Formins

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Formin proteins.png

Formins are a group of proteins that play a critical role in the formation of actin filaments, one of the key components of the cytoskeleton in eukaryotic cells. Formins are involved in various cellular processes including cell division, cell polarity, and cell migration, making them essential for the proper functioning and development of organisms.

Function[edit | edit source]

Formins nucleate the formation of new actin filaments and remain associated with the growing end, facilitating the elongation process. They are characterized by the presence of the formin homology 2 (FH2) domain, which directly interacts with actin. The FH1 domain, located adjacent to the FH2 domain, binds to profilin-actin complexes, thereby recruiting actin monomers to the site of filament elongation.

In addition to actin assembly, formins are involved in the regulation of microtubule dynamics through interactions with various microtubule-associated proteins. This dual role in regulating both actin and microtubule dynamics positions formins as central coordinators of cytoskeletal remodeling, which is crucial for processes such as mitosis and cell migration.

Classification[edit | edit source]

Formins are classified into several subfamilies based on their domain structure and sequence homology. The most well-known subfamilies include the Diaphanous-related formins (DRFs), which are regulated by Rho GTPases, and the FMN (formin homology proteins in nematodes) subfamily. Each subfamily is associated with distinct cellular functions and regulatory mechanisms.

Regulation[edit | edit source]

The activity of formins is tightly regulated by Rho GTPases, particularly members of the Rho family such as RhoA, Rac1, and Cdc42. These GTPases control the conformational changes in formins that either activate or inhibit their actin-nucleating and -elongating activities. Additionally, formins can be regulated by autoinhibition, a mechanism in which the formin protein adopts a folded conformation that prevents actin interaction, and this inhibition can be relieved through binding to Rho GTPases or other signaling molecules.

Role in Disease[edit | edit source]

Given their pivotal role in cell structure and movement, formins are implicated in a variety of diseases. Aberrations in formin function or expression can lead to disorders of cell migration and polarity, contributing to developmental abnormalities, cancer metastasis, and other pathologies. For example, mutations in the formin gene DIAPH1 have been linked to hearing loss, as proper actin filament assembly in the inner ear is essential for auditory function.

Research and Therapeutic Potential[edit | edit source]

Understanding the mechanisms of formin-mediated actin assembly and its regulation offers potential therapeutic targets for diseases associated with cytoskeletal abnormalities. Small molecule inhibitors that specifically target formin activity are under investigation for their potential to inhibit cancer cell migration and invasion.


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Contributors: Prab R. Tumpati, MD