AP Bio Ch 4

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Last updated 4:23 AM on 2/4/26
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46 Terms

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direct contact

communications through cell junctions, passing freely through adjacent cells (gap junctions, plasmodesmata)

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local regulators

secreting cells releasing chemical messages (ligands/local regulators) that travel a short distance through extracellular fluid and cause a response in a target cell

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paracrine signaling

secretory cells release local regulators (ie growth factors) via exocytosis to an adjacent cell

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synaptic signaling

neurons secreting neurotransmitters that diffuse across the synaptic cleft (aka the space between the nerve cell and target cell)

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long distance signaling

hormones, endocrine signaling through circulatory system

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cell signaling steps

reception (ligand binds to receptor), transduction (signal is converted), response (cell process is altered)

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reception

detection and receiving of ligand by target cell

  • one area of receptor interacts with ligand and one area transmits a signal to another protein, highly specific bonding

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plasma membrane receptors

most common receptor in signal pathways, binds to polar large water soluble ligands (ex: peptide hormones, GPCRs)

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intracellular receptors

found in the cytoplasm or nucleus of target cell, binds to hydrophobic ligands passed through plasma membrane (ex: steroid and thyroid hormones)

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transduction

conversion of an extracellular signal to an intracellular signal that will bring about a cellular response, requires changes in the signal transduction pathway

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phosphorylation

adding phosphate via ATP or enzyme protein kinase to relay signal inside cell (part of transduction)

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dephosphorylation

removing phosphate by enzyme protein phosphatase, shuts off pathways (part of transduction)

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second messengers

small, nonprotein molecules and ions help relay the message and amplify the response during transduction

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response

final molecule in signaling pathway converts the signal to a response that will alter a cellular process (ex: proteins or enzymes)

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G protein coupled receptors (GPCRs)

largest category of cell surface receptors, important for animals’ sensory systems, binds to a G protein that can bind to GTP (molecule similar to ATP), inactive until ligand binds to it

  • ligand binding changes cytoplasmic side’s shape

  • activates/binds to enzyme, amplifying signals

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ion channels

receptors in plasma membrane that open or close for diffusion of specific ions to start off cellular response events

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negative feedback loop

reduces the effect of the stimulus (ex: heat —> skin receptors —> sweat glands —> sweat), stops when problem is solved

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positive feedback loop

increases the effect of a stimulus (ex: blood clotting, fruit ripening), stops when problem is solved

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centromere

region on each sister chromatid where they are most closely attached

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kinetochore

proteins attached to the centromere that link each sister chromatid to the mitotic spindle

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chromatin

formed by strings of nucleosomes. in a non-condensed form when not dividing, but condenses into a chromosome after DNA replication

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homologous chromosomes

one chromosome from each parent that are the same length, have the same centromere position, and carry genes controlling the same characteristics

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somatic cells

diploid (2n): 2 sets of chromosomes, one set from each parent, divides by mitosis, humans have 46 total (23 from each parent)

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gametes

reproductive cells, haploid (n): one set of chromosomes, divides by meiosis, humans have 23

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interphase

longest portion of cell cycle

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G1 (first gap) phase

cell grows, carries out normal function

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S (synthesis) phase

DNA replication, chromosome duplication occurs

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G2 (second gap) phase

final growth and preparation for mitosis

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mitosis

division of nucleus, results in 2 identical diploid daughter cells

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cytokinesis

cytoplasm divides

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prophase

chromatin condenses, nucleoli disappear, duplicated chromosomes appear as sister chromatids, mitotic spindle forms, centromeres move away from each other

<p>chromatin condenses, nucleoli disappear, duplicated chromosomes appear as sister chromatids, mitotic spindle forms, centromeres move away from each other</p>
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prometaphase

nuclear envelope fragments, microtubules enter nuclear area and some attach to kinetochores

<p>nuclear envelope fragments, microtubules enter nuclear area and some attach to kinetochores</p>
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metaphase

centrosomes are at opposite poles, chromosomes line up at metaphase plate, microtubules are attached to each kinetochore

<p>centrosomes are at opposite poles, chromosomes line up at metaphase plate, microtubules are attached to each kinetochore</p>
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anaphase

sister chromatids separate and move to opposite ends of the cell due to microtubule shortening, cell elongates

<p>sister chromatids separate and move to opposite ends of the cell due to microtubule shortening, cell elongates</p>
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telophase

2 daughter nuclei form, nucleoli reappear, chromosomes decondense

<p>2 daughter nuclei form, nucleoli reappear, chromosomes decondense</p>
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cytokinesis

cleavage furrow appears due to a contractile ring of actin filament in animals, and vesicles produced by the Golgi travel to the middle of the cell and form a cell plate in plants

<p>cleavage furrow appears due to a contractile ring of actin filament in animals, and vesicles produced by the Golgi travel to the middle of the cell and form a cell plate in plants</p>
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G1 checkpoint

most important, checks for cell size, growth factors, and DNA damage, gives go/stop signal

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G2 checkpoint

checks for completion of DNA replication and DNA damage

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apoptosis

programmed cell death

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M (spindle) checkpoint

checks for microtubule attachment to chromosomes at the kinetochores at metaphase

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cyclins

regulatory proteins that control the cell cycle by binding to and activating cyclin-dependent kinases

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cyclin-dependent kinases

enzymes that are only active when its specific cyclin is present, constant concentration throughout cell cycle

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growth factors

hormones released by cells that stimulate cell growth, initiates signal transduction pathway

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contact (or density) inhibition

cell surface receptors recognize contact with other cells, initiates signal transduction pathway that stops the cell cycle in G1 phase

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anchorage dependence

cells rely on attachment to other cells or the extracellular matrix to divide

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cancer cells

don’t follow checkpoints, divide infinitely, evade apoptosis and continue dividing with cell errors