DNA & RNA Flashcards

1
Q

3 components of DNA/RNA

A
  1. nitrogenous base
  2. ribose/deoxyribose
  3. at least 1 P group
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2
Q

nucleoside

A

nitrogenous base covalently linked to a 5-carbon sugar

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3
Q

nucleotide

A

nucleoside + P group

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4
Q

nucleoside triphosphates

A

ATP (adenosine triphosphate)

CTP

TTP

GTP

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5
Q

what happens when ATP is consumed in metabolic processes

A

converted to ADP or AMP

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6
Q

function of double helix in DNA

A

protection

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7
Q

GC rich sequences

A

higher thermal stability due to greater no. of H bonds

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8
Q

which nitrogenous base is different in RNA?

A

uracil (unmethylated form of thymine)

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9
Q

mRNA

A

carries genetic material from nucleus to ribosome

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10
Q

tRNA

A

delivers amino acids to ribosomes

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11
Q

rRNA

A

links amino acids to make protein

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12
Q

lagging strand

A

other direction

DNA polymerase can’t continuously synthesise strand - produce Okazaki fragments

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13
Q

Okazaki fragments

A

short segments of DNA each starting with primer

later join to form continuous strand

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14
Q

components of PCR

A
  1. DNA template (contains target region to amplify)
  2. DNA polymerase (heat-resistant)
  3. DNA primers (need 2 which are complementary to 3’ end of each strand of DNA)
  4. deoxynucleoside triphosphates (dNTPs) - building blocks for DNA polymerase to synthesise new strand
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15
Q

what solution does PCR take place in?

A

buffer solution

suitable for enzymes

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16
Q

PCR procedure

A
  1. Denaturation (96C)
    - denatures DNA strand to provide single-stranded template
  2. Annealing (55-65C)
    - primers bind to comp. sequences on single-stranded template
  3. Extension (72C)
    - DNA polymerase synthesises new DNA strand comp. to DNA strand after adding free comp. dNTPs from reaction mixture

+ REPEAT

17
Q

gel electrophoresis

A

checks whether PCR has been done correctly

separation of PCR products
- compared with DNA ladder = molecular weight marker

DNA visualised with stain under UV light

18
Q

advantages of PCR

A

simple

highly sensitive

produces millions of products

19
Q

disadvantages of PCR

A

prone to contamination (= false results)

requires information about target sequence to generate primers for selective amplification

DNA polymerases prone to error - can lead to mutations in sequences