#Transcription

The activation and transcription of genes.
1/ The DNA of the cell serves as a master blue print. Every cell of our body has a complete copy of this
DNA blueprint. Depending on the cell and its functions, it will use specific parts of the blueprint found in the DNA to produce the proteins and enzymes needed by that cell.
2/ The rule is that each gene creates
one fully functional protein or enzyme. Image
3/ The gene itself has a few key regions that are important to be familiar with. The very first nucleotide to be copied is the start of the actual gene. The part that in copied is called the open reading frame. Image
4/ The gene includes all the nucleotides that make up the actual messenger RNA. About 50 to 100 nucleotides before the start site will be the
promoter region. The most basic part of the promoter is called the TATA box. Its a sequence of
Thymine and Adenine nucleotides.
5/ This is the most basic promoter region and allows for a low level of gene expression. The transcription factors will bind to the promoter region and increase the level of gene expression. That means more copies will be made of that gene.
6/ When transcription begins, the RNA polymerase will bind to the promoter and begin copying the gene. Image
7/ There is actually a big complex of proteins that must bind to the promoter region before the RNA polymerase. This is called the initiation complex. It starts with the TATA binding protein (TBP) and builds this complex that recruits RNA polymerase.
8/ There are other regulatory segments in the DNA that can influence gene expression. They are called
regulatory elements and are located thousands of nucleotides before the promoter. Image
9/ They can bind transcription factors called Repressors or Enhancers. The DNA will fold in a loop which allows the regulatory sequence to come in contact with the promoter region.
10/ This will allow the Repressor to block binding of the RNA polymerase. The Enhancer can also make contact with the RNA polymerase, but it will increase the activity of the RNA polymerase leading to increased gene expression.
11/ Once the transcription factors have bound to the promoter region, the RNA polymerase can bind to the
transcription factors and begin copying the gene.
12/ The RNA polymerase opens up the DNA itself. It
doesn't need any assistance like the DNA polymerase did. It will begin copying the DNA using the 3' to
5' strand of DNA as a template and create a RNA strand in the 5' to 3' direction.
13/ It begins with the first start nucleotide and continues until it reaches the end point. Then the polymerase will fall off and the RNA strand will be free to move into post transcriptional modification. Image
14/ The initial strand of the RNA is called the primary transcript. It will undergo three modifications before
it can leave the nucleus of the cell. The first is it will undergo splicing by the spliceosome complex.
15/ The vast majority of the gene is made up of non coding information called introns. The actual coding part of the gene is called the exons. The spliceosome will follow splicing marks on the primary RNA and
remove all the introns and paste the exons back together. Image
16/ This also leads to the ability of alternative
splicing by cells to use a gene differently. One cell might use Exons 1, 2, 4, and 5 while another might
use Exons 1, 3, 4 and 5. That is the concept of alternative splicing. Image
17/ Two different proteins can be made from the same gene, but by different splicing of the exons.
18/ After the splicing of the RNA is complete, there are enzymes that will add a Guanine cap to the 5' end
of the RNA. This serves to allow the RNA to exit the nucleus and assists in loading the RNA into the
Ribosome. Image
19/ The last process is the addition of the poly A tail. This just adds about 250 or more Adenine
nucleotides to the end of the RNA. This signifies the end of the RNA when its read by the Ribosome.
20/ The final RNA product is now called a messenger RNA (mRNA). Its built to take the DNA information
and deliver it to the Ribosome for production of a protein.

• • •

Missing some Tweet in this thread? You can try to force a refresh
 

Keep Current with Biotech2k

Biotech2k Profile picture

Stay in touch and get notified when new unrolls are available from this author!

Read all threads

This Thread may be Removed Anytime!

PDF

Twitter may remove this content at anytime! Save it as PDF for later use!

Try unrolling a thread yourself!

how to unroll video
  1. Follow @ThreadReaderApp to mention us!

  2. From a Twitter thread mention us with a keyword "unroll"
@threadreaderapp unroll

Practice here first or read more on our help page!

More from @Biotech2k1

15 Sep
#Cancer_Immunology TME

A look into the Tumor Micro Environment (TME).
1/ There is a complex set of interactions that must go on between a tumor and its surroundings. It has to interact with the tissue cells, it needs nutrients, it needs oxygen, it needs to survive and proliferate in a hostile environment.
2/ One of the many things it has to achieve to exist and thrive is to overcome the immune system and its natural ability to find, target and destroy tumors. There are 3 key cells in the immune system that are designed to find and kill cells that are infected or defective.
Read 19 tweets
15 Sep
My Game Plan:

Pathways:
$BPMC 3.37% core position
$MRTX 3.37% core position
$TPTX 3.37% core position
$SDGR 1.35%
$RVMD 2.7%
$RLAY 2.7%
$ERAS 0% considering but way too expensive
$RPTX 2.02%
$KNTE sold out as it was my weakest link
Protein Degraders:
$ARVN 1.35%
$KYMR 1.35% paying down a core position
$CCCC 2.02% paying down a core position
$GLUE 1.35% paying down a core position
CRISPR/Old Antibodies
$CRBU 1.35% paying down a core position
$BCAB 2.7% will sell out when I think its good opportunity.

CRISPR is way to crazy on values to waste money on here. It will implode someday, and I will be waiting.
Read 6 tweets
15 Sep
#Targeted_Protein_Degradation

A look into protein degraders.
1/ There are 2 types of protein degraders in development and a 3rd in concept phase of development. The first is the monoDAC, the second is the biDAC and the last is the triDAC.
2/ The monoDAC will bind with a covalent chemical bonding to the E3 ligase and alter its targeted function. It changes the shape of the E3 and directs it to place the ubiquitin molecule onto a protein it directs.
Read 7 tweets
15 Sep
#The_Proteasome

I look at how the Proteasome works.
1/ The Proteasome is a cellular organelle. Its like the recycling bin for proteins. When a cell is done with a protein, it tags it for destruction in the process called ubiquitination.
2/ The proteasome will load these tagged proteins and break them down into peptides of about 7 to 10 amino acids in length for recycling. They will further be broken down after into single amino acids for reuse to build new proteins.
Read 7 tweets
15 Sep
#Ubiquitination

A look at ubiquitination.
1/ Cells make, regulate and break down proteins constantly. They have a system to control the regulation of the proteins they produce. This is to remove unwanted proteins when no longer used.
2/ It also maintains healthy proteins as they degrade slowly over time. The process of ubiquitination is the tagging of these proteins by the cell for destruction. There are 3 enzymes that work in the process of ubiquitination.
Read 10 tweets

Did Thread Reader help you today?

Support us! We are indie developers!


This site is made by just two indie developers on a laptop doing marketing, support and development! Read more about the story.

Become a Premium Member ($3/month or $30/year) and get exclusive features!

Become Premium

Too expensive? Make a small donation by buying us coffee ($5) or help with server cost ($10)

Donate via Paypal Become our Patreon

Thank you for your support!

Follow Us on Twitter!

:(