DNA STRUCTURE AND REPLICATION Flashcards

1
Q

explain the central dogma of molecular biology

A

DNA–> RNA–> Protein.

It describes the flow of biological information between DNA/RNA/Protein.

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2
Q

what is the universal tree of life idea?

A

all life descended form one common ancestor / LUCA

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3
Q

what are the 3 domains of life?

A

Bacteria, Archaea, Eukarya.

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4
Q

Describe the similarities between 3 domains of life

A

bacteria and archaea have similar cellular architecture; archaea and eukarya have similar molecular architecture.

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5
Q

DNA nucleotides are made of?

A

base, sugar, triphosphate

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6
Q

what is a nucleoside?

A

base and sugar

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7
Q

dNTP

A

deoxyribonucleoside triphosphate (DNA)

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8
Q

NTP

A

ribonucleoside triphosphate (RNA)

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9
Q

what are purines?

A

adenine and guanine, 2 rings

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10
Q

what are pyrimidines?

A

cytosine, uracil and thymine

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11
Q

what is the general structure of DNA?

A

double stranded right handed helix with minor and major grooves, each strand runs antiparallel to the other

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12
Q

what are the rules / requirements for DNA replication?

A
  • DNA replication is semiconservative.
  • DNA polymerase synthesises DNA. needs a template strand
  • polymerisation only in 5’->3’
  • polymerisation needs dATP/CTP/GTP/TTP
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13
Q

Describe the process of strand separation?

A
  • DNA-A proteins binds and strands begin to separate
  • DNA-B protein (helicase) separates fork further. one on each strand, needs ATP.
  • strands are covered in single stranded binding proteins (SSBs), prevent reannealing.
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14
Q

Describe the process of DNA polymerisation?

A
  • lagging strand 5’–>3’
  • DNA polymerase polymerises leading strand continuously as it is complementary to DNA polymerase.
  • lagging strand replicated backwards through Okazaki mechanism. synthesis happens in small Okazaki fragments.
  • primers added by engaging with SSBs
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15
Q

E.coli DNA polymerase enzymatic functions?

A
  • 5’–> 3’ DNA polymerase activity = synthesising DNA
  • 5’–>3’ exonuclease activity = primer removal
  • 3’–>5’ exonuclease: proofreading. will cleave incorrect nucleotide and then DNApol will add correct one.
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16
Q

ddNTP

A

dideoxyribonucleotide triphosphate. chain terminating nucleotides; lack 3’ OH group needed for phosphodiester bond formation between 2 nucleotides

17
Q

What is needed for chain-termination method of DNA sequencing?

A

DNA single stranded template, DNA primer, DNA polymerase, dNTPS, ddNTPs

18
Q

describe the process of chain termination DNA sequencing?

A
  • DNA samples divided into 4 separate sequencing reactions; each has all 4 dNTPs and DNA polymerase. one ddNTP added to each. each ddNTP has a radioactive label
  • the formed fragments are separated by gel electrophoresis for each reaction so sequence can be ascertained
  • only useful for fragmented sequences <150bp
19
Q

how was sanger sequencing improved?

A

using separation on chromatographic columns and labelling the ddNTPs with fluorescent markers and having computer detect the wavelength when sequence is terminated. useful for fragments <500 BP.

20
Q

What is next generation sequencing? (illuminati)

A
  • large DNA molecules fragmented and ligated to short adaptors and attached to surface chambers
  • immobilises DNA with all 4 dNTPS
  • each has a specific fluorescent dye and terminator that has cleavable chemistry
  • one cycle = one nucleotide added = one colour generated
  • process repeated
  • computer analyses light produced
  • can sequence whole genomes
21
Q

what is PCR used for?

A

amplify a single copy or few copies of DNA

22
Q

stages of PCR?

A
  1. denaturation (95dc) = strands separate
  2. annealing (55dc) = primers base pair to complementary DNA template.
  3. extension (72dc) = polymerase extends from primer to form new DNA strand