gen bio 2 exam 3 Flashcards
How many proteins can a cell have?
5000
DNA ->?->RNA->?->protein
Transcription
Translation
Nucleotide
Phosphate, Sugar, Nitrogenous base
What are the nitrogenous bases?
Purines: Adenine, guanine
Pyrimidines: Cytosine, Thymine, Uracil
Nulceoside
Pentose sugar + nitrogenous page
Difference between ribose and deoxyribose
Ribose has an extra o at c’2
Attatchments of Nucleotide
Phosphates attach to c5’, bases attach to c1’, and second nitrogenous bases in chain attached to c3’
Complimentary strands of 5’->3’
Semiconservative Replication
When DNA is duplicated, the resulting daughter strands are 1/2 nascent, and 1/2 parent
Lagging Strand
The bottom strand in duplication runs 5’->3’, but duplication needs to go 5’->3’ so RNA primease makes primers where RNA polymerase then runs 5’->3’
Okazaki Fragment
Fragments of lagging strand, DNNA polymerase removes the primers and ligase connects the fragments
DNA Polymerase
Reads the parent strand and synthesis the daughter DNA, at 50 bases/second, 1/100,000 bases are mutated.
Ways to fix errors in DNA replication
- DNA polymerase can correct its own mistakes
- Mismatch repair is where a second DNA polymerase proofreads, and when it comes across and error it cuts out a section around the error, and ligase puts new section in
- Excision Repair: extra nucleotide inserted, and Polymerase cuts it out and a ligase repairs
Telomeres
Repeated TTAGGG 200-2500 times to form a cap at the end of DNA, as due to DNA polymerase running 5’->3’ and a primer is needed, a few nucleotides are lost at the caps
Many cancer cells have active telomerase which repairs the telomere caps
3 main types of RNA
mRNA - messenger RNA
tRNA - Transfer RNA
rRNA - Ribosomal RNA
Transcription, 3 main steps and what is needed (transcription)
What is needed:
1) precursors (ATp,GTP,CTP,UTP)
2) energy (ATP)
3) enzymes (RNA polymerase)
4) Template (DNA)
3 main steps:
1)Initiation
2)Elongation
3)Termination
Initiation (transcription)
Promoter (section of DNA where the polymerase attaches to)
Elongation (transcription)
DNA is unwinded in the bubble, RNA polymerase adds RNA nucleotides to the template strand )5’->3’)
Termination (transcription)
Termination sequence is section of DNA that makes the RNA polymerase detatch, then DNA winds back
5’ cap
a 5’ cap is added to pre-mRNA, added to the 5’ end and is 7-mehtylguanine.
Helps stabilize mRNA
Assists w/ ribosome loading
poly A tail
added to the 3’ end, hundreds of adenines
helps stabalize mRNA
helps w/ nuclear export
Splicing
occurs to mRNA, introns are removed by snRNPs that form a spliceosome
Translation
INITIATION
tRNA attatched to the small subunit, and then the large ribosomal subunit attatches.
ELONGATION
The anti-codon matches w/ codon, and when the amino acid is attatched the ribosome move forward 1 codon on the mRNA, and the tRNA moves to the exit site and a new tRNA enters the A site before movement. This repeats ntil termination sequence
TERMINATIOn
when termination codon is met (UUA, UGA, UAG) a termination factor attatches to the P site, and complex dissasembles
Start and end codons
Start ; AUG
End: UUA, UAG, UGA
Polyribosomes
Have a bunch of ribosomes translating one mRNA at once