- [Voiceover] Let's talk
about some of the differences between how translation
happens in prokaryotic cells and how it happens in eukaryotic cells. And I want to focus mainly on the mRNA just before
it's ready to be translated. So let's start with our prokaryotic mRNA and let's look at our
five prime side first. So we have this yellow part right here, and that's the noncoding region. And it's called the noncoding region because the ribosome is not actually going to read that part. So that particular sequence of amino acid is not that important. And then after the noncoding region we have the Shine-Dalgarno sequence. And the Shine-Delgarno sequence is the site that the ribosome's going to recognize and bind to. So let's just throw a
ribosome right over here. This is where the prokaryotic
ribosome is going to bind. And then after the
Shine-Delgarno sequence, we have another noncoding region. Just gonna abbreviate it NCR. And then we have our start codon, which is typically AUG, so that tells us to start. And so the ribosome's
going to start translating, it's going to read this entire section, put together the corresponding
polypeptide chain, until it hits the stop codon, which tells it to stop translating. And then we have another noncoding region. Let's look at our eukaryotic mRNA. And so it's pretty similar, but you can see there
are some differences. So we'll start with our
five prime side first. So you see this red
nucleotide right over here. That's the five prime cap. And the five prime cap is
simply a guanine nucleotide. So I'm gonna draw a G inside, Guanine, and it's going to have a methyl group somewhere on the molecule. So I'm gonna draw a methyl group. And the bond between this guanine and the nucleotide right near it is a bond that's different than the bond that you'd typically find
between two nucleotides. And so that's really all
the five prime cap is. And the five prime cap is actually the ribosomal binding site in eukaryotes. So that means that in eukaryotes, the ribosome's going to recognize this particular part and bind to it. So after the five prime cap, we have this other noncoding region which the ribosome's
not going to translate. And then the ribosome is going
to hit the start codon again. AUG tells it to start, and
it's gonna start translating, so it's going to translate
this entire section until it hits the stop codon. And then we have another noncoding region. And then we hit something
that looks different than what we've seen in
the prokaryotic mRNA, so this section with blue nucleotides, and that's called the poly-A tail. And the poly-A tail is
a bunch of nucleotides that are all A's, or adenines, so I'm gonna draw A's inside
all of these nucleotides. And the poly-A tail is
actually pretty long, so it's typically anywhere between 100 and 250 nucleotides long. So that's pretty long. So I didn't exactly draw it to scale. And the purpose of both
the five prime cap, and the poly-A tail is to prevent this mRNA from being degraded by enzymes. So it acts as kind of a signal that does not allow enzymes to
break it down or degrade it. And so you might be wondering, well, what about prokaryotic mRNA? How come they don't have anything similar to prevent them from being degraded. And the brief answer to that question is that in prokaryotic cells, transcription, that's an R, and translation, both happen in the same place. So prokaryotic cells don't
exactly have a nucleus. They have this cytosol and transcription and translation are happening in the same place. And not only are they
happening in the same place, but they can actually be happening at the same time. So you can have a piece of mRNA that's being formed, and while it's being formed, a ribosome will attach to it
and being to translate it. But, in eukaryotic cells, things
are a little bit different. So transcription... happens in the nucleus, and translation happens in the cytoplasm where there are ribosomes. And so the mRNA, after it's made, has to travel, from the
nucleus to the cytoplasm to where the ribosomes are. And so because it's traveling this relatively large distance, it's going to encounter a
lot of different things, including enzymes that
might break it down. And so it needs this extra protection to prevent it from being
damaged in any way. There's one more difference
I want to talk about in how translation happens
in prokaryotes and eukaryotes and that is what the first amino acid in the polypeptide chain will be. So in prokaryotic cells,
the first amino acid in the chain is always formylmethionine. And formylmethionine is simply the amino acid methionine, but with a formyl group attached. And in case you don't remember what a formyl group looks like, it looks like that. In eukaryotic cells, the first amino acid in all the polypeptide
chains is simply methionine. And it's interesting to note that formylmethionine actually
acts as an alarm system in the human body. So if you had some
bacterial cells in your body that were damaged in any way, there would be these
formylmethionines floating around, and that tells your body that
there are bacteria around, and it's going to trigger
an immune response.