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View/Edit Mouse. Dynamin-like 120 kDa protein, mitochondrial is a protein that in humans is encoded by the OPA1 gene. [5][6] This protein regulates mitochondrial fusion and cristae structure in the inner mitochondrial membrane (IMM) and contributes to ATP synthesis and apoptosis, [7][8][9] and small, round mitochondria. [10]
More specifically, MFN2 is a dynamin-like GTPase embedded in the outer mitochondrial membrane (OMM) which in turn affects mitochondrial dynamics, distribution, quality control, and function. In addition to the MFN2, OPA1 regulates inner mitochondrial membrane fusion, MFN1 is a mediator of mitochondrial fusion and DRP1 is responsible for ...
Mitochondrial fusion. 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.
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 ...
However, if this molecule can activate or restore parkin function, it could help remove damaged mitochondria even in later stages, potentially slowing disease progression and improving cell health.
Homoplasmy is a term used in genetics to describe a eukaryotic cell whose copies of mitochondrial DNA are all identical. [1] In normal and healthy tissues, all cells are homoplasmic. [2] Homoplasmic mitochondrial DNA copies may be normal or mutated; [1] however, most mutations are heteroplasmic [2][3] (only occurring in some copies of ...
Mitochondrial fission factor. Mitochondrial fission factor (Mff) is a protein that in humans is encoded by the MFF gene. [5] 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 ...
On the other hand, the process of fusion is directed by different membrane-anchored dynamin proteins at different levels of the mitochondria. [13] Fusion at the level of the outer mitochondrial membrane is mediated by Mfn1 and Mfn2 (Mitofusins 1 and 2), [15] and fusion at the level of the inner mitochondrial membrane is mediated by Opa1.