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Related Concept Videos

Spindle Assembly02:50

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...
The Mitotic Spindle02:27

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 Mitotic Spindle02:27

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...
Attachment of Sister Chromatids02:57

Attachment of Sister Chromatids

As cells progress into mitosis, the nuclear envelope breaks down, and the condensed chromosomes are exposed to the array of bipolar microtubules of the mitotic spindle. The kinetochore, a large, disc-shaped protein complex, is present at the centromere region of the sister chromatids and acts as a binding site for the microtubules.  Usually, the plus-end of a single microtubule is embedded within the kinetochore. However, some kinetochores first establish lateral contact with the side-wall of a...
Attachment of Sister Chromatids02:57

Attachment of Sister Chromatids

As cells progress into mitosis, the nuclear envelope breaks down, and the condensed chromosomes are exposed to the array of bipolar microtubules of the mitotic spindle. The kinetochore, a large, disc-shaped protein complex, is present at the centromere region of the sister chromatids and acts as a binding site for the microtubules.  Usually, the plus-end of a single microtubule is embedded within the kinetochore. However, some kinetochores first establish lateral contact with the side-wall of a...
Anaphase A and B01:39

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...

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Related Experiment Video

Updated: Jul 10, 2026

Self-Assembly of Microtubule Tactoids
08:49

Self-Assembly of Microtubule Tactoids

Published on: June 23, 2022

Spindle microtubules: getting attached at both ends.

Jennifer G DeLuca1

  • 1Department of Biochemistry and Molecular Biology, Colorado State University, Fort Collins, Colorado 80523, USA. Jennifer.Deluca@ColoState.edu

Current Biology : CB
|November 22, 2007
PubMed
Summary
This summary is machine-generated.

The centrosomal protein Cep57 plays a new role in connecting spindle microtubules to kinetochores and centrosomes. This suggests that similar attachment mechanisms are used during cell division (mitosis).

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Area of Science:

  • Cell Biology
  • Molecular Biology
  • Genetics

Background:

  • The precise attachment of spindle microtubules is crucial for accurate chromosome segregation during mitosis.
  • Centrosomes act as microtubule organizing centers, initiating spindle formation.
  • Kinetochores are protein structures on chromosomes that serve as attachment sites for spindle microtubules.

Purpose of the Study:

  • To investigate the function of the centrosomal protein Cep57 in microtubule-kinetochore and microtubule-centrosome attachments.
  • To determine if common mechanisms underlie these distinct microtubule linkages during mitosis.

Main Methods:

  • Immunofluorescence microscopy to visualize protein localization and microtubule dynamics.
  • Genetic manipulation to assess the role of Cep57.
  • Biochemical assays to study protein interactions.

Main Results:

  • Cep57 was identified as a key protein involved in linking spindle microtubules to both kinetochores and centrosomes.
  • The study suggests that Cep57 facilitates the formation of these essential mitotic attachments.
  • Evidence points towards conserved molecular mechanisms governing these distinct microtubule interactions.

Conclusions:

  • Cep57 has a novel, dual role in establishing microtubule attachments at both kinetochores and centrosomes.
  • These findings imply shared molecular pathways for generating microtubule linkages critical for accurate mitosis.
  • This research deepens our understanding of the fundamental processes governing cell division.