Exam 3 Flashcards
(51 cards)
Initiator proteins
breaks H bonds to initiate replication
Primer
short nucleotide sequence that initiates DNA polymerase binding
Primase
RNA polymerase that creates primers
For proofreading to take place…
DNA must be copied in 5 - 3’ direction
why is it 5’ to 3’
energy from triphosphate on oncoming 5’ end gives energy for reaction
Telomerase
Adds bases 5’ to 3’ to the lagging template strand
*Extends the template strand so DNA replication proteins can replicate
lagging strand and it does not shrink with each cell division.
Depurination
G lost
Deamination
C turns to U
Mismatch repair system
Excision - damage is
recognized and cut out by one of a
series of nucleases
resynthesis - original
DNA sequence is restored by a
repair DNA polymerase
Ligation - DNA ligase seals
the break left in the sugar–
phosphate backbone of the
repaired strand
Exonuclease
– remove bases from the end of a strand
Endonuclease
– remove bases from the middle/cut DNA or RNA
5’-3’ exonuclease activity
- Removing RNA primers made by primase
3’-5’ exonuclease activity
- Proofreading
Nucleases
– enzymes that remove nucleotides from DNA
Promoter v Terminator
Terminator transcribed, Promoted not
Promoter sequences at
-10, and -35 nucleotides down from start
Eukaryotic vs Prokaryotic regulatory proteins
Eukaryotic - multiple accessory proteins
- 3 RNA poly
Prokaryotic - one sigma factor
- 1 RNA poly
RNA poly 2
transcribes all proton coding genes
TFIID, TFIIH, and RNA poly II
TFIID - distorts DNA
TFIIH - opens up double helix
RNA Poly II - disassociates from other factors and starts transcription
Elongation Factors
Form a wedge on nucleosomes that allow RNA poly II to transcribe through proteins
cap and poly A tail
5’ cap Phosphate w/ modified guanine
Poly A tail
Effects from capping and polyadenylation
1) increase the stability of eukaryotic mRNA.
2) facilitate export to the cytosol
3) mark the molecule as an mRNA molecule
snRNP
recognizes splice sequences
U1, U2, U6
U1 recognizes the 5′ splice site
U2 recognizes the lariat branch-point site through
complementary base-pairing.
U6 then “double-checks” the 5′ splice site by displacing
U1 and base-pairing with the same intron sequence itself.