SG

Cell Cycle & Cell Division – Comprehensive Study Notes

Origin & Importance of Cell Division

  • Every multicellular organism begins as a single cell (zygote); through successive divisions, one cell becomes millions.
  • Division must be orchestrated with DNA replication and cell growth to ensure intact genomes in progeny.
  • Growth, tissue repair, reproduction, and the maintenance of chromosome number across generations all hinge on regulated cell cycles.

Definition & Scope of the Cell Cycle

  • Cell cycle = ordered sequence that duplicates DNA, enlarges cytoplasm, and partitions everything into two daughter cells.
  • Two overarching phases:
    • Interphase (prep phase between M phases)
    • M phase / Mitotic phase (actual division)
  • Duration examples
    • Typical cultured human cell: \approx 24\text{ h} total; M phase only \approx 1\text{ h}; Interphase > 95\% of cycle.
    • Budding yeast: entire cycle \approx 90\text{ min}.

Interphase – Detailed Sub-phases

  • G1 (Gap 1)
    • From end of mitosis to start of DNA replication.
    • Intense metabolic activity, continuous growth, normal function.
    • Organelle duplication largely occurs here.
    • DNA amount: constant (denote as 2C), chromosome number 2n.
  • S (Synthesis)
    • Complete DNA replication → DNA content doubles: 2C \rightarrow 4C.
    • Chromosome number stays 2n; each chromosome gains a sister chromatid.
    • Centriole duplication in animal cells.
  • G2 (Gap 2)
    • Protein synthesis for mitosis; further cytoplasmic growth.
    • DNA content remains 4C until mitosis starts.
  • G0 (Quiescent stage)
    • Cells exit G1, remain metabolically active but non-dividing (e.g., heart muscle, many neurons).
    • Can re-enter the cycle on demand (wound healing, etc.).

Control, Variations & Special Cases

  • Animals: mitosis normally occurs in diploid somatic cells; exception – haploid males of honey-bee (drones) divide mitotically.
  • Plants: mitosis occurs in both diploid and haploid stages (e.g., gametophyte mitoses during alternation of generations).
  • Continuous division tissues
    • Plants: apical & lateral meristems.
    • Animals: no direct meristem equivalent; however stem-cell niches (e.g., bone-marrow hematopoietic stem cells) perform analogous roles.

M Phase – Karyokinesis + Cytokinesis

  • Also called equational division (chromosome number maintained).
  • Four seamlessly progressive stages:

Prophase

  • Follows S & G2; chromatin condensation begins → discrete chromosomes.
  • Each chromosome: two sister chromatids joined at a centromere.
  • Centrosomes (duplicated in S) migrate to opposite poles; each forms an aster; asters + spindle fibres = mitotic apparatus.
  • Disappearance of nucleolus, ER, Golgi, and nuclear envelope marks late prophase.
  • Example calculation (onion root tip, 16 chromosomes):
    • G1: 16 chromosomes, 2C DNA.
    • After S: 16 chromosomes, 4C DNA.
    • Post-M phase daughter cells: 16 chromosomes, 2C DNA each.

Metaphase

  • Nuclear envelope fully disintegrated; chromosomes attain maximal condensation.
  • Kinetochores (protein discs on centromeres) attach to spindle microtubules.
  • Chromosomes align on the metaphase plate; one chromatid connected to each pole.

Anaphase

  • Centromeres split simultaneously; sister chromatids (now daughter chromosomes) pulled toward opposite poles.
  • Centromere leads, arms trail.

Telophase

  • Chromosomes reach poles → decondense; individuality lost.
  • Re-formation of nuclear envelope, nucleolus, ER, Golgi.

Cytokinesis

  • Animal cells: cleavage furrow constricts from periphery inward.
  • Plant cells: cell plate forms centrally → new middle lamella & walls.
  • Failure of cytokinesis after karyokinesis → multinucleate syncytium (e.g., coconut liquid endosperm).

Significance of Mitosis

  • Produces genetically identical diploid daughters → growth of multicellular body.
  • Restores optimum nucleo-cytoplasmic ratio disturbed by cell enlargement.
  • Enables continuous replacement & repair (epidermis, gut lining, blood, meristems).

