Cell Communication, Cell Cycle, Mitosis, and Meiosis

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Comprehensive vocabulary flashcards covering cell signaling pathways, cell cycle checkpoints and cancer regulation, and meiotic cell division from Chapters 11, 12, and 13.

27 Terms

1
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Ligand

A signaling molecule that specifically binds to a receptor protein, causing the receptor to change shape and initiate cellular transduction.

2
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G Protein-Coupled Receptor (GPCR)

A universal cell-surface transmembrane receptor that functions with the aid of a G protein; approximately 50%50\% of all commercial drugs target this family of receptors.

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Cyclic AMP (cAMP)

A small, water-soluble second messenger synthesized from ATP by adenylyl cyclase that activates protein kinase A (PKA) to trigger cellular responses.

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Phosphodiesterase

An intracellular enzyme that terminates signaling by hydrolyzing cyclic AMP (cAMP) into inactive AMP using H2O\text{H}_2\text{O}.

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Receptor Tyrosine Kinase (RTK)

An enzymatic cell-surface receptor that dimerizes upon ligand binding and undergoes auto-phosphorylation on tyrosine residues using ATP to activate relay proteins.

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Herceptin

A monoclonal antibody (mAb) therapy engineered to bind to HER2 receptor tyrosine kinases on breast cancer cells, blocking downstream signaling to inhibit proliferation and flagging cells for immune destruction.

<p>A monoclonal antibody (mAb) therapy engineered to bind to HER2 receptor tyrosine kinases on breast cancer cells, blocking downstream signaling to inhibit proliferation and flagging cells for immune destruction.</p>
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Inositol Trisphosphate (IP3\text{IP}_3)

A second messenger produced by phospholipase C cleavage of PIP2\text{PIP}_2 that binds to and opens ligand-gated calcium channels on the endoplasmic reticulum membrane, releasing Ca2+\text{Ca}^{2+} into the cytosol.

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Intracellular Receptor

A receptor situated in the cytoplasm or nucleus that binds hydrophobic or lipid-soluble signal molecules (such as steroid hormones like testosterone) to form complexes that act directly as transcription factors.

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1986 Nobel Prize in Physiology or Medicine

Awarded jointly to Stanley Cohen and Rita Levi-Montalcini for their foundational discovery of growth factors (such as Nerve Growth Factor, NGF).

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Sister Chromatids

Two identical copies of a duplicated chromosome produced during S phase of interphase, joined along their length and attached at a specialized constriction called the centromere.

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Centromere

The constricted DNA region of a duplicated chromosome where sister chromatids are most closely attached and where kinetochores assemble.

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Mitotic Spindle

A subcellular structure consisting of microtubules and associated proteins (including asters, kinetochore microtubules, and nonkinetochore microtubules) that segregates chromosomes during mitosis.

<p>A subcellular structure consisting of microtubules and associated proteins (including asters, kinetochore microtubules, and nonkinetochore microtubules) that segregates chromosomes during mitosis.</p>
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Maturation-Promoting Factor (MPF)

A cyclin-CDK complex formed when cyclin binds to a cyclin-dependent kinase, triggering cell passage through the G2\text{G}_2 checkpoint into M phase (mitosis).

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Density-Dependent Inhibition

A growth-regulatory phenomenon where normal cultured mammalian cells stop dividing once they form a complete, single layer due to physical cell-cell contact.

<p>A growth-regulatory phenomenon where normal cultured mammalian cells stop dividing once they form a complete, single layer due to physical cell-cell contact.</p>
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Anchorage Dependence

The requirement that animal cells must adhere to a solid substratum or extracellular matrix surface in order to divide.

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Angiogenesis

A biological hallmark of cancer involving the growth of new blood vessels (frequently mediated by VEGF) to supply developing tumors with oxygen and nutrients.

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Oncogenes

Cancer-promoting genes resulting from gain-of-function mutations in proto-oncogenes that cause excessive cellular proliferation (e.g., Ras mutations found in >30%>30\% of all cancers).

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Tumor Suppressor Genes

Genes that encode proteins providing critical 'stop signals' to inhibit cell division or initiate apoptosis; loss-of-function mutations in both copies promote cancer (e.g., p53 mutations present in >50%>50\% of cancers).

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Henrietta Lacks (HeLa Cells)

The source of the first continuously cultured 'immortal' human cell line, obtained without consent in 1951, which transformed modern cellular and medical research.

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Homologous Chromosomes

Pairs of matching chromosomes—one inherited from each parent—that have the same length, centromere location, and carry genes controlling the same inherited characters.

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Karyotype

An ordered display of an individual's paired homologous chromosomes arranged according to length, centromere position, and banding pattern.

<p>An ordered display of an individual's paired homologous chromosomes arranged according to length, centromere position, and banding pattern.</p>
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Meiosis I

The first division of meiosis, termed reductional division, in which homologous chromosomes pair, synapse, cross over, and segregate, reducing chromosome ploidy from diploid (2n2n) to haploid (nn).

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Meiosis II

The second division of meiosis, termed equational division, in which sister chromatids separate, resulting in four genetically distinct haploid (nn) daughter cells.

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Chiasmata

X-shaped microscopic intersection points between nonsister chromatids of homologous chromosome pairs where physical crossing over occurs during prophase I of meiosis.

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Spermatogenesis vs. Oogenesis

Spermatogenesis produces four viable haploid sperm cells continuously from each primary spermatocyte, whereas oogenesis yields only one functional ovum and non-viable polar bodies due to unequal cytokinesis.

<p>Spermatogenesis produces four viable haploid sperm cells continuously from each primary spermatocyte, whereas oogenesis yields only one functional ovum and non-viable polar bodies due to unequal cytokinesis.</p>
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Nondisjunction

An error during cell division in which homologous chromosomes fail to separate in meiosis I or sister chromatids fail to separate in meiosis II, resulting in aneuploid gametes (n+1n+1 and n−1n-1).

<p>An error during cell division in which homologous chromosomes fail to separate in meiosis I or sister chromatids fail to separate in meiosis II, resulting in aneuploid gametes ($$n+1$$ and $$n-1$$).</p>
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Trisomy 21 (Down Syndrome)

An aneuploid condition characterized by the presence of three copies of chromosome 21 (47,21+47, 21+), occurring in approximately 1:7001:700 live births.

<p>An aneuploid condition characterized by the presence of three copies of chromosome 21 ($$47, 21+$$), occurring in approximately $$1:700$$ live births.</p>