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  • Hi. It's Mr. Andersen and in this podcast I'm going to talk about DNA fingerprinting.

  • We sometimes refer to this as DNA profiling or your genetic fingerprint. And basically

  • it started with this guy Alec Jeffries. Basically in his lab he was working with x-ray and looking

  • at DNA and what he figured out is he could tell a lot about a person by looking at their

  • DNA quote, unquote, fingerprint. In other words he could see who they were related to

  • and who they weren't. He could tell paternity for example. And so he was working at the

  • University of Leicester and basically figured out this whole idea of DNA fingerprinting.

  • This was around 1984. And basically for the next three years all DNA fingerprinting on

  • the planet went through this university. And so eventually it was privatized and this was

  • everywhere. And it will probably eventually be replaced by just DNA sequencing, sequencing

  • all the letters in DNA. But to make it understandable essentially what we have in a human is we

  • have long linear segments of DNA. But within that we have these genes. And so 99.9% of

  • our DNA in everyone is going to be exactly the same. The genes are going to be the same

  • but again you're going to have different copies or alleles of those genes. That's what makes

  • you, you. But if we look into this area in the middle, we used to call this junk DNA

  • but now we know it's really important in controlling gene expression we find that there's quite

  • a bit of variability in here, which shouldn't surprise us because this, the gene, makes

  • the protein and the protein makes the phenotype and that's really what natural selection is

  • selecting for or against. But this in the middle can go crazy. And so it does. And so

  • an example of one that we use in DNA fingerprinting is something called short tandem repeats.

  • Originally we started with something called VNTR, variable number tandem repeats and you'll

  • find in DNA sequencing that you have all kinds. So we had STRs we have VNTRs. Before that

  • we had restriction fragment length polymorphisms and so there's a bunch of different things

  • that we could look at. But we've kind of moved to this idea of these short tandem repeats.

  • They work great. There's quite a bit of variability in individuals. And so what is it? You basically

  • have letters of DNA that repeat over and over and over and over and over and over and over

  • and over. So sometimes, fifty times it repeats. And so what does that look like? Well if we

  • have these three individuals, we'll call this Mr. Blonde, Mrs. Red and then Mr. Mustache,

  • and so if we look at these three people their genes are going to be the same, but these

  • STRs are going to be different. These single or short tandem repeats are going to be different.

  • You can see that Mr. Blonde has more than Mr. Mustache and less than Mrs. Red. And so

  • if I make that a little bit easier to grasp onto, if I count them out and then remove

  • everything else, what we get is variability between all individuals. Everything else was

  • the same but we see variability in here. And we can cut these sections out using restriction

  • enzymes and them we can amplify them using polymerase chain reaction. And then we can

  • separate them using gel electrophoresis. So how does that work? Basically I'll take the

  • DNA and I'll put them in a little well. And so we're looking down on this. This is an

  • agarous gel. I could put Mrs. Red's and then Mr. Mustache, I could put those all in DNA.

  • Basically I would then turn on the voltage. So there's going to be a positive charge here

  • and a negative charge up here. DNA is a negative charge and so it's going to be pulled towards

  • the positive and so what's going to happen is those little fragments of DNA are going

  • to migrate. And so what does that allow me to do? It allows me to tell the difference

  • between each of these individuals. And so this is their fingerprint. But you can tell

  • this is a really bad fingerprint because we've got some, these two are exactly the same here

  • and so when they really do DNA profiling what they do is they generally us thirteen different

  • sections like this. And then those thirteen section are each going to be highly variable.

  • And so it's a good way to tell who's who. When would we ever want to do this? Forensics

  • is one reason and then also in paternity, figuring out who's dad. And so let's talk

  • about the murder. There was a murder that was committed Somebody was brutally murdered

  • by one of these three suspects, Mr. Blonde, Mrs. Red or Mr. Mustache. But they left blood

  • at the scene. And so what I can do is I can grab samples of DNA from each of our suspects

  • and then I could grab the blood itself and then I could do DNA fingerprinting on them.

  • So before we separate them you may think to yourself which of these looks guilty? Who

  • looks like they're capable of murder? And if we separate them then using that gel, what

  • we can see is that Mr. Blonde is guilty. In other words his blood matches up with the

  • crime scene. And so what do I mean by matching up? Well, those single or those short tandem

  • repeats, if we look horizontally are going to be exactly lined up. And if we were to

  • look at Mr. Blonde's son we'd find more similarities than we would between the others. And so basically

  • that's DNA profiling, DNA fingerprinting. It's much more sophisticated than that but

  • then again it's kind of on its way out. We'll eventually replace this with DNA sequencing.

  • In the US we, the FBI has started creating this database of DNA, which is a little scary.

  • And basically what they use are 13 different areas within the chromosome or the genome

  • and they they're looking at those short tandem repeats in there. Now why do I say that's

  • a little bit scary? I think you really want to protect your DNA because as we learn more

  • and more about genetics what's going to be found in your DNA, well predisposition to

  • Alzheimer's or breast cancer. Any of these things your insurance company would love to

  • get a hold of. And so it also doesn't answer the idea of Mr. Blonde, did he really do it?

  • Did the police frame him and contaminate the blood? So we don't know that. All it does

  • tell us is if we have two samples of DNA, the odds of two people having the same DNA

  • fingerprint are astronomical. Unless they're identical twins. And I hope that's helpful.

Hi. It's Mr. Andersen and in this podcast I'm going to talk about DNA fingerprinting.

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