DNA Replication (Updated)

Captions are on! Click CC at bottom right to turn off. DNA. We talk about it so much—it is the ultimate
director for cells and it codes for your traits. With a molecule that has a function like that,
it makes sense that when you make another cell—like in cell division—you would also
need to get more DNA into the new daughter cell. And that introduces our topic of DNA replication,
which means, making more DNA. First, let’s talk about where and when. First where—well if it’s in a eukaryotic
cell, it occurs in the nucleus. However, remember, not all cells have a nucleus. Such as prokaryotic cells. They don’t have a nucleus. Still both prokaryotic and eukaryotic cells
do DNA replicationm but there’s some differences between the two that this clip doesn’t go
into. Next, when. When does this happen? Well a cell is going to need to do this before
it divides so that the new daughter cell can also get a copy of DNA. To get specific, in a eukaryotic cell, that’s
going to be before mitosis or meiosis in a time known as interphase. I think DNA replication would actually make
a great video game. Still waiting for that to be invented. I’m going to introduce the key players in
DNA replication so that you can get some background information. Now, remember, these are just some major key
players. There’s a lot to this process. Many of the key players are enzymes. In biology, when you see something end in
–ase, you might want to check as it’s very possible that it’s an enzyme. Enzymes have the ability to speed up reactions
and build up or break down the items that they act on. So here we go with the key players. Helicase- the unzipping enzyme. If you recall that DNA has 2 strands, you
can think of helicase unzipping the two strands of DNA. Helicase doesn’t have a hard time doing
that. When unzipping, it breaks through the hydrogen
bonds that hold the DNA bases together. DNA Polymerase- the builder. This enzyme replicates DNA molecules to actually
build a new strand of DNA. Primase- The initializer. With as great as DNA polymerase is, DNA polymerase
can’t figure out where to get started without something called a primer. Primase makes the primer so that DNA polymerase
can figure out where to go to start to work. You know what’s kind of interesting about
the primer it makes? The primer is actually made of RNA. Ligase- the gluer. It helps glue DNA fragments together. More about why you would need that later on. Now, don’t feel overwhelmed. We’ll go over the basics of this sequence
in order. But remember, like all of our videos, we tend
to give the big picture. There are always more details and exceptions
to every biological process that we can’t include in such a short video. DNA replication starts at a certain part called
the origin. Usually this part is identified by certain
DNA sequences. At the origin, helicase (the unzipping enzyme)
comes in and unwinds the DNA. Here’s the thing though: you don’t want
these strands to come back together. So SSB Proteins (which stands for single stranded
binding proteins) bind to the DNA strands to keep them separated. And topoisomerase—I always have to slow
down when I say that enzyme’s name—keeps the DNA from supercoiling. Supercoiling might sound super and it can
be when you’re trying to compact DNA, but it’s something that needs to be controlled
during DNA replication. Supercoiling can involve an over-winding of
the DNA, and you need the DNA strands to be separated for the next steps. Primase comes in and makes RNA primers on
both strands. This is really important because otherwise
DNA polymerase won’t know where to start. In comes DNA Polymerase. Ok, before we go on, remember how we said
DNA has two strands? They’re not identical; they complement each
other. In our video that covers DNA structure, we
talk about how the bases pair together with hydrogen bonds. The base adenine goes with base thymine and
the base guanine goes with the base cytosine. These strands are also anti-parallel so they
don’t go in the same direction. What do we mean by direction? Well, with DNA, we don’t say North or South. We say DNA either goes 5’ to 3’ or 3’
to 5’. What in the world does that mean? Well, the sugar of DNA is part of the backbone
of DNA. It has carbons. The carbons on the sugar are numbered right
after the oxygen in a clockwise direction. 1’, 2’, 3’, 4’ and 5.’ The 5’ carbon is actually outside of this
ring structure. Now you do the same thing for the other side
but keep in mind DNA strands are anti-parallel to each other. So let’s count these—again, clockwise
after the oxygen. 1’, 2’ 3’, 4’ 5’. And the 5’ is out of this ring. This strand on the left runs 5’ to 3’
and the strand here on the right here runs 3’ to 5’. We’ll explain why all that matters in a
moment. So let’s take that knowledge there and look
at DNA replication here. In this image, I labeled the top original
strand 3’ to 5’. I labeled this bottom original strand 5’
to 3’. That’s the original DNA that is going to
be replicated. DNA is unwinding here thanks to helicase. In this example, it will keep unwinding in
this direction. Primase places primers. DNA polymerase is building the new strands. Now the thing about DNA polymerase is, when
it’s building a new strand, it can only build the new strand in the 5’ to 3’ direction,
meaning it adds new bases to the 3’ end on the new strand. See how it’s being built in the 5’ to
3’ direction? This one is called the leading strand. But, take a look down here. So DNA polymerase once again is building a
new strand in the 5’ to 3’ direction. But there’s a bit of a problem here. See, as DNA unwinds, because DNA polymerase
can only build the new strand in the 5’ to 3’ direction, it has to keep racing up
here next to where this unwinding is happening. You can see why then this new strand is known
as the lagging strand. On this lagging strand, primers have to keep
being placed in order for DNA polymerase to build. These fragments that result are known as Okazaki
fragments. Primers have to get replaced with DNA bases
since the primers were made of RNA. Ligase, the gluing enzyme as I like to nickname
it, has to take care of the gaps between the Okazaki fragments, sealing them together. At the end of this replicating, you have two
identical double helix DNA molecules from your one original double helix DNA molecule. We call it semi-conservative because the two
copies each contain one old original strand and one newly made one. One last thing. Surely you have had to proofread your work
before to catch errors? In this process, you don’t want DNA polymerase
to make errors. If it matches the wrong DNA bases, then you
could have an incorrectly coded gene…which could ultimately end up in an incorrect protein—or
no protein. DNA polymerase is awesome; it has proofreading
ability. Meaning, it so rarely makes a mistake. Which is a good thing. So, remember how we said there is far more
detail to this process to explore? The detailed understanding of DNA replication
has led to some lifesaving medical treatments that can stop DNA replication in harmful cells
including pathogenic bacteria or human cancer cells. We encourage you to explore beyond the basics;
check out the further reading suggestions in the video details to explore more! Well, that’s it for the Amoeba Sisters and
we remind you to stay curious.

Add a Comment

Your email address will not be published. Required fields are marked *