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Biotechnology – Gel Electrophoresis

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Presentation on theme: "Biotechnology – Gel Electrophoresis"— Presentation transcript:

1 Biotechnology – Gel Electrophoresis
How We Analyze DNA So That We Can Do Stuff With It.

2 A brave new world?

3 Biotechnology Manipulating genes to suit our purposes is nothing new.
Crossbreeding / Selective Breeding Picking organisms with traits you like and breeding them Goal is to get babies with traits that you REALLY like. Trouble is that Cross/Selective breeding is not terribly precise You may not get the results you want May recombine other traits in ways that were not intended, etc.

4 Biotechnology today Our tool kit… Genetic Engineering
Direct manipulation of DNA Allows much more specific control over particular genes Fewer unintended results However, if you are going to engineer DNA & genes & organisms, then you need a set of tools to work with this is a look at one of those tools… Our tool kit…

5 To manipulate DNA, we first need to be able to cut it up
WHY? Really it’s our only means of being able to analyze it Also, if we’re going to take certain parts that we like OUT of one organism’s DNA and stick them into another organism’s DNA, then we need to be able to “cut and paste” So how the heck can we cut up DNA?? Breaking out the scissors will NOT work. The answer is…. ENZYMES!

6  How do we cut DNA? Restriction enzymes restriction endonucleases
discovered in 1960s Occur naturally in bacteria Protect bacteria against viruses & other bacteria

7 So what do restriction enzymes do?
Do they just hack DNA up into bits? Well, sort of, but they only do it at certain, very predictable, locations along the DNA sequence The places where the restriction enzymes cut DNA are called restriction sites Specific sequences of “letters” on the DNA strand recognized by Restriction enzymes

8 Restriction enzymes Madam I’m Adam Action of enzyme
cut DNA at specific sequences restriction site Many different kinds of Restriction enzymes named after organism in which they are found CTGAATTCCG GACTTAAGGC CTG|AATTCCG GACTTAA|GGC

9 Many uses of restriction enzymes…
Now that we can cut DNA with restriction enzymes… Not only can we cut DNA out of the genome of one organism and stick it in another… Glow in the dark jellyfish gene inside of a mouse Human insulin gene inside of bacteria But we can also cut up DNA from different people… or different organisms… and compare it For what purpose? forensics medical diagnostics paternity evolutionary relationships and more…

10 How do we compare cut up DNA?
Compare DNA fragments by separating them according to SIZE. So, how do we separate DNA fragments according to size? We can’t see all the little pieces and pick them out with our fingers! run them through a “strainer” to sort them Gelatin is the strainer gel electrophoresis

11 “swimming through Jello”
Gel electrophoresis A method of separating DNA in a gelatin-like material using an electrical field DNA is negatively charged when it’s in an electrical field it moves toward the positive side DNA         + “swimming through Jello”

12 “swimming through Jello”
Gel electrophoresis DNA moves in an electrical field… so how does that help you compare DNA fragments? size of DNA fragment affects how far it travels small pieces travel more quickly through the gel large pieces travel slower & lag behind DNA        + “swimming through Jello”

13 DNA & restriction enzyme
Gel Electrophoresis DNA & restriction enzyme - wells longer fragments power source gel shorter fragments + completed gel

14 Different people have different DNA
Great…But how does the fact that different size pieces of DNA move at different speeds through a gel HELP us ANALYZE the DNA???? Gene 1 GCTTGTAACGGCCTCATCATCATTCGCCGGCCTACGCTT CGAACATTGCCGGAGTAGTAGTAAGCGGCCGGATGCGA repeats cut sites Cut the DNA GCTTGTAACG GCCTCATCATCATCGCCG GCCTACGCTT CGAACATTGCCG GAGTAGTAGTAGCGGCCG GATGCGA 1 2 3 DNA  + gene 1

15 Differences between people
Gene 1 cut sites cut sites GCTTGTAACGGCCTCATCATCATTCGCCGGCCTACGCTT CGAACATTGCCGGAGTAGTAGTAAGCGGCCGGATGCGA Gene 2 GCTTGTAACGGCCTCATCATCATCATCATCATCCGGCCT CGAACATTGCCGGAGTAGTAGTAGTAGTAGTAGGCCGG 1 2 3 DNA fingerprint DNA  + allele 1 allele 2

16 Uses: Evolutionary relationships
Comparing DNA samples from different organisms to measure evolutionary relationships turtle snake rat squirrel fruitfly 1 3 2 4 5 1 2 3 4 5 DNA +

17 Uses: Medical diagnostic (genetic testing)
Comparing normal allele to disease allele chromosome with normal gene 1 chromosome with disease-causing gene 2 Gene 1 Gene 2 DNA Example: genetic test for Huntington’s disease +

18 Uses: Forensics Comparing DNA sample from crime scene with suspects & victim suspects crime scene sample S1 S2 S3 V DNA +

19 DNA fingerprints Comparing blood samples on defendant’s clothing to determine if it belongs to victim DNA fingerprinting comparing DNA banding pattern between different individuals ~unique patterns

20 Electrophoresis use in forensics
Evidence from murder trial Do you think suspect is guilty? blood sample 1 from crime scene blood sample 2 from crime scene blood sample 3 from crime scene “standard” blood sample from suspect OJ Simpson blood sample from victim 1 N Brown blood sample from victim 2 R Goldman “standard”

21 Uses: Paternity Who’s the father? Mom F1 F2 child DNA +

22 I’m a-glow! Got any Questions?

23 In reality, much of each person’s DNA is identical to every other person…
Don’t want the genes for important proteins to be messed up, do we????? So How/Why is each person’s DNA pattern different? There are big sections of “junk” DNA within our genomes “Junk” DNA doesn’t code for proteins made up of repeated patterns CAT, GCC, and others each person may have different number of repeats Why are these repeated patterns there? Not entirely clear… many sites are found on our 23 chromosome pairs with different repeat patterns GCTTGTAACGGCCTCATCATCATTCGCCGGCCTACGCTT CGAACATTGCCGGAGTAGTAGTAAGCGGCCGGATGCGA GCTTGTAACGGCATCATCATCATCATCATCCGGCCTACG CGAACATTGCCGTAGTAGTAGTAGTAGTAGGCCGGATGC


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