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25 Cards in this Set

  • Front
  • Back
Cel cycle
contents of cell must be duplicated before dividing
contents must be distributed into two physically separate cells
Why are these topics important?
-key mechanisms underlying the inheritance of all phenotypic traits
-mitosis= critical for embroynic development, wound healing
-meiosis= increases genetic variation
-meiosis= allows us to identify the genes underlying traits
-problems with these two = cancer and defects
Cell division in Eubacteria and Eukaryotes
Eubacteria: no nucleus, one chromo, no organelles
(simpler process overall)

Eukaryotes: nucleus surrounds the genetic material, multiple chormos need to be segregated correctly, organelles need to be replciated, and control of division is crucial
steps of cell division in eubacteria
cell grows, dna is replicated, and then divided when the rigng around middle tightens and splits apart
Eukaryotic cell cycle
Interphase: time between mitoses
-G1= cell growth
-S= dna replication
-G2=preparation for mitosis
mitosis: once cell separates into two
Mitosis
THIS STEP HAS TO BE PERFECT
-perfect segreattion of chromosomes and centrioles
-two cells produced, each diploid
Overview of Mitosis
prophase, metaphase, anaphase, telophase, and cytokinesis
Duplication of Centrioles
each cell has one centriole pair
centrioles become poles of spindle during mitosis
Division of Mito
Own genome. dont have S phase. they have circular dna and are decendents of bacteria
-several copies of mito dna
-replication happens whenver
-not tied to physical division
-protein dnm1= makes a laso that pinches middle out
-hydrolisis of GTP-GDP squeezes even more
Chromosome Segregation
one from sperm, one from egg.
s phase each is copied= sister chromatids
then these segragate during mitosis
4 Processes Ensure this:
-association and condensation of sister chromatids
-attachement of chromatid pairs to spindle
-separatioin of sister chromatids
-cytokineses into 2 cells
Chromosome pairing and condensing
1. long stretches of interwould alpha helixes (can open or close)
-top is hinge, and attached to openeing is a motor protein= hyrolzie atp and can spring it open or closed

2. either a CAP/ SCC protein regulates when it is open or clsed, recieve infor from cells that control cell cycle
Cohesions
attach sister chromatins during S phase. separate. chohensions are coming around them and clamping daughter strand, hugging the whole length of dna molecule. S phase over, then they are stitched together and held in cohesion.
Condensins
Help chromatin condense= prophase
-open and grab loops of chromosomes
-stabalizes loops
Attachement of sister chromatins
Cohesions wrap around, ssc is regulatonry. kinesan will put them together, and scc clamps on= stitch them together one end to another

a few cohesions remain following condensation. once ready to separate have to break that= separase then cleaves complex at anaphase allowing separation

come ON during S phase, come OFF during anaphase
Mitotic Spindles
composed of many microtubles
pull apart sister chromatids
provide framework for movements during mitosis
Centrioles organize the spindle
anchor the microtubles
-astral: spray out all different directions
-polar: directed towards center and overlap with those from other sides
-kinetochore: attach to chromosomes: pole to chromo
Kinetochore
OPPOSITE DIRECTIONS
-where chromatids attach to mitotic spindle
-link chromatin proteins to microtubules
-multiple microtubules attach to each kinetochore
On right side, all non covalent bonds that lock together
On left side, reach out and interact to grab onto microtubule
Motor proteins that power mitosis
They walk in a specific direction along microtubules

Kinectochore: motor domain carries cargo domain to positive end

Polar: motor movement towards plus end whle the top is going the opposite direction : moves the centrioles apart

Astral: motor movement to minus end on cortex
How do the microtubules move away metaphase plate?
depends on stablilty of structure; tubulin is small and makes dimers between alpha and beta forms= heterodimer
- attache either GTP or GDP to beta subunit, while GTP ismore stable

+ end grows with addition of subunits= more stable
- end shrinks with loss of same
length= balance between gain and loss

- end attaches to centrioles, while + end faces out
how do microtubulins move chromosomes ?
+ end is polymerization, - is depolymerization
-kinetochore proteins switch between these
-k-1 protein promotes the depolymerizatoin at + end
because they need to be plucked away to make room
gets shorter and shorter as more leave and less come in
Metaphase- anaphase transition
when you reach metaphase, starts to move apart
make sure all the chromo are there and attached= they are being pulled on by both poles
-chromatid pairs are condensed, kintetocores attach
-cohesions broken down by separase,
- kinetichores bring to one pole or the other
Cytokinesis
cell pinches off into two
ring of actin and miosin slide past each other, shrink distance, and band and contract pinching them off
Meiosis
One cell (2n)--> one cell (4n) during S phase when each is replicated
First cell division is special: genetic material shuffled and recombined between two sister chromatids
cells divide= SISTER CHROMATIDS DONT SEPARATE. back to 2n-- divide again
-sister chromatds separate, get 4 different cells
non identical
Kinetochores during Meiosis I
Same direction

during Mitosis and meiosis 2: separate sister chromatids

-Meiosis 1 separates maternal from paternal chromatid pairs
Genetic Diversity
Recombination: partial exchange of info between sister chromatids= unique combo of allels

Independent assortment: random segregation of chromatids to each gamete; unique combo of chromatids

BOTH DURING MEIOSIS 1