B21 Flashcards

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1
Q

Bioinformatics

A

development of software and computing tools needed to analyse biological data
- develop algorithms, statistical tests, mathematical models to help understand
- studies generate data on DDNA sequences, protein sequences & relationship between genotype and phenotype

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2
Q

Computational biology

A
  • uses data from bioinformatics to build theoretical models of biological systems
  • the study of biology using computational techniques
  • analyse biodata
  • work out protein 3D structure
  • help understand pathways e.g. gene regulation
  • help identify genes linked to diseases etc.
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3
Q

DNA barcoding

A

Identify genome sections common to all species but varies between them & make comparisons
- Use cytochrome C oxidase

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4
Q

cytochrome C oxidase usage in DNA barcoding

A
  • in mitochondrial DNA
  • codes for respiration enzyme
  • small = quick & cheap sequencing
  • varies to give clear differences between species
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5
Q

Benefits of analysing genomes of pathogens

A

-fast & relatively cheap
- doctors find infection source
- doctors can identify antibiotic-resistant strands = prevent further resistance by only using antibiotic when needed
- track spread & transmission & plan suitable treatment
- track progress of an outbreak
- Identify useful regions in pathogen genome for developing new drugs & vaccines.

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6
Q

synthetic biology

A
  • Design and construction of artificial biological pathways
  • Redesign of existing biological systems
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7
Q

synthetic biology techniques

A

genetic engineering

biological systems used in industrial context e.g. immobilised enzymes

synthesis of new genes
- replace faulty ones

synthesis of whole new organism

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8
Q

synthetic biology techniques

A

genetic engineering

biological systems used in industrial context e.g. immobilised enzymes

synthesis of new genes
- replace faulty ones

synthesis of whole new organism

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9
Q

next-generation sequencing

A
  • uses flow cell (plastic slide) instead of gel or capillaries
  • millions of DNA fragments bind to slide & replicated in situ in PCR to form clusters of DNA fragments
  • clusters imaged and sequenced at same time = ‘massively parallel sequencing’
  • constantly being developed
  • very fast and efficient (human genome can be sequenced within days)
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10
Q

The two methods of isolating desired gene in genetics engineering

A

1) restriction nuclease enzymes
2) reverse transcriptase of mRNA –> cDNA

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11
Q

Why are plasmids used as vectors in genetic engineering?

A
  • small circular DNA
  • separate from chromosomal DNA & can replicate independently
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12
Q

DNA ligase

A

reforms phosphodiester bonds between sugar phosphate groups

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13
Q

Transferring the vector: electroporation and electrofusion

A

electroporation:
- small electric current applied to bacteria
- makes membrane porous, so plasmids enter
- but must control power otherwise could destroy cell

electrofusion:
- tiny electric currents applied to membranes of 2 diff cells
- fuses cells together, forming hybrid/polypoid cell containing DNA from both.

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14
Q

genetic engineering in plants

A
  • agrobacterium tumefaciens = bacterium that causes tumours in plants
  • a. tumefaciens & plant cell w/ desired gene undergo electrofusion:
  • cellulase removes cell wall
  • electrofusion forms polypoid cell
  • plant hormones stimulate growth of new cell wall
  • callus formation & production of many cloned, transgenic plants
  • plants transferred to soil to develop into fully differentiated adult plants
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15
Q

genetic engineering in animals

A
  • harder to manipulate animal cell membranes
  • virus = common vector in animals
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16
Q

DNA libraries

A
  • store a living record of the DNA of another organism.
  • Source of DNA fragments for further genetic engineering applications & further study of their functions
17
Q

ethical concerns of GM pathogens

A
  • could be used in biological warfare
  • made more virulent
  • made resistant to treatment
  • largely prohibited area of research as could be harmful to health & safety of the public
18
Q

Problems
with somatic cell gene therapy

A
  • somatic cells have limited life cycle
  • healthy allele passed on every time cell divides
  • BUT these cells are replaced from stem cells, which contain the faulty allele
  • Therefore, only temporary solution
  • A treated individual can still pass on the faulty allele.
19
Q

Germ line cell gene therapy

A
  • healthy allele inserted into germ cell (usually eggs) or the embryo immediately after fertilisation as part of IVF treatment
  • Individual would be born healthy with normal allele
20
Q

Germ line cell therapy concerns

A
  • ethical and medical
  • potential impact on individual is unknown
  • human rights of unborn individual violated
  • done without consent & irrevocable process
  • concerns of future usage enabling people to choose desirable or cosmetic characteristics of their offspring.