1. Technological Solutions

2. In 1977 Sanger et al. were able to work out the complete nucleotide sequence in a virus – (Phage 0X174) This breakthrough allowed researchers to use genome sequencing as a way of better understanding the genetics of living cells.

3. Work of Sanger relied on 3 important Developments Discovery of a way to break the DNA strand at specific sites Development of a process to copy or amplify the DNA strand Improvements in the methods for sorting and analyzing DNA Fragments.

4. Restiction Endonucleases As a means of Defending themselves against infection by foreign DNA most prokaryotes manufacture restriction endonucleases – Recognize specific short sequence of Nucleotides (target sequence) on a strand of DNA and cut the strand at a particular point within that sequence. – This point is the restriction site

5. Restriction Site

6. 2 Key Characteristics of Endonucleases make them useful Specificity – Cuts are specific and predictable. Same enzyme will cut the DNA Strand the same way each time. Producing an identical set of smaller pieces

7. Staggered Cuts – Most produce a staggered cut that leaves a few unpaired nucleotides remaining on a single strand at each end of the restriction fragment. Short sequences (Sticky Ends) can form base pairs with complementary sequences. Eg. Can form a base pair with another restriction fragment formed by the action of the same enzyme on a different strand of DNA. DNA Ligase will seal the gap in the new DNA Molecule creating Recombinant DNA by joining DNA from 2 Different sources

8. Recombinant DNA

9. DNA Amplification Process of generating a large sample of a Target DNA Sequence from a single gene or DNA fragment 2 Methods – Bacterial Vector – Polymerase Chain Reaction (PCR)

10. Bacterial Vector Relies on the action of Restriction Endonucleases When Target sample of DNA is treated with an endonuclease it is broken into a specific pattern of Restriction Fragments based on the enzyme specificity. Fragments are spliced into Bacterial Plasmids generating Recombinant DNA

11. First Recombinant created in 1973 by Cohen and Boyer Recombinant Plasmid can be returned to a bacterial cell. As Cell multiplies it replicates the plasmids. Plasmid serves as a cloning vector (a piece of DNA that can contain foreign DNA)

12. Plasmids in Bacteria

13. Creating Recombinant DNA

14. Figure 4.2 Bacterial Plasmid

15. Figure 4.3 Practical Uses of Plasmid Vectors

16. Figure 4.3 (1) Practical Uses of Plasmid Vectors

17. Figure 4.3 (2) Practical Uses of Plasmid Vectors

18. Figure 4.3 (3) Practical Uses of Plasmid Vectors

19. Figure 4.3 (4) Practical Uses of Plasmid Vectors

20. Viral Vectors Viruses can be used as an intermediary.

21. Figure 4.4 Practical Uses of Viral Vectors

22. Figure 4.4 (1) Practical Uses of Viral Vectors

23. Figure 4.4 (2) Practical Uses of Viral Vectors

24. Figure 4.4 (3) Practical Uses of Viral Vectors

25. Figure 4.4 (4) Practical Uses of Viral Vectors

26. Figure 4.4 (5) Practical Uses of Viral Vectors

27. Figure 4.4 (6) Practical Uses of Viral Vectors

28. Figure 4.4 (7) Practical Uses of Viral Vectors

29. Cloning a Gene in Bacteria Video

30. Polymerase Chain Reaction Practically an Automated method of replicating DNA that allows researchers to target and amplify a very specific sequence within a DNA Sample Relies on the action of DNA Polymerase.

31. Process of PCR Sample DNA Fragment is placed in a solution along with nucleotides and primers. Solution is heated to Break H Bonds between base pairs, causing Double Helix to open. Solution is cooled, Heat resistant DNA Polymerase is added and Replication begins. Cycle is repeated to generate large quantities of sequence in a short time for analysis

32. PCR Reaction

33. Sorting DNA Fragments Third Breakthrough that made Sanger’s Work possible was the development of Gel Electrophoresis Used to separate Molecules according to their mass and electrical charge. Process allows DNA Fragments to be separated so that they can be analyzed

34. Process Solution containing DNA Fragments is applied at one end of a gel. Electric current then applied which causes end of the gel to become polarized. As DNA is acidic it has a negative charge so the DNA will move towards the positive end. Smaller fragments move more quickly. After a period of time they separate into bands creating a DNA Fingerprint. Process refined to the point that Fragments can be separated if they differ by as little as a single nucleotide.

35. Gel Electrophoresis

36. DNA Fingerprint DNA Fingerprints