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82 Cards in this Set

  • Front
  • Back
M phase
division: mitosis
G1 phase
-prep phase btwn mitosis/dna replication
-checks for DNA damage
S phase
-genome replicated
G2 phase
-prep phase for mitosis, checks for completion of DNA replication
GO phase
-quiescent, not actively dividing
G1 restriction point
-montiors cell size, envmt conditions, interactions with neighbors
-commits to divide
G1 checkpoint
-stops cell cycle DNA damage detected
S phase checkpoint
-stops cell cycle DNA damage/stalled replication forks
G2/M checkpoint
-stops cell cycle unreplicated DNA/DNA damage
metaphase spindle assembly checkpoint
-delay separation of daughter chromatids until attched to mitotic spindle
CDKs
cyclin-dependent kinases
-pro that drives phases of cell cycle/transition
positive reg of Cdk
-phosphorylatins enhance activity
-dephosphorylation at inhib sites
-cyclin binding alters conformation and inc activity
negative reg of Cdk
-phosphorylation at inhib sites
-ubiquitin mediated destruction of cyclines
DNA Replication
where?
when?
-nucleus
-S-phase
euchromatin/heterochromatin
-euchromatin replicated early
-heterochromatin replicated late
Replication steps
-initiation
-elongation
-termination
helicase
-unwinds DNA at origin
DNA pol alpha
-primase
-synth RNA primers needed for synthesis
single strand DNA binding protein
stabilizes opening of double helix
DNA pol S
-bulk of DNA synth after RNA primers
-formation phosphodiester bonds
DNA topoisomerase
=gyrase
-relieves tension ahead of fork
DNA pol S
-proofreading activity
DNA ligase
-joins Okazaki fragments
Topoisomerase II
-cuts, reseals newly synth DNA molecules so they can separate
telomerase
-use RNA primer to generate special end structures (telomeres)
-functions as reverse transcriptase
DNA transcription
where?
when?
-nucleus
-high levels in G1, S, G2 phase
-euchromatin genes transcribed
core promoter
-region around transc start site
-includes TATA box (recruits RNA pol)
enhancers
-DNA sequences increase transcription
silencers
-DNA seq decrease transcription
cis-acting sequences
-enhancers, silencers, TATA box
-bind trans-acting pro
RNA Pol I
-transcribes rRNA genes
RNA Pol II
-transcribes mRNA and snRNA
RNA Pol III
-transcribes 5S rRNA and all tRNA
mRNA
-translated into peptide
rRNA
-used in building of ribosomes
-18S = small subunit
-28S,5.8S, 5S rRna = large subunit
tRNA
-carry AA to polypeptide
small nuclear RNA
-snRNA
-mediates processing of primary transcripts
capping
-add 7-methylguanosine-5'-triphosphate at 5' end
-protects from degredation
-regulates RNA export
-initiates ribosomal binding
polyadenylation
-add poly-a tail to 3'
-stabilization/nuclear export
splicing
-removal introns by spliceosome
-branch point A catalyzes
alternative splicing mRNA
-different patterns splicing = diff pro from same gene
genetic code
-triplet code (codons)
start codon
-AUG (methionine)
stop codon
-UGA
-UAA
-UAG
initiation complex
-tRNA w/methionine
-initiator AUG codon
proteasomes
-in nucleus
-degrade uneeded/damaged pro
ubiquitin
-tag pro for degredation
DNA binding structural motifs
-helix-loop-helix, leucine zipper, zinc finger, steroid hormone receptor motif
DNA methylation
-inhibits transctiption
nucleosome remodeling complexes
-move nucleosomes
-help transc factors find binding sites
histone modifications
-influence chromatin compaction
histone deacetylase
-remove acetyl groups
-favors compaction
histone acetylase
-chromatin more accessible
XIST gene
-X inactivation
microRNA
-block expression of other genes
antisense RNA
-binds to mRNA, physically blocks translation
smal interfering RNA
-interfere with expression of specific gene
single-stranded binding proteins
-bind to separated ssDNA to prevent annealing back together
transcription termination
-palindrome
-poly u sequence
fibroblast vs. fibrocyte
-fibroblast: proliferative capable of mitosis
-fibrocyte: fully differentiated, slowed metabolism
fibroblast: function?
-synthesize/secret ALL ECM components
nonactivated mast cells
-granules storing histamine, proteases, proteoglycans
activated mast cells
-release histamine, proteases, proteoglycans
-synth mediators from arichidonic acid
macrophage
-antigen presenting, phagocytic
-lots of signaling
collagen
-triple stranded
-characteristic, repeating structure
reticulin fiber
-support fo lymphoid tissue/liver
-made of type III collagen
-network: fluid/lymph pass through
elastic fibers
-made of proelastin, microfibril-assoc glycoprotein, fibrillin 1/2
fibrillin 1
-force-bearing structural suport
fibrillin 2
-regulates assembly
elastic fibers
-add resiliency to connective tissue
glycoaminoglycans
-polysach. side chains of proteoglycans
-polysach. of linear repeat disach. units
proteoglycans
-any pro w/one + covalently attached glycosaminoglycan chains
-very hydrated
proteoglycan: structure?
-axial hyaluronan molecule
-pro attatched by linker pro
-glycosaminoglycans attch to core pro
fibronectin
-binds integrins, collagen, proteoglycans
-helps cells attach to ECM
laminin
-bind collagen fibers via pelecan and entactin, and cell integrins
dense regular connective tissue: location? structure?
-in tendons and ligaments
-reg. oriented parallel bundles collagen
dense irregular connective tissue: location? structure?
-dermis of skin, submucose digestive tube
-fibroblasts sparse
loose connective tissue
-abundant e fibers and collagen bundles
proto-oncogene
-normal form of oncogene
oncogene
-cell affected by CA
characteristics of CA cells
-reduce dep. on signal from other cells
-less prone to apoptosis
-proliferate indefinitely
-unstable w/high mutation rate
-invasive, lack adhesion
-survive/proliferate foreign tissues
accumulation of mutations
-why CA is old age disease often