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Mitosis and Cytokinesis

Mitosis and Cytokinesis

In eukaryotes, the cell division cycle is divided into distinct, coordinated cellular processes that include cell growth, DNA replication/chromosome duplication, chromosome distribution to daughter cells, and finally, cell division. The cell cycle is tightly regulated by its regulatory systems as well as extracellular signals that affect cell proliferation.
The processes of the cell cycle occur over approximately 24 hours (in typical human cells) and in two major distinguishable stages. The...

Mitosis and Cytokinesis

Mitosis and Cytokinesis

In eukaryotes, the cell division cycle is divided into distinct, coordinated cellular processes that include cell growth, DNA replication/chromosome duplication, chromosome distribution to daughter cells, and finally, cell division. The cell cycle is tightly regulated by its regulatory systems as well as extracellular signals that affect cell proliferation.
The processes of the cell cycle occur over approximately 24 hours (in typical human cells) and in two major distinguishable stages. The...

Mitosis and Cytokinesis

Mitosis and Cytokinesis

In eukaryotes, the cell division cycle is divided into distinct, coordinated cellular processes that include cell growth, DNA replication/chromosome duplication, chromosome distribution to daughter cells, and finally, cell division. The cell cycle is tightly regulated by its regulatory systems as well as extracellular signals that affect cell proliferation.
The processes of the cell cycle occur over approximately 24 hours (in typical human cells) and in two major distinguishable stages. The...

Mitosis And Cytokinesis

Mitosis And Cytokinesis

In eukaryotes, the cell division cycle is divided into distinct, coordinated cellular processes that include cell growth, DNA replication/chromosome duplication, chromosome distribution to daughter cells, and finally, cell division. The cell cycle is tightly regulated by its regulatory systems as well as extracellular signals that affect cell proliferation.
The processes of the cell cycle occur over approximately 24 hours (in typical human cells) and in two major distinguishable stages. The...

Crossing Over

Crossing Over

Unlike mitosis, meiosis aims for genetic diversity in its creation of haploid gametes. Dividing germ cells first begin this process in prophase I, where each chromosome—replicated in S phase—is now composed of two sister chromatids (identical copies) joined centrally.
The homologous pairs of sister chromosomes—one from the maternal and one from the paternal genome—then begin to align alongside each other lengthwise, matching corresponding DNA positions in a process called synapsis.
In order to...

Crossing Over

Crossing Over

Crossing over is the exchange of genetic information between homologous chromosomes during prophase I of meiosis I. Genetic recombination gives rise to allelic diversity in the newly formed daughter cells. In humans, crossing over produces genetically distinct haploid egg and sperm cells that undergo fertilization to produce unique offspring. Before cell division starts, the germ cell’s chromosome(s) undergo duplication in the S phase of the cell cycle. As the cells enter prophase I, duplicated...

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Related Experiment Video

Updated: May 12, 2026

A Cell Free Assay to Study Chromatin Decondensation at the End of Mitosis

A Cell Free Assay to Study Chromatin Decondensation at the End of Mitosis

Published on: December 19, 2015

Chromatin reorganization through mitosis.

Paola Vagnarelli¹

¹Heinz Wolff Building, Brunel University, Uxbridge, United Kingdom. Paola.Vagnarelli@brunel.ac.uk

Advances in Protein Chemistry and Structural Biology

|April 16, 2013

Summary

Mitotic chromosome condensation is crucial for accurate genome transmission. This chapter explores the molecular mechanisms and specialized structures like centromeres involved in this process, ensuring cell identity is maintained.

Area of Science:

Molecular Biology
Cell Biology
Genetics

Background:

Chromosome condensation is a key event in cell division, essential for genome stability.
Understanding the molecular mechanisms of chromatin compaction during mitosis remains a challenge.

Purpose of the Study:

To analyze the current understanding of chromatin condensation during mitosis.
To identify key molecular players involved in triggering and maintaining mitotic chromosome conformation.
To discuss the structure and function of specific chromatin domains, such as centromeres.
To explore mechanisms ensuring cell identity transmission despite transcriptional silencing during mitosis.

Main Methods:

Literature review and analysis of current research on chromosome condensation.

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Chromatin Spread Preparations for the Analysis of Mouse Oocyte Progression from Prophase to Metaphase II

Chromatin Spread Preparations for the Analysis of Mouse Oocyte Progression from Prophase to Metaphase II

Published on: February 26, 2018

Live Cell Imaging to Assess the Dynamics of Metaphase Timing and Cell Fate Following Mitotic Spindle Perturbations

Live Cell Imaging to Assess the Dynamics of Metaphase Timing and Cell Fate Following Mitotic Spindle Perturbations

Published on: September 20, 2019

Related Experiment Videos

Last Updated: May 12, 2026

A Cell Free Assay to Study Chromatin Decondensation at the End of Mitosis

A Cell Free Assay to Study Chromatin Decondensation at the End of Mitosis

Published on: December 19, 2015

Chromatin Spread Preparations for the Analysis of Mouse Oocyte Progression from Prophase to Metaphase II

Chromatin Spread Preparations for the Analysis of Mouse Oocyte Progression from Prophase to Metaphase II

Published on: February 26, 2018

Live Cell Imaging to Assess the Dynamics of Metaphase Timing and Cell Fate Following Mitotic Spindle Perturbations

Live Cell Imaging to Assess the Dynamics of Metaphase Timing and Cell Fate Following Mitotic Spindle Perturbations

Published on: September 20, 2019

Examination of molecular players and their roles in chromatin remodeling.

Discussion of specialized chromatin domains (e.g., centromeres).

Main Results:

Detailed analysis of molecular players driving mitotic chromosome condensation.
Exploration of the unique structure and function of centromeres within condensed chromosomes.
Presentation of mechanisms that preserve cell lineage identity across cell division.

Conclusions:

Significant progress has been made in understanding mitotic chromosome condensation, yet molecular details are still emerging.
Specialized chromatin structures like centromeres play critical roles.
Cells possess robust mechanisms to maintain transcriptional memory and cell identity through mitosis.