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Meiosis I03:09

Meiosis I

Meiosis is the division of a diploid cell into haploid cells forming sperm and eggs in animals through differentiation. Meiosis I is the first stage of meiosis, where the genetic recombination of homologous chromosomes and the reduction of the ploidy level by half occurs.
Prophase I is the most extended and complex step of meiosis I characterized by synapsis, chromosome pairing, and recombination of the homologous chromosomes. This process is facilitated by a proteinaceous structure called the...
Meiosis II02:02

Meiosis II

Meiosis II entails cell division and segregation of the sister chromatids, resulting in the production of four unique haploid gametes. The steps for meiosis II are similar to mitosis, except that meiosis II occurs in haploid cells, whereas mitosis occurs in diploid cells.
The timing and cell division patterns of meiosis differ between males and females. In male meiosis, the centrosomes are part of the formation of the meiotic spindle. However, in oocytes, including that of humans, Drosophila,...
Meiosis II01:57

Meiosis II

Meiosis II is the second and final stage of meiosis. It relies on the haploid cells produced during meiosis I, each of which contain only 23 chromosomes—one from each homologous initial pair. Importantly, each chromosome in these cells is composed of two joined copies, and when these cells enter meiosis II, the goal is to separate such sister chromatids using the same microtubule-based network employed in other division processes. The result of meiosis II is two haploid cells, each containing...
Meiosis vs. Mitosis02:57

Meiosis vs. Mitosis

Cell division is necessary for growth and reproduction in organisms. Mitosis aids cell growth and development by dividing somatic cells. In contrast, meiosis causes the division of germ cells and plays an essential role in sexual reproduction. Due to their unique functional requirements, mitosis and meiosis differ from each other in multiple aspects.
Before the start of mitosis and meiosis I, the cell synthesizes DNA, resulting in two homologous copies of each chromosome. DNA synthesis is...
Karyotyping01:17

Karyotyping

Describing the number and physical features of chromosomes can reveal abnormalities that underlie genetic diseases. This description is facilitated by special staining techniques that produce a particular banding pattern on each chromosome. State-of-the-art techniques make this approach even more powerful, enabling the detection of individual genes that cause disease.A Simple Chromosome Staining Technique Provides Valuable Scientific InsightSome genetic diseases can be detected by looking at...

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Strand-Specific RNA-Seq Analyses of Fruiting Body Development in Coprinopsis cinerea.

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Simultaneous sequencing of oxidized methylcytosines produced by TET/JBP dioxygenases in Coprinopsis cinerea.

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Lineage-specific expansions of TET/JBP genes and a new class of DNA transposons shape fungal genomic and epigenetic landscapes.

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Related Experiment Video

Updated: Jun 20, 2026

Manipulation of Ploidy in Caenorhabditis elegans
07:54

Manipulation of Ploidy in Caenorhabditis elegans

Published on: March 15, 2018

Meiotic cytogenetics in Coprinus cinereus.

Miriam E Zolan1, Patricia J Pukkila

  • 1Department of Biology, Indiana University, Bloomington, IN, USA.

Methods in Molecular Biology (Clifton, N.J.)
|August 18, 2009
PubMed
Summary

This study details two common methods for analyzing meiosis in the fungus Coprinus cinereus: staining gill segments and chromosome spreads. These techniques aid in studying meiotic progression and chromosome pairing in this model organism.

Area of Science:

  • Mycology
  • Cell Biology
  • Genetics

Background:

  • Coprinus cinereus, a basidiomycete fungus, exhibits naturally synchronous meiosis.
  • It is a well-established model organism with advanced genetic and molecular tools available for research.

Purpose of the Study:

  • To provide detailed explanations of two primary methods for analyzing meiosis in Coprinus cinereus.
  • To illustrate the application of these techniques in studying meiotic progression and chromosome pairing.

Main Methods:

  • Iron-hematoxylin staining of intact gill segments for brightfield microscopy of meiotic progression.
  • Surface spreads combined with fluorescence in situ hybridization (FISH) for investigating meiotic chromosome pairing.
  • Alternative staining of gill segments with DAPI for meiotic stage determination or propidium iodide for DNA content quantitation.

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Preparation of Meiotic Chromosome Spreads from Mouse Oocytes for Assessment of Synapsis and Recombination
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Preparation of Meiotic Chromosome Spreads from Mouse Oocytes for Assessment of Synapsis and Recombination

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Mouse Oocyte Microinjection, Maturation and Ploidy Assessment
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Mouse Oocyte Microinjection, Maturation and Ploidy Assessment

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Last Updated: Jun 20, 2026

Manipulation of Ploidy in Caenorhabditis elegans
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Manipulation of Ploidy in Caenorhabditis elegans

Published on: March 15, 2018

Preparation of Meiotic Chromosome Spreads from Mouse Oocytes for Assessment of Synapsis and Recombination
09:24

Preparation of Meiotic Chromosome Spreads from Mouse Oocytes for Assessment of Synapsis and Recombination

Published on: July 18, 2025

Mouse Oocyte Microinjection, Maturation and Ploidy Assessment
07:03

Mouse Oocyte Microinjection, Maturation and Ploidy Assessment

Published on: July 23, 2011

Main Results:

  • Detailed protocols for iron-hematoxylin staining and chromosome spreads are presented.
  • Demonstration of how these methods can be applied to study meiotic events in C. cinereus.
  • The described chromosome spreading techniques are also suitable for immunolocalization of chromosomal proteins.

Conclusions:

  • The described staining and chromosome spread methods are effective for detailed analysis of meiosis in Coprinus cinereus.
  • These techniques facilitate the study of meiotic progression, chromosome pairing, DNA content, and chromosomal protein localization.
  • Coprinus cinereus remains a valuable model for advancing our understanding of meiosis.