DNA Part 2 Flashcards
Where are the control mechanisms in Eukaryotes?
DNA to RNA is a control point5 prime G cap is a control point 3 prime Poly A tail is a control point A splicing reaction to connect exons together and to remove introns, this is a control pointIf we take the messege out of the nucleus is a control point. TRANSCRIPTIONAL CONTROL POINTS If DNA is packaged there is NO TRANSCRIPTION If DNA is mentholated there is NO TRANSCRIPTION
What are Histones?
Are proteinA
They package DNA
They are positive - Lysine, Arginine, histidine
What is Histone Acytlease?
is going to cover up the positive charges, it also unwinds DNA
What do we have to do in order to start transcription?
If we want to start transcription we have to unwind DNA which means we have to cover up the positive charges with Histone Acytlase.
Histone acytlase adds an acytle group to the histone, the acytle group then removes the possitive charge
Histone acytlase adds an acytle group to the histone, the acytle group removes the possitive charge
Once we cover up the positive charges the TF and the RNA polymerase can start binding to the DNA, they cant do that until we unwind the structure of the DNA.
Once we cover up the positive charges the TF and the RNA polymerase can start binding to the DNA, they cant do that until we unwind the structure of the DNA.
What needs to happen in oder for transcription to occur?
we have to unwind the DNA and remove the methol groups
What is a promoter?
Is that region of DNA that tells us where transcription is going to occur and it is bound by RNA Polymerase. (it has a fixed location it is always going to occur just upstream of where transcription is going to start where RNA Polymerase
What is an Enhancer?
The enhancer does not have a fixed location, it can lie anywhere within the structure of DNA, and the enhancer is not bound by RNA Polymerase. It is bound by activators and inhibitors. It can either turn the process on or off.
The enhancer can lie anywhere in the DNA sequence in the linear form, but when DNA is folded the enhancer and the promoter lie side by side, this is going to help RNA Polymerase bind to the promoter site
The enhancer can lie anywhere in the DNA sequence in the linear form, but when DNA is folded the enhancer and the promoter lie side by side, this is going to help RNA Polymerase bind to the promoter site
Why are cells different than each other?
Because of the enhancer ,the activators and the inhibitors. Each type of cell will have a different set of activators and inhibitors.
If DNA is packaged there will be no transcription, if it is methylated there will be no transcription, we also have to see what activators and inhibitors are present this will determine what genes will be turned off or on.
If DNA is packaged there will be no transcription, if it is methylated there will be no transcription, we also have to see what activators and inhibitors are present this will determine what genes will be turned off or on.
Post Transcriptional Control - What do we do to the RNA after we have made RNA,
we add a 5 prime Gcap, we had 3 prime Poly Tail, we add these two so we know when transcription is over, and we have to have this so that we have transportation out of the nucleus and into the cytoplasm and it prevents derogation. We also have to think of the splicing reaction, this is where we connect the exons together and we cut out and throw away the introns.
Translational control
Getting the message to a ribosome and having translation occur.
Post Translational Control - What happens to the protein after we have made it?
We have to fold it into its correct 3d shape, because when a proteins first comes off the ribosome it is linear, but linear proteins cant do anything it must fold into its complex 3d shape. (example insulin)