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what was the significance of xenopus cytoplasm in discovering cell cycle regulation?
there were stopping points found between cell cycle phases, when cytoplasm from meiosis II cells were inserted into cells in G2, there were no stops indicating there was something present in the cytoplasm regulating activity
what was the significance of the cell cycles in sea urchins?
they found that expression of a certain protein (cyclins) were synonymous with a certain phase of the cell cycle
MPF
cyclin/CDK complex for M-phase, M-cyclin and Cdc2
Cdc2
CDK for M-phase, regulates cell division
how is Cdc2 activated?
it binds to M-cyclin, which allows it to be phosphorylated
what two molecules regulate Cdc2 activation?
Wee1 and Cdc25
where does phosphorylation occur on Cdc2?
T14/Y15, blocks the activation site
what are three substrates the MPF phosphorylates to regulate M-phase?
nuclear filaments/lamins, microtubule associated proteins (MAP), and anaphase promoting complex (APC)
what happens when MPF phosphorylates nuclear filaments?
it leads to the breakdown of the nuclear envelope during prophase/prometaphase
what happens when MPF phosphorylates MAP?
leads to microtubule reorganization so that spindles can form
what happens when MPF phosphorylates APC?
targets M-cyclin for degradation to stop the cell from dividing again
APC
ubiquitinator protein, helps regulate cell division by degrading m-CDK and cleaves cohesion proteins that hold chromosomes together
Sec1
cohesion proteins that keep sister chromatids attached
separase
cleaves Scc1
securin
binds to separase to prevent cleavage of cohesion proteins until it is time for division
how does APC regulate sister chromatid division?
when phosphorylated, it ubiquitinates securin, activating separase
G2 checkpoint
DNA damage checkpoint before cell enters M-phase
what happens when DNA damage is detected at the G2 checkpoint?
cdc25 is inhibited, which prevents M-CDK activity and division
M-checkpoint
checks to make sure there is proper spindle attachment at the centromere
Mad2
protein that inhibits APC by binding to unattached kinetochores to prevent premature chromosome separation