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CSF Exam 3
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variation of the cell cycle
different organisms and different cell types within an organism spend different amounts of time in these phases
G1 major function
cell growth
G1 activities
perform regular cellular functions (different in specialized cells)
make proteins and organelles
G1 checkpoint
adjust if something has gone wrong
point where the cell commits to entering cell cycle OR a quiscent state (check internal/external conditions)
reasons to go dormant
DNA damage
size check
nutrient check
function
G0
pause
no longer actively dividing but they maintain metabolic activity
not "dormant" but functional
temporary or permanent
differentiated neurons
stem cells differentiate into neurons and also have self proliferation
its best that not all neurons actively divide
to protect the complex
lack necessary organelles for cell division
reasons for differentiated neurons
dividing neurons could disrupt neural network
loss of learning and memory
what if they don't pass a checkpoint and enter apoptosis
stem cell DO enter G0
quiescent stem cells
mtor
a protein kinase that acts as regulator of cell growth, proliferation, and metabolism by responding to environmental cues (nutrients and growth factors
overactivation of certain pathways can lead to cell death (apoptosis) rather than repair (autophagy)
mtor
quiscent stem cell may differentiate into the wrong type of cells
make lots of glial cells and not mature neurons
S phase - synthesis major function
prepare for cell division
S phase synthesis activities
DNA replication
centrosome replication (begins)
centrosome organelle
microtubule organizing centers that form spindles during cell division
two perpendicular centrioles
DNA replication - major activity in synthesis
enzyme: DNA polymerase
function: synthesize DNA
steps: intiation, elongation, termination
DNA replication initiation
unwind DNA (helicase)
prevent supercoiling using topoisomerase
prevent re-annealing/back together (SSBP)
DNA replication elongation
make short RNA primers (primase)
synthesize new strands off the primers (DNA polymerase)
leading strand
cont 5' to 3'
lagging strand
discontinuous okazaki fragments
DNA replication termination
reach the end of chromosome synthesis
primers removed and new pieces synthesized by polymerase
fragments joined by DNA ligase
(don't have full okazaki fragments)synthetic DNA replication
synthetic DNA replication
polymerase chain reaction PCR - copying DNA in vitro
in vivo cloning
method uses living organisms (bacteria) to replicate gene of interest
1. restriction enzyme cut desired gene from chr and to open circular DNA molecule called vector (plasmid)
2. gene of interest and vector joined together by ligase creating recombinant DNA molecule
3. recombinant DNA is then introduced into bacterial cells
4. as bacteria reproduce, they replicate the recombinant DNA, creating a large number of identical copies of the gene of interest within a clone of bacterial cells
in vitro PCR
amplifies DNA in a test tube w out living cels
1. dsDNA with gene of interest heated to separate strands
2. primers (short DNA seq) bind to ends of gene of interest
3. DNA polymerase syntheizes new complementary DNA strands doubling the amount of DNA
4. repeated in thermal cycler and end up with lots of copies
steps of PCR
1. denature - high heat unwind DNA
2. annealing - specific primers low temp
3. extension - middle temp polymerase adds nucleotides (dNTPs)
when do you have a higher denaturing temp
when you have more GC pairs
longer fragment annealing/denaturation
need longer annealing and denaturation to ensure complete strand separation and efficient primer binding
PCR components
template (thing to be copied)
primers (designed for specific piece)
polymerase (to build the strand)
dNTPs (building blocks)
buffer (keep everyone happy)
G2 major function
grow and make more stuff
prepare for mitosis
G2 activities
make new proteins and organelles
newly duplicated centrosome matures
G2 checkpoint
check for
DNA damage
size check
proper replication
mitosis phase general
mitosis + cytokinesis
mitosis goal
make an identical cell
want a full sel of maternal and paternal chr
chromatid
one of two identical halves of a chromosome
chromosomes are duplicated in S phase
sister chromatids stay paired until separation in mitosis
prophase
condensing the cells
breakdown of nuclear membrane starts (no longer cont)
chr are visible and being to form in nucleus
metaphase
sister chromatids line up along the metaphase plate
nuclear membrane is gone
anaphase
sister chromatids move to opposite poles
early and late anaphases
telophase
nuclear envelope/nucleolus reforms
chromosomes decondense
major players in PMAT
microtubules and centrosomes
prophase major role
centrosomes move to opposite poles and spindle formation begins
prometaphase
spindles attach to chromosomes at the kinetochore
metaphase major role
mitotic spindles are attached and help with orientation/alignment at the metaphase plate
anaphase major role
mitotic spindles help pull chr apart
telophase major role
mitotic spindles have finished their job and are broken down
cytokinesis major function
make two cells
cytoskeleton is the star of the show!
cytokinesis activities
material will split bt cells and a new membrane gets created resulting in two daughter cells
mechanism of cytokinesis
1. microtubules which form the spindle fibers -- signal where the cell will divide (cleavage site)
2. actomyosin ring formed by actin filaments and myosin motor proteins -- contracts to pinch cell in half
failure to enter/stay in G0
this can lead to apoptosis
you cannot make mitochondria from scratch
mitochon made from mitochon
made from mitochondrial fission and fusion
rest of the cell made from golgi (and previosuly mito)
g1: functioning normaly
S/g2: double in size, dissociate from centrosome
g2/prophase: fragments from ribbon structure to small clusters that form stacks —> formation of stacks is g2 checkpoint
metaphase: fragment further into golgi haze
anaphase: disperse
telophase: reassemble
more of the rest of the cell in ER
g1: functioning normaly
s: expansion
g2: lots of grwoth anf function (prep for division)
mitosis
- nuc envelope breaks down and fuses w ER
- structural rearrangement occurs to mostly tubular structure but it stays unified through mitosis
- telophase forms new nuc envelopes and goes back to original form
meiosis is a special type of cell division that takes place in gametes
gaol is to facilitate recombination and sometimes produce different types of cells
what facilitates recombination
the synaptonemal complex
zipper like bridge bt homo chr during prophase 1 holding them together for genetic exchange
male meiosis
four functional sperm cells made by equal division
female meiosis
meiosis 1 assymetrical cell division -- one occyte and 3 polar bodies
selfish genetic elements
increase their own transmission to the next generation even if it harms the organism
female meiosis is a great place to be selfish
want to be in oocyte not polar body