Meiosis – Overview

  • Specialized division that halves chromosome number to form haploid gametes/spores; fertilization later restores diploid state.
  • Key hallmarks:
    1. Two sequential divisions (meiosis I & II) but one S phase.
    2. Homologous pairing (synapsis) and crossing-over between non-sister chromatids.
    3. Result: four genetically distinct haploid cells.

Meiosis I – Reductional Division

Prophase I (longest, 5 sub-stages)

  1. Leptotene – chromosomes start becoming visible; gradual condensation.
  2. Zygotene – homologues pair (synapsis); formation of synaptonemal complex → unit called a bivalent/tetrad.
  3. Pachytene – clearly visible tetrads; appearance of recombination nodules; crossing-over catalyzed by recombinase enzyme → genetic exchange.
  4. Diplotene – synaptonemal complex dissolves; homologues begin to separate but remain connected at chiasmata (X-shaped crossover sites). In many vertebrate oocytes diplotene arrest can last months/years.
  5. Diakinesis – terminalization of chiasmata; maximum condensation; spindle assembly; nuclear envelope & nucleolus disappear → metaphase I transition.

Metaphase I

  • Bivalents orient on equatorial plate; kinetochore microtubules attach to homologues from opposite poles.

Anaphase I

  • Homologous chromosomes separate (disjunction); sister chromatids remain joined.

Telophase I & Cytokinesis

  • Reappearance of nuclear envelope & nucleolus; produces dyad (two haploid cells with duplicated chromosomes).
  • Brief interkinesis (no DNA replication) precedes meiosis II.

Meiosis II – Equational Division (mitosis-like)

Prophase II

  • Nuclear envelope breaks again; chromosomes (still of two chromatids) re-condense.

Metaphase II

  • Chromosomes align at equator; kinetochores of sister chromatids attach to opposite poles.

Anaphase II

  • Centromeres split; sister chromatids segregate.

Telophase II & Cytokinesis

  • Chromosomes decondense; nuclei reform; cytokinesis yields a tetrad of haploid cells.

Significance of Meiosis

  • Constancy of chromosome number across generations despite sexual reproduction.
  • Genetic variability via independent assortment & crossing-over → raw material for evolution.

Comparative Snapshot – Mitosis vs. Meiosis (Key Contrasts)

  • Number of divisions: 1 vs 2.
  • DNA replication: once, prior to division(s), in both.
  • Pairing of homologues: absent in mitosis, present in prophase I.
  • Crossing-over: only in meiosis.
  • Chromosome number in products: conserved (diploid) vs halved (haploid).
  • Genetic identity: identical daughters vs unique recombinants.

Practical & Conceptual Questions Raised in Text

  • Continuous growth in plants: Which tissues? (Answer: meristems).
  • Mitosis in haploid organisms (male honey-bee, plant gametophytes).
  • Onion root tip exercise regarding n and C values.
  • Examples of equal vs unequal meiotic products (e.g., microspore tetrad vs oogenesis polar bodies).
  • Can DNA replicate without cell division? (Yes – endoreduplication, polytene chromosomes).
  • Can mitosis occur without prior DNA replication? (No, would compromise genomic integrity).

Numerical & Symbolic References (LaTeX Notation)

  • DNA doubling: 2C \rightarrow 4C during S.
  • Human cell-cycle span: \approx 24\text{ h}; M phase \approx 1\text{ h}.
  • Yeast cycle: \approx 90\text{ min}.
  • Onion root example: 16 chromosomes per somatic nucleus.

Real-World & Evolutionary Connections

  • Cancer originates from loss of cell-cycle control.
  • Plant breeding exploits meiotic recombination for new trait assortments.
  • Endosperm syncytium (coconut water) arises via nuclear divisions without cytokinesis.

Ethical & Philosophical Notes

  • Understanding cell division informs stem-cell therapy, cloning, fertility treatments.
  • Balancing medical intervention (e.g., anticancer mitotic inhibitors) with potential side-effects on healthy dividing cells is an ongoing ethical challenge.