Manipulating genomes Flashcards

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1
Q

DNA profiling

A
  • PCR
  • electrophoresis
  • fluorescent tags
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2
Q

PCR

A
  • at 95 degrees DNA fragment splits into 2 strands due to the complementary hydrogen bonds between baes
  • temperature is then reduced to 55 degrees and primers anneal to the strands
  • then temperature is raised to 72 degrees and free DNA nucleotides join to complementary base pairs
  • DNA polymerase seals up the phosphodiester bonds along the backbone
  • process is then repeated multiple times to produce identical DNA strands
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3
Q

Electrophoresis

A
  • cut DNA fragments need to be split up
  • fragments move towards the anode due to their negative charge
  • the smaller fragments will travel faster and further in a set time compared to larger fragments
  • the DNA fragments are then transferred onto a membrane by Southern Blotting
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4
Q

Fluorescent tags

A
  • mean that the DNA is visible under the UV light
  • forms the DNA profile
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5
Q

Uses of DNA profiling

A
  • forensics
  • disease risk
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6
Q

Disease Risk

A
  • identifying individuals who are at risk of developing particular diseases
  • specific gene markers can be identified and observed in DNA profiles
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7
Q

Forensics

A
  • PCR and DNA profiling is done on traces on DNA found at a crime scene
  • obtained from saliva, blood, hair
  • can then identify criminals
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8
Q

DNA sequencing (chain termination)

A
  • DNA is mixed with a primer, DNA polymerase, nucleotides and terminator bases
  • strands separate by breaking the hydrogen bonds and primers anneal to the strands
  • DNA polymerase starts to build new DNA strands by adding bases complementary to the original strand
  • when terminator base is incorporated no more bases can bind after it so the fragment shortens
  • repeated cycle to get DNA strands of various lengths
  • separated by gel electrophoresis
  • forms genome and can be analysed by scientists
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9
Q

Pyrosequencing

A
  • advances in gene technology
  • lead to faster mapping of genomes
  • light is produced when the correct base binds to the strand
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10
Q

Computational biology

A
  • uses data to build theoretical models
  • analysis of large amounts of data
  • helps identify genes linked to specific diseases in populations
  • see evolutionary relationships between organisms
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11
Q

Bioinformatics

A
  • development of the software and computing tools needed to organise and analysis raw biological data
  • make sense of enormous quantities of data
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12
Q

Epidemiology

A
  • sequencing human genomes to fin areas of specific genetic disease
  • sequence pathogens genomes
  • identify antibiotic resistant strains of bacteria
  • track the progression of an outbreak
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13
Q

Evolutionary relationships

A
  • DNA sequences of different organisms can be compared
  • how long ago two species diverged from a common ancestor
  • build evolutionary trees
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14
Q

Synthetic biology

A
  • ability to sequence the genome of organisms
  • understand how each sequence is translated into amino acids
  • new area of biology
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15
Q

Genetic engineering

A
  • isolation of genes and suitable vectors
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16
Q

Method of genetic engineering

A
  • select most desired gene
  • cut out the gene by using restriction enzymes to produce sticky ends
  • then insert recombinant DNA into a vector ( bacterial plasmid)
  • plasmid DNA is cut with the same restriction enzymes so both strands have complementary sticky ends
  • then transfer the vector into a host cell by electroporation
17
Q

Genetic manipulation ( insect resistant soya beans)

A
  • produce a toxic protein to pests tat eat the plant
  • resistant to the common weed killer
18
Q

Positives of manipulation ( soya beans)

A
  • increases the crop yield with less labour
  • less expensive
  • protects the environment
  • reduce the amount of pest spraying
19
Q

Negative of manipulation ( soya beans)

A
  • insects may become resistant to pesticides in GM crops
  • other species may become damaged in the process
20
Q

Pharming

A
  • production of human medicines
21
Q

Positives of pharming

A
  • drugs are made in lager quantities
  • more readily available
22
Q

Negatives of Pharming

A
  • harmful side effects for the animal
  • treating animals as assets to be treated how we chose
23
Q

Using pathogens for research

A
  • to find treatments for diseases
24
Q

Positive of using pathogens for research

A

could find cures for previously untreatable disease

25
Q

Negative of using pathogens for research

A
  • many become infected with the pathogen and cause an outbreak
  • GM pathogen may revert back and start an outbreak
  • if handled incorrectly then issues of biowarfare arise
26
Q

Patents

A
  • impact less developed areas and farmers
  • cant afford to buy the patent to sell on the crop
  • cant afford to repeatedly plant the crop
27
Q

Somatic gene therapy

A
  • uses body cells
  • replacing the mutant allele with healthy allele in the affected body cell
  • success in immune diseases, leukaemia’s and myelomas
  • temporary solution
  • pass the faulty gene onto offspring
28
Q

Germ line gene therapy

A
  • inserting the health allele into embryo straight after fertilisation
  • would pass on to offspring
  • illegal in human embryos
  • impacts are unknow
  • increase future implications ( cosmetic changes)