Unit 6 - DNA Replication, Transciption, Translation Flashcards

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1
Q

Topoisomerase

A

Uncoils the DNA

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2
Q

DNA Helicase

A

Breaks the H-bonds

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3
Q

DNA Polymerase III

A

adds nucleoside triphosphates

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4
Q

DNA Polymerase I

A

replaces RNA primers with DNA

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5
Q

Ligase

A

cleanse up and joins the okazaki fragments

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6
Q

Exonuclease

A

proofreader

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7
Q

Endonuclease

A

cleaves the bad parts

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8
Q

Transcription in Eukaryotes

A

Initiation: promoter region (TATA box); transcription factors help RNA polymerase bind

Elongation occurs

Termination: Polyadenylation Signal Sequence (AAUAAA) releases the pre-mRNA; post-transcription modifications (5’cap, poly-A tail, splicing [splicisomes; alternative splicing increases variation])

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9
Q

Transcription in Prokaryotes

A

Initiation: RNA polymerase directly binds to the promoter region

Elongation: translation happens simultaneously

Termination: termination sequence; no modifications

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10
Q

Termination in Eukaryotes

A

Initiation: universal start codon AUG

Elongation: tRNA brings specific animo acids based off the codons that match with the anticodon on the tRNA; peptide bonds form to make a polypeptide chain; translocation moving from right to left (EPA)

Termination: stop codon at A site

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11
Q

Acetylation

A

loosens/opens up the DNA; increases transcription; on HISTONES

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12
Q

Methylation

A

closes/condenses DNA; reduces/stops transcription; on nucleotide/DNA

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13
Q

Epigenetics

A

external to DNA that will regulate gene expression (heritable)

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14
Q

Retrovirus

A

transcription/translation from RNA to DNA

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15
Q

DNA point mutations/substitution mutations

A

Silent: no impact
Missense: depends on the R-group and if the function is still the same there will be no impact
Nonsense: nonfunctional protein is made

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16
Q

Frameshift

A

nucleotide base is added/deleted which will case all RNA after to shift

could code for accidental stop codon

after the shift point all codons could be different

17
Q

Eukaryotic Enhancers

A

Enhancers on a DNA sequence will activate transcription factors after folding over due to a bending protein; transcription factors can be activators or repressors

Help regulate gene expression

ex: Cytoplasmic Determinants and Induction

18
Q

HOX Genes

A

different sports for different genes

different body parts/characteristics will show depending on where it’s turned on

19
Q

TRP Operon (tryptophan)

A

repressive–normally ON; a substance causes it to be stopped

build up of tryptophan (in this case is also a corepressor which is an enzyme that is produced that also turns it off) will bind to the operator as a repressor (operator inhibits the operon) and the gene will not be produced

when tryptophan is removed, the operon will be able to function again

20
Q

LAC Operon (Lactose)

A

inducible–normally OFF; a substance causes it to start

takes advantage of lactose when it shows up for ATP

when there is lactose in the environment, an inducer will attach to the operator and the repressor is released which will allow the rest of it to make genes that break down the lactose and use it

21
Q

Lytic Cycle – bacteriophage

A
  1. insert virus DNA into bacteria
  2. break host DNA
  3. reproduce
  4. cell lysis
  5. infect other bacteria
22
Q

Lysogenic

A

viral DNA – replicated with binary fission

23
Q

Transformation

A
  • bacteria dies and the DNA is released into the environment
  • other bacteria uptake the naked DNA to change the geno/phenotype
24
Q

Transduction

A

cell to new, bacteria to bacteria

cell breaks and sends new DNA (virus) out

can also be bacteria DNA

25
Q

Conjugation

A

temporary bridge; passing plasmid

26
Q

Transposon

A

section of DNA (transposon) can be put into different section

27
Q

Restriction enzyme

A

recognize specific sequences on DNA (restriction sites)

28
Q

DNA Cloning

A
  1. cuts parts – corresponding/complementary sticky ends
  2. ligase binds phosphodiester linkage
  3. bacteria takes up and transforms (makes more)
    - scientists add antibody resistance on plasmid; all that’s left will be resistant plasmids (success)
29
Q

Gel Electrophoresis

A

cute DNA with restrictors
DNA = negative charge (will separate)
DNA Ladder: # of bases

top - large - negative
bottom - small - positive

30
Q

Polymerase chain reaction

A
  1. denaturation: add head to the separate strands
  2. annealing: cool down, add primers
  3. DNA synthesis (warmer) start

for electrophoresis and diagnostics