21.4 Genetic engineering Flashcards

(34 cards)

1
Q

what is genetic engineering?

A

the manipulation of the genome

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2
Q

basic outline of genetic engineering

A

desirable gene is isolated and then placed in another organism using a suitanle vector

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3
Q

what is an organism which carries a gene from another organism called?

A

transgenic
a genetically modified organism

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4
Q

what enzymes are used for isolating the desired gene?

A

restriction endonucleases

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5
Q

what is a sticky end?

A

a few bases left behind when the restriction endonucleases cuts the desired gene out

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6
Q

why are sticky ends useful?

A

makes it easier to insert a desired gene into the DNA of another organism

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7
Q

what are the two techniques for isolating a gene?

A

use of restriction endonucleases
use of reverse transcriptase

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8
Q

how is reverse transcriptase used to remove a desired gene?

A

used to produce a single strand of complimentary DNA from mRNA

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9
Q

why is the use of reverse transcriptase an advantage?

A

it makes it easier to identify the desired gene as the mRNA produced will be very different to the desired gene isolated by reverse transcriptase

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10
Q

what is the isolated DNA inserted into to be able to reach a host cell?

A

a vector

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11
Q

what is the most common vector used in genetic engineering?

A

bacterial plasmids

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12
Q

why are bacterial plasmids the preffered vector?

A

they are small
they can replicate independently

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13
Q

what is recombiant DNA?

A

when the plasmid goes into a new host cell and combines with the host’s DNA

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14
Q

what do plasmids used for vectors contain?

A

marker genes

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15
Q

what is an example of a marker gene?

A

one which gives antibiotic resistance
the bacteria is grown in a media containing antibiotic
checks that the bacteria has taken up the plasmid

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16
Q

what is used to cut open the plasmid?

A

the same restriction endonuclease used to isolate the desired gene

17
Q

why is it important that the plasmid is cut using the same restriction endonuclease?

A

it ensures that the sticky ends formed in the plasmid are complimentary to the bases in the desired gene

18
Q

how is the desired gene connected to the rest of the DNA in a plasmid?

A

DNA ligase forms phosphodiester bonds between the sugar and phosphate groups which joins the strands together

19
Q

what is the second gene marker in a plasmid used for?

A

to show whether a plasmid contains the recombinant gene

20
Q

how does the second gene marker activated?

A

if the DNA marker is inserted then the marker gene does not function

21
Q

what is transformation?

A

the process of transferring the plasmid containing the recombinant DNA into the host cell

22
Q

what are the methods of transformation?

A
  • permeable membranes
  • electroporation
23
Q

how are permeable membranes used for transformation?

A

the plasmid is placed in a calcium rich medium and high temperature in which the bacterial membrane to become more permeable to allow plasmids to enter

24
Q

what is electroporation?

A

when a small electric current is applied to the bacteria and the membrane becomes more porous to allow the plasmid to enter the cell

25
why is electroporation less useful in whole organisms?
the electric current can cause the membrane to become damaged and destroys the cell
26
what is electrofusion?
when a tiny electric is applied to the membranes of two cells which causes the cells to fuse and form a hybrid cell
27
what does the hybrid cell formed from electrofusion contain?
the DNA from both fused cells
28
why is electrofusion difficult in animal cells?
they are more difficult to fuse
29
how is electrofusion used to produce monoclonal antibodies?
when a tumour cell is fused with an antibody forms a hybridoma allows it to rapidly divide
30
what is a transformed cell?
a cell which has taken up a vector containing the desired gene
31
what are prokaryotes used in genetic engineering for?
bacteria have been genetically modified to produce: - insulin - clotting factors - antibiotics - vaccines
32
how are plants genetically modified?
a desired gene is placed in a plasmid with a marker gene then carried to the plant cell DNA callus forms which can each grow into a new plant
33
diagram for genetic engineering in plasmid
34
diagram for genetic engineering with a plant