Cell Division, Mitosis, and Meiosis Flashcards

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Vocabulary flashcards covering cell division, the cell cycle, mitosis, meiosis, chromosomal abnormalities, and cancer regulation.

Last updated 1:31 AM on 9/2/26
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40 Terms

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Cell Division

The process by which one parent cell produces new cells, which is essential for growth, repair of damaged tissues, replacement of worn-out cells, and reproduction.

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Cell Cycle

The ordered sequence of events that prepares a cell for division and results in two daughter cells, divided into Interphase and Mitotic Phase (M Phase).

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Interphase

The phase occupying about 90%90\% of the cell cycle during which the cell grows, performs normal functions, duplicates DNA, and prepares for division.

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G1G_1 Phase (First Gap)

The subphase of interphase where the cell increases in size, organelles multiply, proteins are synthesized, energy is stored, and normal metabolism is performed.

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S Phase (Synthesis)

The subphase of interphase where DNA is replicated, centrosomes duplicate, and every chromosome becomes two identical sister chromatids.

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G2G_2 Phase (Second Gap)

The subphase of interphase where the cell continues growing, DNA is checked for errors, and proteins needed for mitosis (such as spindle proteins) are produced.

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G0G_0 Phase

A resting stage outside the cell cycle entered by non-dividing cells, such as neurons and cardiac muscle cells.

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Karyokinesis

The division of the cell nucleus during the mitotic phase.

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Cytokinesis

The division of the cytoplasm that completes cell division to produce two genetically identical daughter cells.

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G1G_1 Checkpoint

An internal quality-control checkpoint that checks if the cell is large enough, if nutrients are available, and if DNA is damaged before allowing entry into S phase.

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G2G_2 Checkpoint

An internal quality-control checkpoint that verifies whether DNA has been completely copied and is undamaged before entering mitosis.

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M Checkpoint (Spindle Checkpoint)

An internal checkpoint that verifies if all chromosomes are attached to spindle fibers correctly before anaphase begins.

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Cyclins

Proteins whose concentration rises and falls during the cell cycle to regulate progression through each phase.

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Cyclin-Dependent Kinases (CDKs)

Enzymes activated by cyclins that phosphorylate target proteins to push the cell into the next phase of the cell cycle.

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Mitosis

Nuclear division that produces two genetically identical diploid (2n2n) daughter cells from body (somatic) cells.

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Cleavage Furrow

A groove formed by a contractile ring of actin in animal cells during cytokinesis that pinches the cell into two daughter cells.

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Cell Plate

A structure formed from Golgi vesicles in plant cells during cytokinesis that develops into a new cell wall between daughter cells.

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Nondisjunction

The failure of sister chromatids to separate properly during mitosis or meiosis, resulting in one daughter cell with an extra chromosome (n+1n+1) and one with a missing chromosome (n1n-1).

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Down Syndrome (Trisomy 21)

A trisomy disorder where the 21st chromosome has three instead of two chromosomes, often characterized by a short neck with excess skin, flattened facial profile, small head, ears, and mouth, and upward slanting eyes.

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Edward Syndrome (Trisomy 18)

A condition caused by an additional copy of chromosome 18, characterized by cleft palate, clenched fists, deformed feet, low-set ears, chest deformity, and severe developmental delays.

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Patau Syndrome (Trisomy 13)

A genetic disorder caused by an additional copy of chromosome 13, manifesting as cleft lip or palate, extra fingers or toes (polydactyly), low-set ears, small head, and hernias.

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Klinefelter Syndrome (47,XXY47, \text{XXY})

A condition resulting from two or more X chromosomes in males, primarily characterized by infertility and small, poorly functioning testicles.

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Trisomy X Syndrome (47,XXX47, \text{XXX})

A condition characterized by the presence of an extra X chromosome in each cell of a female, where affected individuals are often taller than normal with mild or no symptoms.

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Turner Syndrome (45,XO45, \text{XO})

A condition affecting females where one X chromosome is missing or partially missing, physically characterized by a webbed neck, short stature, and swollen hands and feet.

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Mosaicism

A genetic situation occurring when a mutation happens during mitosis in an early cell of a developing organism, causing only the cells derived from that mutated cell to carry the mutation.

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Cancer

A disease in which cells lose normal control over the cell cycle, allowing them to divide uncontrollably, ignore checkpoints, and avoid cell death.

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Mutation

A permanent change in DNA caused by radiation, UV light, cigarette smoke, certain chemicals, viruses, or random DNA replication errors.

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Proto-oncogenes

Normal genes that promote cell growth and division and are necessary for normal development.

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Oncogenes

Mutated forms of proto-oncogenes that continuously stimulate cell division.

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p53 Protein

Known as the 'Guardian of the Genome,' a tumor suppressor protein that stops the cell cycle, activates DNA repair, or initiates apoptosis if repair fails.

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p21 Protein

A protein that blocks cyclin-dependent kinases (CDKs), preventing the cell from entering S phase until DNA is repaired.

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Tumor Suppressor Genes

Genes that slow or stop the cell cycle, repair DNA, trigger apoptosis, and prevent uncontrolled cell growth (e.g., p53, Rb, p21).

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Apoptosis

The controlled, programmed destruction of damaged or unnecessary cells, during which the cell breaks into apoptotic bodies that are safely removed by immune cells.

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Benign Tumor

A non-cancerous mass of abnormal cells that does not invade nearby tissues and usually remains localized.

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Malignant Tumor

A cancerous mass of abnormal cells that invades nearby tissues and can spread through blood or lymph.

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Metastasis

The spread of cancer cells from a primary malignant tumor to other parts of the body.

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Meiosis

A two-step cell division process that produces four haploid gametes (sperm or egg cells) from a single diploid cell.

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Crossing Over

The process during prophase I of meiosis in which homologous chromosomes trade parts, creating new combinations of alleles.

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Synaptonemal Complex

A protein structure that holds homologous chromosomes together during crossing over in prophase I of meiosis.

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Chiasmata

Cross-shaped structures visible under a microscope where homologous chromosomes remain linked together after the synaptonemal complex breaks down.