DNA sequencing Flashcards

1
Q

describe dideoxy chain termination

A

aka Sanger sequencing
developed to sequence DNA in 1977
developed by Fred Sanger
very robust = low error rate, highly reliable

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2
Q

sequencing by ABI 3730

A

sample is prepared by dideoxy chain termination on large scale by robotics

read length of up to 900bp- 99.95% accuracy

handles 48 or 96 samples simultaneously

over 1000 samples per day

only performs separation of LABELLED dna

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3
Q

ABI 3730 automated DNA sequencing

A

used to sequence human genome
produced 23 thousand million bases of sequence
took 13 years
2.7 billion to complete

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4
Q

how does sequencing by dideoxy chain termination work?

A
  1. template
  2. enzymatic sequencing section (DNA polymerase makes multiple copies of DNA)
  3. size separation of products by capillary electrophoresis - sorting by size
  4. detection of reaction products (sequential detection of terminating nucleotide to identify the base)
  5. readout of sequence - reconstructing the sequence
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5
Q

similarity of PCR and dideoxy chain termination

A
  • some protocols cycle through repeated temperatures but only use a single forward primer

amplification is limited and not exponential

always uses a DNA polymerase

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6
Q

sequencing by dideoxy chain termination - the reaction

A
sequencing reaction
strand seperation
annealing primer
extension 
chain termination
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7
Q

describe sequencing using DNA polymerase

A
  • DNA is mixed with reaction components including dideoxy and dideoxy-nucleotides
  1. single strand oligonucleotide is bound to template
  2. polymerase recognises the DNA structure, then forms initation complex
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8
Q

describe requirements of DNA dependent DNA polymerase

A
  1. template strand that extends beyond a primer
  2. free 3’ OH group on primer
  3. all 4 deoxy nucleotide triphosphate
  4. Mg2+ ions
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9
Q

describe final step: chain termination requirements

A
  1. template strand extends a primer forming partial duplex
  2. free 3’ OH group on primer
  3. all 4 deoxy nucleotide triphosphates
  4. all 4 dideoxy nucleotide triphosphates
  5. mg2+ ions
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10
Q

what is DNA elongation terminated by

A

addition of dideoxynucleotide as it has position 3 OH group missing which prevents extension

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11
Q

describe sequencing using DNA polymerase

A
  1. polymerase commences elongation from 3’ terminus
  2. as enzyme encounters a particular nucleotide in sequence it picks out and incorporates complementary nucleotide into elongating strand
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12
Q

how do reaction products vary in length terminated by ddNTP

A
  • where ddCTP is incorporated = represents all positions in sequence where cytosine occurs
  • if all 4 dideoxy nucleotides are present in the reaction the population of molecules produced represent all possible positions in sequence from same point to end
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13
Q

describe size separation by gel electrophoresis

A
  • nucleic acid passes through gel matrix by applying a voltage across two electrodes
  • negatively charged nucleic acid migrates towards positive electrode
  • matrix retards molecule according to size
  • those larger are retarded to a greater extent and move through matrix more slowly
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14
Q

how is the sequence determined

A

sequence is determined by direct comparison of lengths of products terminated by each of the 4 dideoxy nucleotides

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15
Q

what does a measurement of fluorescence do

A

generates trace and base calling is automated

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16
Q

how is DNA sequencing by dideoxy chain termination routinely used

A

health = test for specific genetic mutations in patients with suspected genetic diseases

  • used to confirm all types of mutation
  • identifying HIV haplotypes resistant to anti-retrovirals to determine therapy haart
17
Q

how is DNA sequencing by dideoxy chain termination still used

A

mammalian and pathogen gene sequencing
clone or PCR amplicon sequencing to confirm clones sequence or site-directed mutagenesis
walking a gene to identify a causative mutation in gene studies
confirmation of causative variants associated with genetic disease following association study