Mitochondrial fission factor
Mitochondrial Fission Factor (MFF) is a protein that plays a crucial role in the process of mitochondrial fission, a type of cellular division specific to mitochondria. Mitochondrial fission is essential for cell growth, mitochondrial DNA replication, and distribution of mitochondria during cell division. MFF is involved in recruiting the dynamin-related protein 1 (Drp1) to the outer mitochondrial membrane, where Drp1 facilitates the division of mitochondria.
Function[edit | edit source]
The primary function of MFF is to regulate mitochondrial fission. It acts as a receptor on the mitochondrial surface for Drp1, a GTPase that constricts and divides the mitochondria. By recruiting Drp1 to the mitochondrial outer membrane, MFF ensures the proper distribution of mitochondria into daughter cells during cell division and plays a role in mitochondrial quality control, facilitating the removal of damaged mitochondria via mitophagy.
Structure[edit | edit source]
MFF is a transmembrane protein located on the outer mitochondrial membrane. Its structure allows it to interact with other proteins involved in mitochondrial dynamics, including Drp1 and other fission and fusion mediators. The specific domains of MFF that are critical for its interaction with Drp1 and its role in fission are subjects of ongoing research.
Genetics[edit | edit source]
The gene encoding MFF is located on human chromosome 2. Mutations in this gene can affect mitochondrial fission, leading to various mitochondrial diseases and disorders. Research into the genetic regulation of MFF and its interactions with other proteins involved in mitochondrial dynamics is crucial for understanding and potentially treating these conditions.
Clinical Significance[edit | edit source]
Alterations in mitochondrial fission and fusion are associated with a range of human diseases, including neurodegenerative diseases, cardiovascular diseases, and metabolic syndrome. Given its role in mitochondrial fission, MFF is a potential target for therapeutic interventions aimed at restoring normal mitochondrial function in these diseases. Additionally, understanding the regulation of MFF could lead to insights into the mechanisms of apoptosis (programmed cell death), as mitochondrial fission is a precursor to the apoptotic process.
Research Directions[edit | edit source]
Current research on MFF focuses on elucidating its precise role in mitochondrial fission, its regulation by post-translational modifications, and its interaction with other proteins involved in mitochondrial dynamics. Studies are also exploring the potential of targeting MFF to treat diseases associated with mitochondrial dysfunction.
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Contributors: Prab R. Tumpati, MD