6 Genetic modification Flashcards
What is a gene?
It is a section of a molecule of DNA that
codes for the production of a protein.
What does the coding strand of the DNA contain?
It contains triplets of bases.
What does each triplet code for?
Each triplet coding for one amino acid.
Why do different genes produce different proteins?
Different genes produce different proteins because each has a unique sequence of bases that codes for a unique sequence of amino acids.
What is an image that shows the role of DNA in protein synthesis?
What are examples for what the proteins that are produced can be?
- An enzyme that controls a particular reaction inside a cell or in the digestive
system. - A structural protein like keratin in hair, collagen in skin or one of the many
proteins found in the membranes of cells. - A protein hormone such as insulin.
- A protein with a specific function such as haemoglobin or an antibody.
What is the basis of genetic engineering?
The production of recombinant DNA.
What is recombinant DNA?
DNA made by genetic engineering,
by combining DNA from two species of organisms.
How is DNA combined from two species of organisms?
A section of DNA – a gene – is cut out of the DNA of one species and inserted into the DNA of another.
Why is this DNA called recombinant?
This is because the DNA from two different organisms has been ‘recombined’.
What is the organism that receives the gene from a different species called?
A transgenic organism.
What is a transgenic organism?
An organism that has been engineered with a gene from another species.
What happens to the organism receiving the new gene?
The organism receiving the new gene now has an added capability.
Why will it have an added capability?
It will manufacture the protein that the new gene codes for.
What is an example of the new organism manufacturing the protein that the new gene coded for?
A bacterium receiving the human gene that codes for insulin production will
make human insulin.
What happens if these transgenic bacteria are cultured by the billion in a fermenter?
They become a factory for making human insulin.
when did the breakthrough in being able to transfer DNA from cell to cell come about?
When it was found that bacteria have two sorts of DNA.
What are the two types of DNA that bacteria have?
The DNA found in their bacterial ‘chromosome’ and much smaller circular pieces of DNA called plasmids.
What is a plasmid?
It is a small circular piece of DNA found in bacteria and used in genetic engineering.
What do bacteria naturally do in terms of plasmids?
Bacteria naturally ‘swap’ plasmids.
What did biologists find out in terms of these plasmids?
Biologists found ways of transferring
plasmids from one bacterium to another.
What were biologists missing?
The next stage was to find molecular
‘scissors’ and a molecular ‘glue’ that could cut out genes from one molecule
of DNA and stick them back into another.
What are the molecular ‘scissors’ in question?
Restriction endonucleases/enzymes.
What are these restriction endonucleases/enzymes?
It is an enzyme used in genetic engineering to cut out a section from a molecule of DNA.
What are these restriction endonucleases/enzymes used for?
They are enzymes that cut DNA molecules at specific points. Different restriction enzymes cut DNA at different places. They can be used to cut out specific genes from a molecule of DNA.
What are ligases?
They are enzymes used to join pieces of DNA in genetic engineering.
What are ligases used for?
(or DNA ligases) are enzymes that join the cut ends of DNA molecules.
What does each restriction enzyme recognise?
Each restriction enzyme recognises a certain base sequence in a DNA strand.
What happens whenever restriction enzymes recognise a certain base sequence?
Wherever it encounters that sequence, it will cut the DNA molecule.
What can we suppose?
Suppose a restriction enzyme recognises the base sequence G-A-A-T-T-C.
How will the restriction enzyme then cut this sequence?
It will only cut the DNA molecule if it can ‘see’ the base sequence on both strands.
What are two ways in which restriction enzymes can cut DNA?
- Straight cuts.
- Staggered cuts.
What do restriction enzymes that make straight cuts produce?
Some restriction enzymes make a straight cut and the fragments of DNA
they produce are said to have ‘blunt ends’.
What do other restriction enzymes that make staggered cuts produce?
These produce fragments of DNA with
overlapping ends with complementary bases.
What are these overlapping ends called?
‘Sticky ends’.
Why are they called sticky ends?
This is because fragments of DNA with exposed bases are more easily joined by ligase enzymes.
What is a diagram which shows how restriction enzymes cut DNA to form blunt ends?
What is a diagram which shows how restriction enzymes cut DNA to form sticky ends?
What did this process allow biologists to do?
Biologists now had a method of transferring a gene from any cell into a
bacterium.
What could they now do in terms of plasmids and bacterium?
They could insert the gene into a plasmid and then transfer the plasmid into a bacterium.
What is this plasmid called?
A vector.
What is a vector?
Structure which can be used to transfer genes in genetic engineering, e.g. a plasmid.
What is a diagram which shows the stages in producing transgenic bacterium?