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Wong_Katrina_Block5_MM8 (cell cycle control system - molecules in a cell…
Wong_Katrina_Block5_MM8
asexual: individual = sole parent, genomes of offspring are exact copies of parents (clone)
mitosis
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Mitosis
prophase
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- duplicated chromosome --> 2 sister chromatids
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- centrosomes part, propelled by the lengthening microtubules between them
prometaphase
- nuclear envelope fragments
- microtubules of spindle invade nuclear area & interact w chromosomes
- microtubules extend from each chromosome
- each of the 2 chromatids of a chromosome has a kinectochore (@centromere)
- some of microtubules attach to the kinectochores-->kinectochore microtubules (jerk chromosomes back and forth)
- non kinectochore microtubules interact w those from opposite poles of spindle
metaphase
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- centrosomes are at opposite ends
- chromosomes (centromere) convene on metaphase plate
- per chromosome, kinectochores of sister chromatids are attached to kinectocchore microtubules coming from opposite poles
- full apparatus of microtubules = spindle because of shape
anaphase
- =shortest stage of mitosis
- begins when 2 sister chromatids of each pair suddenly part, each chromatid --> full fledged chromosome
- 2 free chromosomes begin moving to opposite ends of the cell, as kinectochore microtubules shorten
- cell elongates as nonkinectochore microtubules lengthen
- by the end, 2 ends of cell have equivalent & complete collections of chromosomes
telophase + cytokinesis
- 2 daughter nuclei begin to form in the cell
- nuclear envelopes arise from fragments of parent's and other parts of endomembrane system
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- chromosomes become less condensed
- division of cytoplasm is usually well underway by late telophase, so 2 daughter cells appear shortly after end of mitosis
- in animal cells, cytokinesis involves the formation of a cleavage furrow, which pinches cell in two
binary fission
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genes are carried on a single bacterial chromosome that consists of a circular DNA molecule & associated proteins
DNA begins replicating at origin of replication, producing 2 origins. the cell elongates, grows inward and splits
sexual: 2 parents give rise to offspring w unique combinations of of genes; genetic variation from parents and siblings
meiosis
interphase
- chromosomes replicate during S phase but stay uncondensed
- each replicated chromosome has 2 genetically identical sister chromatids
- centrosome replicates, forming 2 centrosomes
meiosis 1
metaphase 1
- pairs of homologous chromosomes (as tetrads) arrange on metaphase plate, w one chromosome per pair facing each pole
- both chromatids of a homologue = attached to kinetochore microtubules from one pole; those of the other homologue are attached to microtubules from the opposite pole
anaphase 1
- chromosomes move to poles, guided by spindle apparatus
- sister chromatids stay to the centromere & move as a unit to the same pole
- homologous chromosomes, each w 2 sisters, move to opposite poles
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prophase 1
- takes up 90% of time for meiosis
- chromosomes begin to condense
- homologous chromosomes loosely pair along their lengths, precisely aligned gene by gene
- in crossing over, DNA molecules in nonsister chromatids break at corresponding places, then rejoin too the others DNA
- in synapsis, synaptonemal complex (protein structure) forms between homologues, holding em together along their lengths
- each tetrad has 1+ chiasmata (criss-crossed regions where crossing over occurred) holds homologues together til anaphase 1
- movement of centrosomes, formation of spindle microtubules, break down of nuclear envelope, dispersal of nucleoli
- late prophase 1: kinectochores per homologue attach to microtubules from one pole/the other. homologues move --> metaphase plate
meiosis 2
metaphase 2
- chromosomes are positioned on metaphase plate as in mitosis
- 2 sister chromatids of each chromosome aren't genetically identical cuz of crossing over
- kinectochores of sister chromatids are attached to microtubules extending from opposite poles
anaphase 2
- centromeres of each chromosome finally separate, the sister chromatid comes apart
- sister chromatids of each chromosome now move as 2 individual chromosomes toward opposite poles
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prophase 2
- a spindle apparatus forms
- in late prophase 2, chromosomes made of 2 chromatids move to metaphase 2 plate
genetic variation
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crossing over
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occurs in early prophase 1. 2 nonsisters (maternal and praternal of a homologous pair) are broken at the some place and rejoined to each others DNA.
@ metaphase 2, chromosomes w 1+ recombinant chromatids can be oriented in 2 alternative, non equivalent ways bc their sister chromatids are no longer identical twins. this independent assortment increases variability
random fertilization
random nature of fertilization (each gamete reps 1/8 mil possible chromosome combinations due to independent assortment during meiosis, fusion w a female gamete = 1/64mil)
cell cycle control system - molecules in a cell that triggers/coordinates key events in the cell cycle
G1 check point
complete S, G2, M and divide
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IN CANCER
- dont stop when growth factors are depleted (may make their own, or abnormality in sigaling pathway conveys factors signal in absence of it/abnormal cell cycle control system)
- cancer cells stop growing @ random points, rather than @ checkpoints, can divide indefinitely w unlimited nutrients
problem begins w transformation - normal cell --> cancer cell. normally destroyed w immune system. if cell evades destruction --> proliferate --> tumor
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