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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 ...
Mitochondrial fission is the process by which mitochondria divide or segregate into two separate mitochondrial organelles. Mitochondrial fission is counteracted by mitochondrial fusion, where two mitochondria fuse together to form a larger one. [1] Fusion can result in elongated mitochondrial networks.
In mammals MFN1 and MFN2 are essential for mitochondrial fusion. [7] In addition to the mitofusins, OPA1 regulates inner mitochondrial membrane fusion, and DRP1 is responsible for mitochondrial fission. [8] Mitofusin-2 (MFN2) is a mitochondrial membrane protein that plays a central role in regulating mitochondrial fusion and cell
Fission-fusion society – Social organization; Mitochondrial fusion – Merging of two or more mitochondria within a cell to form a single compartment; Mitosis – Process in which chromosomes are replicated and separated into two new identical nuclei
The processes of fusion and fission allow for mitochondrial reorganization. In mammals, mitochondrial fusion and fission are both controlled by GTPases of the dynamin family. [8] [13] The process of mitochondrial fission is directed by Drp1, a member of the cytosolic dynamin family.
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Mitochondrial dynamics, the balance between mitochondrial fusion and fission, is an important factor in pathologies associated with several disease conditions. [166] The hypothesis of mitochondrial binary fission has relied on the visualization by fluorescence microscopy and conventional transmission electron microscopy (TEM). The resolution of ...
Mff is an outer mitochondrial membrane protein that binds to the GTPase Drp1; the Mff-Drp1 complex is what promotes mitochondrial fission.Knockdown of Mff causes the mitochondrial network to expand (by releasing the Drp1 foci from the outer mitochondrial membrane), while Mff overexpression causes it to become fragmented (by stimulating mitochondrial recruitment of Drp1). [9]