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79 Cards in this Set
- Front
- Back
2 functions of DNA polymerase
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5' -> 3' polymerase
3' --> 5' exonuclease |
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how often does DNA polymerase make a mistake?
with DNA mismatch repairrepair? |
1 in 10^7
1 in 10^9 |
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DNA polymerase can only join a nt to a _______ of a base associated with a double helix
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3'-OH
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makes short stretch of RNA using DNA as template
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DNA primase
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primers are removed by _____
gaps filled in DNA during replication by _______________ completed fragments joined by _________ |
nuclease
DNA repair polymerase DNA ligase |
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connects okazaki fragments
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DNA ligase
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adds additional nt repeats at the end of the chromosome
in what direction? |
telomerase
5'-->3' |
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somatic cell mutation aka _______ contributes to ____ of deaths in europe and north america
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cancer 30% of deaths
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DNA damage- releases G and A from DNA
phosphodiester backbone maintained |
depurination
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DNA damage- spontaneous loss of amino group from cytosine
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deamination
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DNA damage- caused by radiation, covalent linkage between two adjacent pyrimidines
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thymine dimers
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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 |
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way to spread favorable alleles and eliminate unfavorable
where and when does homologous occur? |
DNA recombination-
homologous region during meiosis prophase 1 |
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characteristics of mobile genetic elements
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- 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 |
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the enzyme that mediates the movement of the mobile genetic element it resides in
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transposase
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2 mechanisms by which transposons move
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cut and paste (non-replicative)
replicative |
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in what organisms are retro-transposons found?
what do they require? |
eukaryotes
reverse transcriptase (RNA dependent- DNA polymerase) |
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disease that involves an L-1 retrotransposon inserting into gene encoding Factor VIII
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hemophilia
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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 |
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DNA has an OH group at this C
H at this C |
OH at 3'
H at 2' |
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enzyme that carries out transcription
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RNA polymerase
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which is shorter- DNA or RNA?
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RNA
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how fast is transcription? can it repair its mistakes?
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40 nt/sec
cannot correct mistakes |
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mistake rate in RNA polymerase
does it need a primer? |
1 in 10^4
can start without a primer |
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components of prokaryotic transcription
how does it know where to start? |
RNA plymerase/ sigma factor
promoters: -35 and -10 start signals |
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primarily respoinsible for recognizing promoter sequence on DNA in prokaryotes
how long does it stay attached? |
sigma factor
first 10 nts |
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terminator for prokaryotic transcription
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stop signal of repeated Ts
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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 |
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RNA in prokaryotes mono or polycistronic? eukaroytes?
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prok: polycistronic
euk: monocistronic |
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RNA in eukaryotes is transcribed ________ and translated in _________
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the nucleus
cytoplasm |
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RNA capping happens at the ___ end and consists of what
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5' end
guanine NT with methyl group after production of ~25 nts |
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polyadenylation happens at the ____ end of the transcript
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3' end
trimming of end of transcript by enzyme that recognizes particular sequence then addition of AAA stretch by another enzyme |
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4 purposes of RNA modification in euks
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- 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 |
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is eukaryotic transcript colinear? prok?
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not colinear
prok is |
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splices intron sequences out
occurs after: |
snRNP complexes (small nuclear ribonucleoproteins)
after capping |
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% of genes that undergo alternative splicing
why is it favorable |
60%
makes genetic recombination between exons of different genes more likely |
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if the anticodon of tRNA is 5'-ACG-3' then what is its corresponding codon on mRNA
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3' - UGC- 5'
5' -CGU- 3' |
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the machinery of translation
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mRNA
tRNA ribosomes AAs aminoacyl tRNA synthetases protein factors ATP and GTP |
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small subunit of ribosome does what?
large subunit function? |
matches tRNA to codon on mRNA
links aa by peptide bonds |
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size of eukaryotic ribosome
prok? |
80s (40 and 60S)
70 (30 and 50S) |
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antibiotic that blocks binding of aminoacytl-tRNA to A-site of riosome (step 1)
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tetracycline
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antibiotic that blocks peptidyl transferase reaction on ribosomes (step 2)
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chloramphenicol (toxic- can cause aplastic anemia)
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antibiotic that blocks translocation reaction on ribosomes (step 3)
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erythromycin
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antibiotic that prevents transition from initiation complex to chain-elongating ribosome
causes miscoding |
streptomycin
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antibiotic that blocks initiation of RNA chains by binding to RNA polymerase
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rifamycin
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4 DNA-binding protein motifs
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helix-turn-helix
basic helix-loop-helix zinc finger leucine zipper |
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special class of HTH- regulatory proteins
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homeo-domain proteins (in proks and euks)
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makes up a helix-turn-helix
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two perpendicular alpha helices joined by a short strand of AAs
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makes up a basic helix-loop-helix
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two alpha-helices containing basic AAs linked by a loop (usually dimers)
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zinc fingers are made up of these two AAs bound by zinc to cause the protein to pucker
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cysteine and histidine units
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how far away are each DNA binding protein from one another?
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3.4nm aka 10bps aka 1 turn apart
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creates amphipathic area between its dimer
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leucine zipper
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where do DNA binding proteins bind?
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inverted palindromes
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how do repressors work?
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bind to operator
block RNA polymerase from binding to promoter |
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how do activators work?
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help initiate transcription by interacting with RNA polymerase, allowing it to bind to otherwise weak promoters
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the _____ the promoter is to the start site the stronger it is
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closer
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transcription is controlled by these 2 things
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DNA-binding proteins
regulatory sequences |
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site where transcription begins and
binding site for RNA polymerase |
promoter
|
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recognized by regulatory proteins and where is it?
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regulatory DNA sequences ~50 nts upstream
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tryptophan operon repressor can only bind if:
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bound to tryptophan
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tryptophan operon repressor falls off if:
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tryptophan concentration is low, operon is expressed to make tryptophan
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needed for CAP to be able to bind to DNA
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cAMP binding first
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when is cAMP present? what is the overall affect?
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when glucose is lower.
cAMP binds to CAP activator which can then bind to the operon, turning it on |
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situation in which the lac operon is turned on
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no glucose present (CAP bound)
lactose present (lac repressor off) |
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situations in which the lac operon is turned off
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in the presence of glucose (CAP won't bind)
in the absence of lactose (lac repressor is bound) no lactose to breakdown |
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where is the cap binding site?
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upstream of the RNA polymerase binding site (promoter)
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where are enhancer regions located? do they use energy?
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1000+ bp upstream. energy used to fold
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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 |
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rho-independent termination depends on this
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G-C rich palindrome that forms hairpin loop before stretch of U residues
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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
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ribosome binding site on RNA
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shine-dalgarno sequence (usually 4-7 nts 5' of the initiator AUG)
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protein binding at a hairpin before the start of translation does what?
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stops binding of translation components
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3 translational termination steps
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release factors recognize stop codons
causes addition of water molecule instead of aa polypeptide chain terminated |
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caused by Mutations of CBFA1
what is common? |
cleidocranial dysplasia
absent clavicle, late primary dentiton, supernumeray teeth |
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caused by Mutations of CBFA1
what is common? |
cleidocranial dysplasia
absent clavicle, late primary dentiton, supernumeray teeth |
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caused by mutations in the FGFR2 gene
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crouzon's
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caused by mutations in the FGFR2 gene
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crouzon's
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oligodontia is caused by defects in which genes?
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PAX9
MSX1 |
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oligodontia is caused by defects in which genes?
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PAX9
MSX1 |