1. DNA Restriction Analysis

2. DNA is Tightly Packaged into Chromosome s Which Reside in the Nucleus

3. Model of DNA DNA is Comprised of Four Base Pairs

5. 5’5’ 3’3’ Now, if all the elephants were the same, this would be a regular polymer. In DNA, one kind of SUPER POLYMER, there are four kind of elephants with the names: A, C, G, and T A CG T Note the backbone is the same for each one 5’5’ 3’3’

6. Deoxyribonucleic Acid (DNA)

7. DNA Schematic O CH 2 O P O O O Base CH 2 O P O O O Base OH Sugar O 5’ phosphate 3’ hydroxyl

8. 5’5’ 3’3’ Now, if all the elephants were the same, this would be a regular polymer. In DNA, one kind of SUPER POLYMER, there are four kind of elephants with the names: A, C, G, and T A CG T Note the backbone is the same for each one 5’5’ 3’3’

9. DNA Restriction Enzymes Evolved by bacteria to protect against viral DNA infection Endonucleases = cleave within DNA strands Over 3,000 known enzymes

10. Enzyme Site Recognition Each enzyme digests (cuts) DNA at a specific sequence = restriction site Enzymes recognize 4- or 6- base pair, palindromic sequences (eg GAATTC) Palindrone Restriction site Fragment 1 Fragment 2

11. 5 vs 3 Prime Overhang Generates 5 prime overhang Enzyme cuts

12. Common Restriction Enzymes EcoRI – Eschericha coli – 5 prime overhang Pstl – Providencia stuartii – 3 prime overhang

13. The DNA Digestion Reaction Restriction Buffer provides optimal conditions NaCI provides the correct ionic strength Tris-HCI provides the proper pH Mg 2+ is an enzyme co- factor

14. DNA Digestion Temperature Why incubate at 37°C? Body temperature is optimal for these and most other enzymes What happens if the temperature istoo hot or cool? Too hot = enzyme may be denatured (killed) Too cool = enzyme activity lowered, requiring longer digestion time

15. Agarose Electrophoresis Loading Electrical current carries negatively- charged DNA through gel towards positive (red) electrode Power Supply Buffer Dyes Agarose gel

16. Agarose Electrophoresis Running Agarose gel sieves DNA fragments according to size  Small fragments move farther than large fragments Power Supply Gel running

17. Analysis of Stained Gel Determine restriction fragment sizes Create standard curve using DNA marker Measure distance traveled by restriction fragments Determine size of DNA fragments Identify the related samples

18. Molecular Weight Determination Size (bp)Distance (mm) 23,00011.0 9,40013.0 6,50015.0 4,40018.0 2,30023.0 2,00024.0 Fingerprinting Standard Curve: Semi-log

19. NEB Cutter Predictions New England Biolabs Website to paste sequence and predict restriction enzyme sites and run a virtual gel to see what it would look like NEB Cutter