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Mitosis Unveiled

Mastering the fundamental process of cell division that drives growth, repair, and asexual reproduction in eukaryotic organisms.

What is Mitosis? ๐Ÿ‘‡ Explore Phases ๐Ÿ”ฌ

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What is Mitosis?

Core Process

Mitosis is a critical part of the cell cycle in eukaryotic cells. It involves the replication and subsequent separation of duplicated chromosomes into two new nuclei. This process ensures that each daughter cell receives an identical set of chromosomes, maintaining genetic stability across cell generations.[1][2]

Cell Cycle Integration

Mitosis is preceded by the S phase of interphase, during which DNA replication occurs. Following mitosis, the cell undergoes telophase and cytokinesis, which divide the cytoplasm, organelles, and cell membrane to form two distinct daughter cells. Together, mitosis and cytokinesis constitute the M phase of the cell cycle, resulting in two genetically identical daughter cells.[2][3]

Mitotic Errors

Errors during mitosis can lead to abnormal cell division, such as tripolar or multipolar mitosis. These errors can result in non-viable embryos, induce programmed cell death (apoptosis), or cause mutations that may contribute to the development of cancers.[7][8]

Historical Discovery

Early Observations

Descriptions of cell division date back to the 18th and 19th centuries. German botanist Hugo von Mohl accurately described cell division in green algae in 1835. In animal cells, mitosis was first identified in frog, rabbit, and cat cornea cells in 1873 by Wacล‚aw Mayzel.[13][18]

Naming the Process

The term "mitosis" was coined by German anatomist Walther Flemming in 1882. It derives from the Greek word "mitos," meaning "warp thread," referencing the thread-like appearance of condensing chromosomes. Alternative terms like "karyokinesis" (nuclear division) and "equational division" have also been used.[23][24]

Stages of Mitosis

Preprophase (Plants)

Unique to plant cells, this stage involves the migration of the nucleus to the cell center and the formation of a preprophase band of microtubules, marking the future division plane. This occurs before prophase begins.[38]

Prophase

Chromatin fibers condense into visible chromosomes, each consisting of two sister chromatids joined at the centromere. The nucleolus disappears, and the mitotic spindle begins to form from centrosomes.[40]

Prometaphase

The nuclear envelope disintegrates (in open mitosis), allowing microtubules to invade the nuclear space. Kinetochore microtubules attach to chromosomal kinetochores, initiating chromosome movement.[45]

Metaphase

Centrosomes reach opposite poles, and chromosomes align along the metaphase plate at the cell's equator. The spindle assembly checkpoint ensures proper attachment and alignment before proceeding.[49][51]

Anaphase

Sister chromatids separate, becoming daughter chromosomes. These are pulled towards opposite poles by shortening kinetochore microtubules, while polar microtubules elongate the cell.[52]

Telophase

This stage reverses prophase events. New nuclear envelopes form around the separated chromosome sets, which decondense. The cell elongates further, and the nucleoli reappear, completing nuclear division.[54]

Cytokinesis: Completing Division

Animal Cells

In animal cells, cytokinesis involves the formation of a cleavage furrow. A contractile ring of actin and myosin pinches the cell membrane inward between the two nuclei, eventually separating the cytoplasm into two daughter cells.[55]

Plant Cells

Plant cells form a cell plate in the center of the phragmoplast, derived from Golgi vesicles. This cell plate develops into a new cell wall, dividing the parent cell into two daughter cells.[39]

Multinucleated Cells

In some organisms and specific cell types, mitosis may occur without subsequent cytokinesis, leading to the formation of multinucleated cells, known as coenocytes.[57]

Biological Significance

Growth and Development

Mitosis is fundamental for the growth of multicellular organisms, increasing cell numbers from a single zygote to a complex body. It also facilitates the replacement of old or damaged cells, maintaining tissue integrity.[58]

Repair and Renewal

Many tissues, like skin and the digestive tract lining, constantly shed cells. Mitosis ensures a continuous supply of new, genetically identical cells to replace those lost, crucial for healing and tissue maintenance.[58]

Asexual Reproduction

For many unicellular organisms and some multicellular ones, mitosis is the primary mode of asexual reproduction. It allows for the creation of genetically identical offspring, ensuring rapid population growth under favorable conditions.[59]

Variations in Mitosis

Forms of Division

Mitosis varies across eukaryotes based on nuclear envelope behavior (open, closed, semiopen) and spindle symmetry (orthomitosis, pleuromitosis). Closed intranuclear pleuromitosis is considered the most primitive form.[9]

  • Closed Intranuclear Pleuromitosis: Typical in Foraminifera, fungi, and some protists.
  • Closed Extranuclear Pleuromitosis: Found in Trichomonadida and Dinoflagellata.
  • Closed Orthomitosis: Observed in diatoms, ciliates, yeasts, and some fungi.
  • Semiopen Pleuromitosis: Characteristic of most Apicomplexa.
  • Semiopen Orthomitosis: Seen in some amoebae and green flagellates.
  • Open Orthomitosis: Common in mammals, metazoa, and land plants.

Mitotic Errors

Errors like nondisjunction (failure of sister chromatids to separate) or anaphase lag (chromatid lagging behind) can lead to aneuploidy (abnormal chromosome numbers). Endoreduplication occurs when chromosomes duplicate but the cell fails to divide, resulting in polyploid cells.[68]

  • Nondisjunction: Leads to trisomy or monosomy in daughter cells.
  • Anaphase Lag: Results in a lost chromatid and a monosomic daughter cell.
  • Endoreduplication: Chromosome duplication without cell division, leading to polyploidy.
  • Endomitosis: Chromosome replication within an intact nucleus, increasing chromosome number.

Diagnostic Significance

The rate and appearance of mitosis (mitotic index) are crucial diagnostic markers in histopathology, particularly for assessing tumor aggressiveness. Atypical mitotic figures can indicate high-risk conditions.[74][75]

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References

References

  1.  "Notes and memoranda: The late professor von Mohl". Quarterly Journal of Microscopical Science, v. XV, New Series, p. 178รขย€ย“181, 1875. link.
  2.  Bernstein, H., Bernstein, C. Evolutionary origin and adaptive function of meiosis. In "Meiosis", Intech Publ (Carol Bernstein and Harris Bernstein editors), Chapter 3: 41รขย€ย“75 (2013).
A full list of references for this article are available at the Mitosis Wikipedia page

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