" (PDF). American Journal of Anatomy. 17 (3): 339–401. doi:10.1002/aja.1000170304.
1 2 3 Hales, Karen G. (2010). "Mitochondrial Fusion and Division". Nature Education. 3 (9): 12. Retrieved 23 November 2014.
↑ Chan, DC (2006). "Mitochondrial fusion and fission in mammals" (PDF). Annual Review of Cell and Developmental Biology. 22: 79–99. doi:10.1146/annurev.cellbio.22.010305.104638. PMID 16704336.
1 2 Youle, Richard J. (31 August 2012). "Mitochondrial Fission, Fusion, and Stress". Science Magazine. 337 (6098): 1062–1065. Bibcode:2012Sci...337.1062Y. doi:10.1126/science.1219855. PMC 4762028 . PMID 22936770.
↑ Frezza, C; Cipolat, S; Martins; de Brito, O; Micaroni, M; Benznoussenko, GV; Rudka, T; Bartoli, D; Polishuck, RS; Danial, NN; De Strooper, B; Scorrano, L (2006). "OPA1 controls apoptotic cristae remodeling independently from mitochondrial fusion". Cell. 126 (1): 177–189. doi: 10.1016/j.cell.2006.06.025 . PMID 16839885. S2CID 11569831.
↑ Cipolat, S; Martins; de Brito, O; Dal Zilio, B; Scorrano, L (2004). "OPA1 requires mitofusin 1 to promote mitochondrial fusion". Proceedings of the National Academy of Sciences of the United States of America. 101 (45): 15927–15932. Bibcode:2004PNAS..10115927C. doi: 10.1073/pnas.0407043101 . PMC 528769 . PMID 15509649.
↑ Chen, H; Chomyn, A; Chan, DC (2005). "Disruption of fusion results in mitochondrial heterogeneity and dysfunction". Journal of Biological Chemistry. 280 (28): 26185–26192. doi: 10.1074/jbc.M503062200 . PMID 15899901.
↑ Chen, Hsiuchen; Chan, David C. (2010-07-01). "Physiological functions of mitochondrial fusion". Annals of the New York Academy of Sciences. 1201 (1): 21–25. Bibcode:2010NYASA1201...21C. doi:10.1111/j.1749-6632.2010.05615.x. ISSN 1749-6632. PMID 20649534. S2CID 3072156.
↑ Ishihara, Naotada; Eura, Yuka; Mihara, Katsuyoshi (2004-12-15). "Mitofusin 1 and 2 play distinct roles in mitochondrial fusion reactions via GTPase activity". Journal of Cell Science. 117 (Pt 26): 6535–6546. doi: 10.1242/jcs.01565 . ISSN 0021-9533. PMID 15572413.
↑ Papanicolaou, Kyriakos N.; Phillippo, Matthew M.; Walsh, Kenneth (2012-08-01). "Mitofusins and the mitochondrial permeability transition: the potential downside of mitochondrial fusion". American Journal of Physiology. Heart and Circulatory Physiology. 303 (3): H243–255. doi:10.1152/ajpheart.00185.2012. ISSN 1522-1539. PMC 3423162 . PMID 22636681.
↑ Detmer, Scott A.; Chan, David C. (2007-02-12). "Complementation between mouse Mfn1 and Mfn2 protects mitochondrial fusion defects caused by CMT2A disease mutations". The Journal of Cell Biology. 176 (4): 405–414. doi:10.1083/jcb.200611080. ISSN 0021-9525. PMC 2063976 . PMID 17296794.
↑ Eura, Yuka; Ishihara, Naotada; Yokota, Sadaki; Mihara, Katsuyoshi (2003-09-01). "Two mitofusin proteins, mammalian homologues of FZO, with distinct functions are both required for mitochondrial fusion". Journal of Biochemistry. 134 (3): 333–344. doi:10.1093/jb/mvg150. ISSN 0021-924X. PMID 14561718.
1 2 Hoppins, Suzanne; Nunnari, Jodi (2009-01-01). "The molecular mechanism of mitochondrial fusion". Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1793 (1): 20–26. doi: 10.1016/j.bbamcr.2008.07.005 . ISSN 0006-3002. PMID 18691613.
↑ Hoppins, Suzanne; Horner, Jennifer; Song, Cheng; McCaffery, J. Michael; Nunnari, Jodi (2009-02-23). "Mitochondrial outer and inner membrane fusion requires a modified carrier protein". The Journal of Cell Biology. 184 (4): 569–581. doi:10.1083/jcb.200809099. ISSN 1540-8140. PMC 2654124 . PMID 19237599.

