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79 Cards in this Set

  • Front
  • Back
2 functions of DNA polymerase
5' -> 3' polymerase

3' --> 5' exonuclease
how often does DNA polymerase make a mistake?

with DNA mismatch repairrepair?
1 in 10^7

1 in 10^9
DNA polymerase can only join a nt to a _______ of a base associated with a double helix
3'-OH
makes short stretch of RNA using DNA as template
DNA primase
primers are removed by _____
gaps filled in DNA during replication by _______________
completed fragments joined by _________
nuclease

DNA repair polymerase

DNA ligase
connects okazaki fragments
DNA ligase
adds additional nt repeats at the end of the chromosome

in what direction?
telomerase
5'-->3'
somatic cell mutation aka _______ contributes to ____ of deaths in europe and north america
cancer 30% of deaths
DNA damage- releases G and A from DNA
phosphodiester backbone maintained
depurination
DNA damage- spontaneous loss of amino group from cytosine
deamination
DNA damage- caused by radiation, covalent linkage between two adjacent pyrimidines
thymine dimers
happens if deamination goes uncorrected

depurination

thymine dimers
substitution of one base for another

deletion of nt/base pair
incorrect nt places at site of deletion by G-T pairing

stall DNA replication machinery at site of damage
way to spread favorable alleles and eliminate unfavorable

where and when does homologous occur?
DNA recombination-

homologous region
during meiosis prophase 1
characteristics of mobile genetic elements
- in most organisms
- short sequences of DNA
- site specific recombination
- may be considered parasitic DNA
- generate genetic variation
- encode enzyme that mediates its movement
- may act as a mutagen
the enzyme that mediates the movement of the mobile genetic element it resides in
transposase
2 mechanisms by which transposons move
cut and paste (non-replicative)
replicative
in what organisms are retro-transposons found?

what do they require?
eukaryotes

reverse transcriptase (RNA dependent- DNA polymerase)
disease that involves an L-1 retrotransposon inserting into gene encoding Factor VIII
hemophilia
RNA type:

proteins coding

form the core of ribosome and catalyze proteins synth

regualte gene expression

serve as mRNA/ AA adaptors

used in RNA splicing, telomere maintenance, etc
mRNA

rRNAs

miRNA

tRNA

other small RNAs
DNA has an OH group at this C

H at this C
OH at 3'

H at 2'
enzyme that carries out transcription
RNA polymerase
which is shorter- DNA or RNA?
RNA
how fast is transcription? can it repair its mistakes?
40 nt/sec
cannot correct mistakes
mistake rate in RNA polymerase

does it need a primer?
1 in 10^4

can start without a primer
components of prokaryotic transcription

how does it know where to start?
RNA plymerase/ sigma factor
promoters: -35 and -10 start signals
primarily respoinsible for recognizing promoter sequence on DNA in prokaryotes

how long does it stay attached?
sigma factor

first 10 nts
terminator for prokaryotic transcription
stop signal of repeated Ts
what the 3 RNA polymerases in eukaryotes transcribe

I
II
II
I: most rRNA genes
II: protein-coding genes, miRNA genes, smoe small RNAs

III: tRNA genes, 5s rRNA gene, genes for other small RNAs
RNA in prokaryotes mono or polycistronic? eukaroytes?
prok: polycistronic
euk: monocistronic
RNA in eukaryotes is transcribed ________ and translated in _________
the nucleus

cytoplasm
RNA capping happens at the ___ end and consists of what
5' end

guanine NT with methyl group
after production of ~25 nts
polyadenylation happens at the ____ end of the transcript
3' end

trimming of end of transcript by enzyme that recognizes particular sequence
then addition of AAA stretch by another enzyme
4 purposes of RNA modification in euks
- increases stability
- aids in export to cytoplasm
- IDs molecule as mRNA
- used by the protein synthesis machinery to indicate that both ends of transcript are present
is eukaryotic transcript colinear? prok?
not colinear

prok is
splices intron sequences out

occurs after:
snRNP complexes (small nuclear ribonucleoproteins)

after capping
% of genes that undergo alternative splicing

why is it favorable
60%

makes genetic recombination between exons of different genes more likely
if the anticodon of tRNA is 5'-ACG-3' then what is its corresponding codon on mRNA
3' - UGC- 5'

