Manipulating genomes Flashcards
1
Q
DNA profiling
A
- PCR
- electrophoresis
- fluorescent tags
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
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
4
Q
Fluorescent tags
A
- mean that the DNA is visible under the UV light
- forms the DNA profile
5
Q
Uses of DNA profiling
A
- forensics
- disease risk
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
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
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
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
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
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
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
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
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
15
Q
Genetic engineering
A
- isolation of genes and suitable vectors
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
Negative of using pathogens for research
- 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
Patents
- 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
Somatic gene therapy
- 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
Germ line gene therapy
- 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)