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Reconstitution of Basic Mitotic Spindles in Spherical Emulsion Droplets
Published on: August 13, 2016
How kinesin motor proteins drive mitotic spindle function: Lessons from molecular assays
1Department of Physiology & Biophysics, University of Washington School of Medicine, Seattle, WA 98195-7290, United States. worde@u.washington.edu
Seminars in Cell & Developmental Biology
|January 30, 2010
Summary
Kinesin motor proteins are essential for cell division. Studying their molecular mechanics helps understand how they function in the mitotic spindle and what causes spindle failure.
Area of Science:
- Biochemistry and Molecular Biology
- Cell Biology
- Biophysics
Background:
- Kinesins are ATP-dependent molecular motors crucial for cellular processes.
- The kinesin superfamily comprises approximately 14 families, classified by motor domain sequence.
- Kinesin function in cell division, particularly chromosome segregation, is vital for fidelity.
Purpose of the Study:
- To review the molecular mechanisms of kinesin motors.
- To correlate single-molecule properties with cellular functions in the mitotic spindle.
- To identify kinesins with incomplete molecular characterization impacting spindle function understanding.
Main Methods:
- Focus on illustrative kinesin families studied at the molecular level.
- Analysis of enzymatic behavior and motility of purified kinesin motors.
- Review of existing literature linking molecular properties to cellular roles.
Main Results:
- Kinesin family classification is based on motor domain sequence alignment.
- Enzymatic activity and motility generally correlate with kinesin family.
- Single-molecule studies are essential for understanding kinesin-driven spindle mechanics.
Conclusions:
- Understanding kinesin molecular properties is key to deciphering their role in spindle function.
- Deficiencies in molecular understanding for some kinesins hinder prediction of their spindle contribution.
- Further molecular studies are needed for a comprehensive grasp of kinesin roles in cell division.
Related Concept Videos
The Mitotic Spindle
The mitotic spindle—or spindle apparatus—is a eukaryotic, cytoskeletal structure made up of long protein fibers called microtubules. Formed during cell division, the spindle separates sister chromatids and moves them to opposite ends of a parental cell, where the now individual chromosomes are distributed to two daughter cell nuclei.
The bipolar configuration of the mitotic spindle facilitates chromosomal segregation, preparing the cell for division. One mechanism that ensures bipolar mitotic...
The bipolar configuration of the mitotic spindle facilitates chromosomal segregation, preparing the cell for division. One mechanism that ensures bipolar mitotic...
The Mitotic Spindle
The mitotic spindle—or spindle apparatus—is a eukaryotic, cytoskeletal structure made up of long protein fibers called microtubules. Formed during cell division, the spindle separates sister chromatids and moves them to opposite ends of a parental cell, where the now individual chromosomes are distributed to two daughter cell nuclei.
The bipolar configuration of the mitotic spindle facilitates chromosomal segregation, preparing the cell for division. One mechanism that ensures bipolar mitotic...
The bipolar configuration of the mitotic spindle facilitates chromosomal segregation, preparing the cell for division. One mechanism that ensures bipolar mitotic...
Spindle Assembly
Spindle assembly occurs through three, often coexisting, pathways – the centrosome-mediated pathway, the chromatin-mediated pathway, and the microtubule-mediated pathway – collectively contributing to form a robust spindle apparatus.
In most cells, centrosomes are the primary microtubule nucleation centers. In the centrosome-mediated pathway, the G2-prophase transition triggers centrosome maturation and increased microtubule nucleation. Progressive nucleation results in a microtubule array...
In most cells, centrosomes are the primary microtubule nucleation centers. In the centrosome-mediated pathway, the G2-prophase transition triggers centrosome maturation and increased microtubule nucleation. Progressive nucleation results in a microtubule array...
Anaphase A and B
Microtubules form through the end-to-end polymerization of tubulin heterodimers. Kinetochore microtubules originate from the spindle poles, and their plus-ends connect with the kinetochores on sister-chromatids. Ndc80 protein complexes, present on the kinetochore, form low-affinity links with the plus end of these kinetochore microtubules.
Plus-end depolymerization releases tubulin heterodimers from the terminal region of the microtubule. As tubulin subunits are lost, the Ndc80 complexes detach...
Plus-end depolymerization releases tubulin heterodimers from the terminal region of the microtubule. As tubulin subunits are lost, the Ndc80 complexes detach...
Microtubule Associated Motor Proteins
Eukaryotic cells have different motor proteins for transporting various cargo within the cell. These motor proteins differ based on the filament they associate with, the direction they move within the cell, and the type of cargo they transport. Motor proteins that associate with microtubules are known as microtubule-associated motor proteins. There are two families of microtubule-associated motor proteins —Kinesins and Dyneins. Both these proteins assist in the transport of cellular cargos...
Forces Acting on Chromosomes
During mitosis, chromosome movements occur through the interplay of multiple piconewton level forces. In prometaphase, these forces help in chromosome assembly or congression at the equatorial plane, eventually leading to their alignment at the metaphase plate. The forces acting on the chromosomes are space and time-dependent; therefore, they vary with the position of the chromosomes as the cell progresses through mitosis.
Microtubules and motor proteins exert two types of forces on...
Microtubules and motor proteins exert two types of forces on...

