Target type: biologicalprocess
Any process that activates or increases the frequency, rate or extent of microtubule depolymerization. [GOC:mah]
Positive regulation of microtubule depolymerization is a crucial biological process that controls the dynamic disassembly of microtubules, which are essential cytoskeletal structures involved in various cellular functions, including cell division, intracellular transport, and cell migration. Microtubules are composed of α- and β-tubulin dimers that assemble into protofilaments, which then associate laterally to form hollow cylinders. The dynamic instability of microtubules allows for rapid growth and shrinkage, enabling them to explore the cellular environment and perform their diverse roles.
Microtubule depolymerization is regulated by a complex network of proteins, including microtubule-severing proteins, depolymerases, and microtubule-associated proteins (MAPs).
**Microtubule-severing proteins** act by breaking microtubules into shorter fragments, thereby increasing the number of free ends available for depolymerization. Examples include katanin and spastin.
**Depolymerases** directly bind to microtubule ends and promote the release of tubulin dimers, leading to depolymerization. One prominent example is stathmin.
**MAPs** can also play a regulatory role by interacting with microtubules and influencing their stability. Some MAPs promote microtubule polymerization, while others promote depolymerization.
The process of positive regulation of microtubule depolymerization is often triggered by external stimuli, such as stress signals or developmental cues. These signals can activate signaling pathways that lead to the recruitment and activation of depolymerizing factors. For instance, during mitosis, the phosphorylation of stathmin by cyclin-dependent kinase 1 (CDK1) promotes its activity and accelerates microtubule depolymerization, facilitating chromosome segregation.
The dynamic regulation of microtubule depolymerization is essential for maintaining microtubule homeostasis and ensuring proper cellular function. Dysregulation of this process can lead to various cellular pathologies, including defects in cell division, impaired intracellular transport, and neurodegenerative diseases.
In summary, positive regulation of microtubule depolymerization is a complex process involving multiple protein players that act in concert to control the dynamic disassembly of microtubules. This process is crucial for maintaining cellular integrity and function and is tightly regulated in response to various cellular cues.'
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Protein | Definition | Taxonomy |
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Transient receptor potential cation channel subfamily V member 4 | A transient receptor potential cation channel TRPV4 that is encoded in the genome of human. [PRO:CNA, UniProtKB:Q9HBA0] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
cannabinol | Cannabinol: A physiologically inactive constituent of Cannabis sativa L. | dibenzopyran | |
cannabichromene | 1-benzopyran | ||
(6ar-trans)-isomer of tetrahydrocannabivarin 9 | |||
hc 030031 | 2-(1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-7H-purin-7-yl)-N-(4-isopropylphenyl)acetamide: a TRPA1 channel blocker | ||
hc-067047 | HC-067047: a TRPA1 antagonist; structure in first source | ||
rn 1734 | RN 1734: a TRPV4 antagonist; structure in first source | ||
cannabigerol | cannabigerol : A member of the class of resorcinols that is resorcinol which is substituted by a (2E)-3,7-dimethylocta-2,6-dien-1-yl group at position 2 and by a pentyl group at position 5. It is a natural product found in Cannabis sativa and Helichrysum species. cannabigerol: RN given refers to (E)-isomer; structure given in first source | phytocannabinoid; resorcinols | anti-inflammatory agent; antibacterial agent; antioxidant; appetite enhancer; cannabinoid receptor agonist; neuroprotective agent; plant metabolite |
cannabidivarin | cannabidivarin: from Cannabis sativa | monoterpenoid | |
gsk 1016790a | GSK1016790A : A tertiary carboxamide that is piperazine in which one of the amino groups has undergone condensation with the carboxy group of N-[(2,4-dichlorophenyl)sulfonyl]-L-serine, while the other has undergone condensation with the carboxy group of N-(1-benzothiophen-2-ylcarbonyl)-L-leucine. It is a cell-permeable, potent and selective agonist of the TRPV4 (transient receptor potential vanilloid 4) channel. | 1-benzothiophenes; aromatic primary alcohol; dichlorobenzene; N-acylpiperazine; sulfonamide; tertiary carboxamide | TRPV4 agonist |