Mitosis Calculators
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Phases of Mitosis
- Prophase: Chromosomes condense and become visible; centrosomes migrate to poles; mitotic spindle begins to form; nuclear envelope begins to break down
- Prometaphase: Nuclear envelope fully breaks down; kinetochore microtubules attach to kinetochores on centromeres; chromosomes begin moving
- Metaphase: Chromosomes align at the metaphase plate (cell equator); spindle assembly checkpoint verifies all kinetochores attached before proceeding
- Anaphase: Cohesins cleaved by separase → sister chromatids separate; kinetochore microtubules shorten → chromatids pulled to opposite poles; cell elongates
- Telophase: Chromosomes arrive at poles; nuclear envelopes reform; chromosomes decondense; cytokinesis begins (cleavage furrow in animal cells; cell plate in plant cells)
Spindle Assembly Checkpoint (SAC)
Ensures all kinetochores are properly attached to spindle microtubules before anaphase begins. Mad1/Mad2 proteins: unattached kinetochore → inhibits APC/C → delays anaphase. SAC failure → chromosome missegregation → aneuploidy → cancer.
Glossary
Frequently Asked Questions
Mitosis is the nuclear division process that produces two genetically identical daughter cells. Phases: Prophase: chromosomes condense; centrosomes move apart; spindle begins forming. Prometaphase: nuclear envelope breaks down; spindle microtubules capture chromosomes at kinetochores. Metaphase: chromosomes align at the metaphase plate; spindle assembly checkpoint (SAC) verifies all kinetochores are attached. Anaphase: cohesin cleaved by separase → sister chromatids separate → pulled to opposite poles by shortening kinetochore microtubules. Telophase: chromosomes at poles; nuclear envelopes reform; chromosomes decondense. Cytokinesis: cytoplasm divides (animal: cleavage furrow; plant: cell plate formation by vesicle fusion at the phragmoplast).
The spindle is a bipolar structure made of microtubules (α/β-tubulin polymers) emanating from two spindle pole bodies (centrosomes in animal cells; without centrosomes in plant cells). Kinetochore microtubules: attach to the kinetochore protein complex at the centromere of each sister chromatid. Sister chromatids: held together by cohesin complexes (ring proteins encircling the two chromatid arms). Metaphase: tension from both poles' microtubules aligns chromosomes at the equator. Anaphase: separase enzyme cleaves the Scc1/Rad21 subunit of cohesin → cohesins release → sister chromatids separate. Kinetochore microtubules shorten from the plus end → chromatids are reeled to the poles. Cell elongates via polar microtubule sliding (kinesin-5 pushes anti-parallel microtubules apart).
Mitosis vs. meiosis: Mitosis: one cell → two identical daughter cells; diploid → diploid (2n → 2n); no crossing over; sister chromatids separate; used for growth, repair, asexual reproduction. Meiosis: one cell → four genetically unique haploid cells; diploid → haploid (2n → n); crossing over (recombination) in meiosis I; homologous chromosomes separate in meiosis I; sister chromatids separate in meiosis II; produces gametes (sperm, eggs) or spores. Meiosis consists of two rounds of division (meiosis I and II); mitosis has one. Meiosis is only in germ cells (gonads); mitosis is in all somatic cells.
The spindle assembly checkpoint (SAC) is a cell cycle control mechanism ensuring all kinetochores are properly attached to spindle microtubules before sister chromatid separation (anaphase) begins. How it works: unattached or incorrectly attached kinetochore → Mad1 recruits Mad2 → Mad2 inhibits Cdc20 (activator of APC/C) → APC/C cannot trigger separase → cohesin stays intact → anaphase blocked. Once all kinetochores are bioriently attached: checkpoint is satisfied → APC/C activated → securin degraded → separase active → cohesin cleaved → anaphase begins. SAC failure: chromosome missegregation → aneuploidy (wrong chromosome number in daughter cells). Aneuploidy is a hallmark of cancer cells and causes Down syndrome, trisomy 18, and other chromosomal disorders.