Post on 26-Dec-2015
Genetic engineering to produce an organism which will make a ‘foreign’ protein:
·Obtain ‘foreign’ gene·Amplify using PCR·Insert gene into a vector
Then either:
·(use a marker gene to identify transformed organisms)
·Collect the protein produced when the gene is expressed in the transformed organism
Or:
·Insert gene directly into target cells for gene therapy – the gene is expressed and the functional protein is produced.
Genetic engineering for analysis:
·Obtain the DNA – this could be a target gene or sample of DNA for forensic analysis.
·Amplify using PCR·Carry out electrophoresis – this could be for:
oGenetic fingerprintingoRestriction mappingoDNA sequencing – maybe to identify the presence of a particular gene when screening so genetic counselling can be offered.
By the end of the lesson you should be able to • Give some uses of genetic engineering.• Have an overview of genetic engineering.• Know how scientists obtain the DNA
fragments they are interested in and amplify them using PCR.
Genetic engineering to produce an organism which will make a ‘foreign’ protein:
·Obtain ‘foreign’ gene·Amplify using PCR·Insert gene into a vector
Then either:
·(use a marker gene to identify transformed organisms)
·Collect the protein produced when the gene is expressed in the transformed organism
Or:
·Insert gene directly into target cells for gene therapy – the gene is expressed and the functional protein is produced.
Genetic engineering for analysis:
·Obtain the DNA – this could be a target gene or sample of DNA for forensic analysis.
·Amplify using PCR·Carry out electrophoresis – this could be for:
oGenetic fingerprintingoRestriction mappingoDNA sequencing – maybe to identify the presence of a particular gene when screening so genetic counselling can be offered.
i.e. transferring the genes of one organism into another organism
What is a genome?
• The entire DNA sequence of an organism (i.e. all the DNA both coding and non-coding).
The Human Genome Project successfully mapped the human genome in 2003
i.e. transferring the genes of one organism into another organism
DNA Technology overview
1. Obtain the DNA fragment required – using reverse transcriptase or restriction endonuclease enzymes
2. Amplify the fragment using PCR3. Either:
Identify fragments using electrophoresis (for sequencing, mapping or genetic fingerprinting)
Or: Use fragments in gene therapy
Method 1 – Using reverse transcriptase:
• What is transcription?
• Therefore what do you think the enzyme reverse transcriptase does?
• As the DNA which is produced has complementary nucleotides to mRNA it is called complementary DNA or cDNA.
• We can use reverse transcriptase to produce cDNA for a particular gene from that gene’s mRNA.
• Read page 246 and 247 of the text book and make short notes on page 21 of your booklet.
1 virus = 2 minutes
Method 2 Using restriction endonuclease:
• The second way to isolate the gene you is done by an enzyme called a restriction endonuclease
• Each restriction endonuclease recognises a different DNA base sequence
• Restriction endonuclease enzymes.
E coli bacteriumEco R1 restriction enzyme
Think back to your work on protein structure (module 1). Why does each enzyme molecule recognise a different DNA base sequence?
The enzyme’s active site has a specific shape which is complimentary to the shape of a specific DNA base sequence.
Complete the question at the bottom of page 21 in your booklet now.
TCC GGACCG ACGTCGGT TCGAATCAGGCCTGG CTGCA GCCAAGCT TAG
Use a different colour to identify where each enzyme cuts.
(NB Eco R1 is not used – some of the others may not cut either)