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[Lewis_1915-1] Lewis, Margaret (1915). "Mitochondria (and other cytoplamic structures) in tissue cultures" (PDF). American Journal of Anatomy. 17 (3): 339–401. doi:10.1002/aja.1000170304.

[Hales2010-2] 1 2 3 Hales, Karen G. (2010). "Mitochondrial Fusion and Division". Nature Education. 3 (9): 12. Retrieved 23 November 2014.

[Chan2006-3] Chan, DC (2006). "Mitochondrial fusion and fission in mammals" (PDF). Annual Review of Cell and Developmental Biology. 22: 79–99. doi:10.1146/annurev.cellbio.22.010305.104638. PMID 16704336.

[Youle2012-4] 1 2 Youle, Richard J. (31 August 2012). "Mitochondrial Fission, Fusion, and Stress". Science Magazine. 337 (6098): 1062–1065. Bibcode:2012Sci...337.1062Y. doi:10.1126/science.1219855. PMC 4762028 . PMID 22936770.

[5] Frezza, C; Cipolat, S; Martins; de Brito, O; Micaroni, M; Benznoussenko, GV; Rudka, T; Bartoli, D; Polishuck, RS; Danial, NN; De Strooper, B; Scorrano, L (2006). "OPA1 controls apoptotic cristae remodeling independently from mitochondrial fusion". Cell. 126 (1): 177–189. doi: 10.1016/j.cell.2006.06.025 . PMID 16839885. S2CID 11569831.

[6] Cipolat, S; Martins; de Brito, O; Dal Zilio, B; Scorrano, L (2004). "OPA1 requires mitofusin 1 to promote mitochondrial fusion". Proceedings of the National Academy of Sciences of the United States of America. 101 (45): 15927–15932. Bibcode:2004PNAS..10115927C. doi: 10.1073/pnas.0407043101 . PMC 528769 . PMID 15509649.

[7] Chen, H; Chomyn, A; Chan, DC (2005). "Disruption of fusion results in mitochondrial heterogeneity and dysfunction". Journal of Biological Chemistry. 280 (28): 26185–26192. doi: 10.1074/jbc.M503062200 . PMID 15899901.

[8] Chen, Hsiuchen; Chan, David C. (2010-07-01). "Physiological functions of mitochondrial fusion". Annals of the New York Academy of Sciences. 1201 (1): 21–25. Bibcode:2010NYASA1201...21C. doi:10.1111/j.1749-6632.2010.05615.x. ISSN 1749-6632. PMID 20649534. S2CID 3072156.

[9] Ishihara, Naotada; Eura, Yuka; Mihara, Katsuyoshi (2004-12-15). "Mitofusin 1 and 2 play distinct roles in mitochondrial fusion reactions via GTPase activity". Journal of Cell Science. 117 (Pt 26): 6535–6546. doi: 10.1242/jcs.01565 . ISSN 0021-9533. PMID 15572413.

[10] Papanicolaou, Kyriakos N.; Phillippo, Matthew M.; Walsh, Kenneth (2012-08-01). "Mitofusins and the mitochondrial permeability transition: the potential downside of mitochondrial fusion". American Journal of Physiology. Heart and Circulatory Physiology. 303 (3): H243–255. doi:10.1152/ajpheart.00185.2012. ISSN 1522-1539. PMC 3423162 . PMID 22636681.

[11] Detmer, Scott A.; Chan, David C. (2007-02-12). "Complementation between mouse Mfn1 and Mfn2 protects mitochondrial fusion defects caused by CMT2A disease mutations". The Journal of Cell Biology. 176 (4): 405–414. doi:10.1083/jcb.200611080. ISSN 0021-9525. PMC 2063976 . PMID 17296794.

[12] Eura, Yuka; Ishihara, Naotada; Yokota, Sadaki; Mihara, Katsuyoshi (2003-09-01). "Two mitofusin proteins, mammalian homologues of FZO, with distinct functions are both required for mitochondrial fusion". Journal of Biochemistry. 134 (3): 333–344. doi:10.1093/jb/mvg150. ISSN 0021-924X. PMID 14561718.

[:0-13] 1 2 Hoppins, Suzanne; Nunnari, Jodi (2009-01-01). "The molecular mechanism of mitochondrial fusion". Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1793 (1): 20–26. doi: 10.1016/j.bbamcr.2008.07.005 . ISSN 0006-3002. PMID 18691613.

[14] Hoppins, Suzanne; Horner, Jennifer; Song, Cheng; McCaffery, J. Michael; Nunnari, Jodi (2009-02-23). "Mitochondrial outer and inner membrane fusion requires a modified carrier protein". The Journal of Cell Biology. 184 (4): 569–581. doi:10.1083/jcb.200809099. ISSN 1540-8140. PMC 2654124 . PMID 19237599.

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