Hello all! This week in AP Bio we focused on learning about the central dogma and gene expression.
Initiation is when RNA polymerase attaches to a promoter region in front “upstream” of a gene. In prokaryotes, the RNA poly binds directly to the promoter. In eukaryotes, the RNA poly requires an assemblage of transcription factor proteins to be able to bind to the promoter.
Elongation is when RNA production occurs in a 5’ to 3’ direction. The template strand of DNA is the one that the RNA transcript is being produced off of complementary nucleotides. The nontemplate strand or coding strand of the dna will have the same.
Termination is when transcript production continues until end of the transcription unit is reached. There are multiple mechanisms of termination, teo examples from prokaryotes are:
-Rho-independent: the transcript based hydrogen bond with themselves, fold back and pull the transcript out of RNA polymerase.
-Rho-dependent: the rho protein destabilizes the RNA-DNA hydrogen bonding at RNA polymerase and ceases transcription.
What happens next? Many kinds of RNA. Unlike DNA, RNA plays many roles in the cell. There are around 10 described types of RNA , each with different functions, but there are three major types:
-Messenger RNA: carrried DNA sequence information to the ribosome
-Transfer RNA: carries specific amino acids to the ribosome
-Ribosomal RNA: major structural building block of ribosomes
In prokaryotes, the mRNA transcript is immediately translated. In eukaryotes, the mRNA is extensively processed in nucleus before it leaves to be translated.
Post-transcriptional mRNA processing happens in eukaryotes ONLY. There’s a 5’ cap and poly-A tail: A modified nucleotide is added to 5’ end, which gives it directionality, and a tail of several hundred adenine residues put on 3’ end of transcript, which allows it to move out of cell and gives it directionality.
In exon splicing, eukaryotic genes contain large stretches of non-coding DNA (introns) interspersed between coding DNA (Exons). To produce a functional protein, introns must be removed and exits must be spliced together prior to movement of mRNA transcript to nucleus. This process is accomplished by a spliceosome (a type of enzymatic RNA molecule).
Why introns? This is not answered. It could be evolutionary baggage or maybe S elfish genes. We know that having multiple exons in a gene allows eukaryotes to make multiple functional proteins from one gene (alternative splicing).
Translation:
Ribosomes are the S ite of protein synthesis. It’s the only “non-membrane” bound organelle. All cells have them. They’re composed of two subunits. They have three sites:
-A site: “aminoacyl”- where amino acids enter the ribosome
-P site: “peptidyl”- where the growing polypeptide is kept
-E site: “exit”- where empty tRNA molecules leave
tRNA transfers RNA molecules and are responsible for bringing amino acids to the ribosome. Amino acids are added to tRNA molecules through the action of “amino-acyl tRNA synthase” enzymes. A tRNA with an amino acid attached is said to be “charged”.
The genetic code is universal across all domains of life. The triplet code is when mRNA is read in united of three bases (codons). There are 64 possible codons (for 20 possible amino acids). The code is redundant and unambiguous, and has “start” and “stop”.
This week was interesting learning about all of this! Looking forward to diving deeper as it is still kinda confusing!