Differences in translation between prokaryotes and eukaryotes

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About this video

This video compares the mRNA used in translation in prokaryotes and eukaryotes. Prokaryotic mRNA uses a Shine-Dalgarno sequence as the ribosome binding site, while eukaryotic mRNA uses a 5' cap, plus a poly-A tail; both the cap and tail protect eukaryotic mRNA from degradation during its journey from nucleus to cytoplasm. Prokaryotes also start their polypeptide with formylmethionine, whereas eukaryotes start with methionine.

You'll be able to

  • compare the ribosome binding sites of prokaryotic and eukaryotic mRNA.
  • explain why eukaryotic mRNA needs a 5' cap and poly-A tail.
  • state the difference in the first amino acid between prokaryotes and eukaryotes.

Key words

Shine-Dalgarno sequence
The site on prokaryotic mRNA that the ribosome recognizes and binds to.
5' cap
A guanine nucleotide with a methyl group on eukaryotic mRNA; also the ribosome binding site in eukaryotes.
Poly-A tail
A long run of adenine nucleotides (about 100-250) on the 3' end of eukaryotic mRNA.
Start/stop codon
AUG starts translation and a stop codon ends it.
Formylmethionine
The first amino acid in prokaryotic polypeptides: methionine with a formyl group attached.
Transcript

- [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.

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