Kinesin 13

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Kinesin-13 is a member of the kinesin superfamily of motor proteins that play a critical role in the regulation of microtubule dynamics. Unlike most kinesin proteins that move along microtubules, kinesin-13 members do not function as motor proteins but are involved in microtubule depolymerization. This unique activity is essential for various cellular processes, including mitosis, meiosis, and cytokinesis, making kinesin-13 a key player in cell division.

Function[edit | edit source]

Kinesin-13 proteins bind to the ends of microtubules where they catalyze the removal of tubulin subunits, leading to microtubule depolymerization. This activity is crucial for the proper regulation of microtubule length and dynamics, which is necessary for the accurate segregation of chromosomes during cell division. By controlling microtubule dynamics, kinesin-13 proteins also contribute to the spatial organization of the mitotic spindle, a structure composed of microtubules and associated proteins that segregates chromosomes into the daughter cells during mitosis.

Mechanism[edit | edit source]

The mechanism of action of kinesin-13 involves the recognition of the microtubule end and the induction of curvature in the tubulin dimer structure. This curvature destabilizes the microtubule lattice, promoting the disassembly of tubulin subunits from the microtubule end. Kinesin-13 proteins have a unique motor domain that binds ATP and microtubules, but unlike other kinesins, they do not use ATP hydrolysis to "walk" along microtubules. Instead, ATP hydrolysis is coupled to the conformational changes necessary for microtubule depolymerization.

Clinical Significance[edit | edit source]

Given their role in cell division, kinesin-13 proteins are of significant interest in cancer research. Abnormal expression or function of kinesin-13 members can lead to improper cell division, which is a hallmark of cancer. Therefore, kinesin-13 is being studied as a potential target for cancer therapy, with the aim of developing drugs that can inhibit its activity and thus prevent the proliferation of cancer cells.

Members[edit | edit source]

Several kinesin-13 family members have been identified, including:

  • KIF2A, which is involved in the regulation of microtubule dynamics in neurons and plays a role in neuronal migration and axonal growth.
  • KIF2B, which is expressed during mitosis and is involved in the formation and function of the mitotic spindle.
  • KIF2C, also known as MCAK (Mitotic Centromere-Associated Kinesin), which is a key regulator of microtubule dynamics during mitosis.

Research Directions[edit | edit source]

Research on kinesin-13 continues to uncover its complex roles in cell biology and its potential as a therapeutic target. Future studies are aimed at understanding the precise molecular mechanisms by which kinesin-13 regulates microtubule dynamics, as well as exploring the therapeutic potential of modulating kinesin-13 activity in cancer and other diseases associated with cell division abnormalities.

Kinesin 13
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Contributors: Prab R. Tumpati, MD