Recombinant DNA technology Flashcards

1
Q

What is the definition of recombinant DNA technologies?

A

Joining bits of DNA together (sometimes from different species). These are then inserted into an organism to produce (express) a useful protein.

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2
Q

What is an example of a gene used in recombinant DNA technologies?

A

Green fluorescent protein (GFP) (from jellyfish)

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3
Q

Describe the molecular structure and features of a plasmid (3)

A
  • Derived from endogenous DNA
  • Circular, double stranded
  • Replicate independently from host’s chromosomal
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4
Q

What are 4 key components of a plasmid?

A
  • Origin of replication (ORI)
  • Antibiotic resistance gene
  • Promoter
  • Restriction site
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5
Q

What is the role of the origin of replication?

A

allows initiation of replication using host DNA polymerase

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6
Q

What is the role of the antibiotic resistance gene?

A

allows selection of the cells which have take up the protein/plasmid (all others killed by antibiotic)

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7
Q

What is the role of the promotor?

A

Drives expression of your favourite gene (e.g. insulin or GFP) in cells with appropriate transcription factor machinery

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8
Q

What is the role of the restriction site?

A

so that you can put what you want into the backbone

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9
Q

What are 2 tools used for recombinant DNA technologies?

A
  1. Cutting and pasting DNA into plasmids
  2. Amplifying plasmids - transformation
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10
Q

What 2 things are used for cutting and pasting DNA into plasmids?

A

restriction enzymes and DNA ligase

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11
Q

What is the general function of restriction enzymes and where are they naturally found?

A

○ Naturally found in bacteria
○ Used to stop invading pathogens/phages entering the cells
= defence system to degrade foreign DNA

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12
Q

What do restriction enzymes do in terms of recombinant DNA technologies?

A

Cuts dsDNA at specific sequences
- Has to be double stranded and unmethylated (= from hosts)
- Cuts so that there’s overhang = sticky ends

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13
Q

What are sticky ends used for?

A

Add to what we want to insert to plasmid with corresponding sticky ends, then repair DNA

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14
Q

What does DNA ligase do in terms of recombinant DNA technologies?

A

Catalyses the formation of phosphodiester bond to repair nick in DNA backbone

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15
Q

What is transformation?

A

transfer of plasmids into bacteria

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16
Q

Which bacteria do we transform?

A

the bacteria selected by antibiotic resistance contained on plasmid

17
Q

What is the difference between using a plasmid with a bacterial gene vs with a eukaryotic gene when inserted into bacteria?

A

The gene will be expressed if bacterial, only replicated lots if eukaryotic

18
Q

What is the difference between prokaryotic and eukaryotic genes, and what does this mean for prokaryotes?

A

Prokaryotic genes don’t have introns, and thus prokaryotes don’t have the machinery to process eukaryotic introns

19
Q

What is the significance of having a universal genetic code?

A

• All organisms read the same codons as the same amino acids
.: we can transform a human gene into bacteria and it will still make the same protein

20
Q

To use prokaryotes to replicate a eukaryotic gene, which part(s) of the gene are used?

A

coding sequence only!

21
Q

When and why is it best to transform the plasmid into bacteria?

A
  • Bacteria are best if don’t need post-translational modification/folding
  • Fast and cost-effective
22
Q

If the protein of interest requires post-translational modification, what are the best cells to use?

A

Mammalian, transgenic

23
Q

what are examples of post-translational modification? (2)

A

cleaving C chain, glycosylation

24
Q

What cells are used to make EPO? Why?

A

CHO cells - very good at glycosylating proteins

25
Q

What protein is goat milk used to produced? What is its function?

A

anti-thrombin (AT) - Blocks the function of thrombin, which is in the clotting cascade

26
Q

How is AT produced?

A

milk specific promotor added to human AT gene (is a mammary cell specific protein so AT not produced in every cell for whole life). AT is then produced in the milk and purified out