5' -CGU- 3'
the machinery of translation
mRNA
tRNA
ribosomes
AAs
aminoacyl tRNA synthetases
protein factors
ATP and GTP
small subunit of ribosome does what?

large subunit function?
matches tRNA to codon on mRNA

links aa by peptide bonds
size of eukaryotic ribosome

prok?
80s (40 and 60S)

70 (30 and 50S)
antibiotic that blocks binding of aminoacytl-tRNA to A-site of riosome (step 1)
tetracycline
antibiotic that blocks peptidyl transferase reaction on ribosomes (step 2)
chloramphenicol (toxic- can cause aplastic anemia)
antibiotic that blocks translocation reaction on ribosomes (step 3)
erythromycin
antibiotic that prevents transition from initiation complex to chain-elongating ribosome
causes miscoding
streptomycin
antibiotic that blocks initiation of RNA chains by binding to RNA polymerase
rifamycin
4 DNA-binding protein motifs
helix-turn-helix

basic helix-loop-helix

zinc finger

leucine zipper
special class of HTH- regulatory proteins
homeo-domain proteins (in proks and euks)
makes up a helix-turn-helix
two perpendicular alpha helices joined by a short strand of AAs
makes up a basic helix-loop-helix
two alpha-helices containing basic AAs linked by a loop (usually dimers)
zinc fingers are made up of these two AAs bound by zinc to cause the protein to pucker
cysteine and histidine units
how far away are each DNA binding protein from one another?
3.4nm aka 10bps aka 1 turn apart
creates amphipathic area between its dimer
leucine zipper
where do DNA binding proteins bind?
inverted palindromes
how do repressors work?
bind to operator
block RNA polymerase from binding to promoter
how do activators work?
help initiate transcription by interacting with RNA polymerase, allowing it to bind to otherwise weak promoters
the _____ the promoter is to the start site the stronger it is
closer
transcription is controlled by these 2 things
DNA-binding proteins
regulatory sequences
site where transcription begins and
binding site for RNA polymerase
promoter
recognized by regulatory proteins and where is it?
regulatory DNA sequences ~50 nts upstream
tryptophan operon repressor can only bind if:
bound to tryptophan
tryptophan operon repressor falls off if:
tryptophan concentration is low, operon is expressed to make tryptophan
needed for CAP to be able to bind to DNA
cAMP binding first
when is cAMP present? what is the overall affect?
when glucose is lower.
cAMP binds to CAP activator which can then bind to the operon, turning it on
situation in which the lac operon is turned on
no glucose present (CAP bound)
lactose present (lac repressor off)
situations in which the lac operon is turned off
in the presence of glucose (CAP won't bind)

in the absence of lactose (lac repressor is bound) no lactose to breakdown
where is the cap binding site?
upstream of the RNA polymerase binding site (promoter)
where are enhancer regions located? do they use energy?
1000+ bp upstream. energy used to fold
there are multiple sigma factors for specific:

implications
promoters recognized

bacteria can make its own sigma factors that are specific for the promoters in its own genome
rho-independent termination depends on this
G-C rich palindrome that forms hairpin loop before stretch of U residues
how does rho-dependent termination work?

energy dependent?

what does rho function as?
Rho binds newly transcribed RNA, uses ATP to move, catches RNA polymerase stalled at termination site, breaks RNA_DNA-hybrid by working as a RNA_DNA helicase
ribosome binding site on RNA
shine-dalgarno sequence (usually 4-7 nts 5' of the initiator AUG)
protein binding at a hairpin before the start of translation does what?
stops binding of translation components
3 translational termination steps
release factors recognize stop codons
causes addition of water molecule instead of aa
polypeptide chain terminated
caused by Mutations of CBFA1

what is common?
cleidocranial dysplasia

absent clavicle, late primary dentiton, supernumeray teeth
caused by Mutations of CBFA1

what is common?
cleidocranial dysplasia

absent clavicle, late primary dentiton, supernumeray teeth
caused by mutations in the FGFR2 gene
crouzon's
caused by mutations in the FGFR2 gene
crouzon's
oligodontia is caused by defects in which genes?
PAX9
MSX1
oligodontia is caused by defects in which genes?
PAX9
MSX1