Finishing chapter 7.
RNA polymerase binds to the promoter with the help of what.
One race opens up the DNA (separates the two strands).
Going to pay attention to one strand and not pay attention to the other.
The template is the guide to make the RNA.
No template strand.
mRNA.
RNA transcript.
Add five five cap.
Modified guanine.
The cap changes the shape of that end of the transcript so enzymes in the cytoplasm do not recognize it as nucleic acid and do not destroy it.
Protects the beginning end from degradation in the cytoplasm by those nuclease enzymes, hydrolytic nuclease enzymes.
Add a polyhalide tail.
Three prime poly HCl.
A long series of a's is added to this.
Does not prevent the nuclease enzymes from digesting, breaking down, or hydrolyzing this molecule; just slows it down.
The a's are flying over its shoulder as it goes through.
Slowly breaks down the covalent bonds between the nucleotide and separating them.
Eventually, it will get to the gene and degrade the gene, and you can't make any more proteins out of it.
If you have a longer tail, the transcript will persist longer, and you can make more protein out of it.
If you have a shorter tail, it persists for a brief period of time, and you can make less protein out of it.
It is one way that the cell can regulate how much protein it makes from each transcript.
mRNA now.
Some sections of this are not going to be used.
AGCPUs.
The parts we don't use are going to be cut out.
Those units that are removed are called introns.
Stands for intervening region.
In the way region.
Remove the introns.
The parts that are left are called exons.
Exon stands for expressed region.
Exon a b c d and intron one two three.
Remove the three one, two, and three parts and splice back or glue back the other parts, third a, b, c, and d.
Generally, about 90% of the transcript is actually gonna be removed in the steps.
It is possible for one transcript to be edited differently.
Variable splicing that can occur to make different proteins out of the same transcript.
Human Genome Project.
Transcript (mRNA) leaves the nucleus and goes to the cytoplasm due to translation.
Addition of the modified cap also enables it to bind with transporters in the nuclear envelope, the nuclear membrane, and help it be exported.
It won't be exported until it's been modified.
We've got the mRNA.
Ribosomes.
Other RNAs.
tRNA.
rRNA.
mRNA.
Leader sequence or untranslated section or region mRNA.
Translation will begin a little bit further.
First part.
Role:
Helps it exit the nucleus.
Helps it bind to a ribosome that binds its way, but it's not going to be translated.
The first one that starts off as AUG.
The ribosome is going to translate this mRNA three bases at a time.
Three bases are sometimes called a triplet.
Codon - Your book uses that term codon.
The first codon that is translated reads AUG, a start codon.
Piece of RNA.
Hairpin moving up one side.
Another hairpin moving another side.
Comes back, has another hairpin move, another side, and it kinda comes back.
There is complementary base pairing that occurs along those hairpin moves.
Holds it together but then it folds over on itself.
Not very rigid because they are very flexible.
Two of these ends are important, and the others do not.
This end up here that's still kinda sticky that we haven't started with.
This part here finds an amino acid.
Another name for amino acid is peptide Binding site.
At the other end, we've got more RNA bases in here.
Those don't actually bind anything.
These three are kind of twisted on the outside the binding on the small one.
These three are referred to as the anticodon.
A list of all the codons (not anticodons) and their corresponding amino acid that would be on the tRNA with the complementary anticodon.
Codons
AUG
*AUU, AUC, and AUA
*CCU, CCC, CCA, CCG
Redundancy.
Start codon - AUG
Stop codons: UAA, UAG, and UGA.
64 different possible combinations of four different letters taken three at a time (20 amino acids).
Wobble: The flexibility of that third base.
Initiation, elongation, and termination.
the beginning, middle, and end.
The first thing that's gonna happen is the ribosome, which I haven't talked about yet, has two parts to it.
One's big, one's small.
It is going to come in and clamp on to where that start going on is.
That first tRNA is also going to bind.
Ribosome.
*Ribosome is protein
Ribosome is basically just a really big enzyme. And enzymes tend to be protein.
Ribosome is made up of a lot of protein (a bunch of amino acid chains that have been folded up).
Ribosome also has a bunch of RNA into it.
Combination of protein and nucleic acid.
Made up of 50% DNA and 50% protein- Chromosome.
Move down the mRNA three bases at a time.
*Ribosome has a couple of binding sites with two active sites. The ribosome can accommodate two different tRNAs at a time.
tRNA stands for transfer RNA.
Transfer RNA transfer the amino acid.
mRNA
Messenger RNA.
The message is that RNA is the instructions.
It's gluing the message of instructions for the sequence.
rRNA
Ribosomal.
The RNA that's in the red zone.
Transcription factors.
Poly A and L.
How the DNA is folded can make certain genes available and unavailable.
Developmental genes when you're an embryo that were being utilized and now you don't use those anymore.
*Chromatin is just the wrapped-up DNA.
*Chromatin is actually divided into two different types of chromatin
*Euchromatin is more open
*Heterochromatin is more closed.
Another way of making genes available or unavailable is called methylation. Add methyl groups such as that c h three functional group to the outside of the DNA, and that prevents the transcription factors from binding. The transcription factors can't bind.
Methylating a region of DNA can prevent transcription from occurring.
These are modifications that occur to the outside of the DNA, we call this epigenetics.
Changes outside of the DNA sequence.
Epigenetic changes can persist from one generation to the next.
Alternative splicing.
RNA export.
Make little RNAs or microRNAs.
The cell can make little RNAs or microRNAs.
They don't go for a protein.
They're not part of tRNA.
They're not part of RNA.
They're their own thing called microRNA.
MicroRNAs are complementary to a region on an RNA, so they're specific to an RNA.
If the cell makes those, they will bind to the mRNA in the cytoplasm and block the ribosomes, essentially turning that gene off. No protein will be made to block translation.
MicroRNAs; They will bind to the mRNA in the cytoplasm and block the ribosomes, essentially turning that gene off. No protein will be made to block translation.
Degrade some faster than others; The polyatail
A mutation is simply a change to the DNA.
Interested in changes to DNA that will affect the protein of the backside of translation.
Interested in in changes to the DNA that affect the proteins.
It is when we say affect protein, we mean the amino acid sequence is altered.
Mutations are a natural part of of life.
Selective breeding for these different grapes.
Two different types of mutations.
Point mutations
A point mutation is when a single amino acid has been changed; A single nucleotide has been changed.
Wild type is the one that's the most common (the version that's most common in the population).
Mutant type is any of the versions that are not the most common version.
Black is wild type for humans, black hair.
Substitution (one base is changed for another)
Insertion (a is added)
Deletion (would be removed)
A substitution tends to change one amino acid in the sequence.
An insertion will change every amino acid downstream from the insertion of the deletion point (alot of different amino acids).
*One amino acid, the protein may work. It may work better. It may work worse. It may work well enough. A bunch of them change, that thing's not gonna work. That protein's not gonna work.
Silent mutation:
No change to the amino acids.
Missense mutation:
Change one amino acid.
*Sickle cell anemia is caused by substitution and one single amino acid is different in the chain of about a thousand, and that's enough to cause the red blood cells, the hemoglobin, and the red blood cells to form a sickle shape from the wash. So it's a missense mutation.
Nonsense mutation:
Premature stop codon that shows up, and ends translation at that point.
Frameshift mutation:
When you change the reading frame and you mess up all your amino acids downstream.
Two gene, Sometimes called language gene.
Humans have a duplication of that gene.
Humans can talk.
Neanderthals also have a duplication.
*It has to do with the brain development in the broca region, which is where you kinda communication the language part of your brain.