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46 Cards in this Set

  • Front
  • Back
semi-conservative replication
each daughter duplex contains one strand from each parental DNA
conservative replication
one daughter duplex is only parental DNA and the other is only newly synthesized DNA
dispersive replication
parental strands are fragmented and new strands are synthesized from them in fragments. Then they join together as a mix.
Bidirectional duplication
bacterial replication (on a circular chromosome)
gyrase
bacterial protein that overcomes unwinding problem by breaking and rejoining tightly coiled strand ahead of replication fork relieving tension
topoisomerase I/II
eukaryotic protein that overcomes unwinding problem by breaking and rejoining tightly coiled strand ahead of replication fork relieving tension.
DNA polymerase
synthesizes new DNA, requires a single stranded template and a primer
okazaki fragments
short strands on lagging strand
polymerase delta or sometime e
type of DNA polymerase in eukaryotic replication
polymerase III
type of DNA polymerase in bacterial replication
primase
initiates the synthesis of leading and lagging strands by placing RNA primers (in both bacterial and eukaryotes)
polymerase I
removes RNA primers in bacteria, and fills gap with DNA
DNA ligase
seals okazaki fragments into a continuous strand (both bacterial and eukaryotic)
primosome
is made up of helicase and primase
helicase
moves along DNA catalyzing the ATP-driven unwinding of duplex.
Single-stranded DNA-binding proteins (SSBs)
keeps the unwound DNA from reforming
5' to 3' exonuclease function
removes 10 nucleotides from 5' end which is key to removing RNA primer
3' to 5' exonuclease function
removes mispaired nucleotides from 3' end of growing DNA and is key to maintaing accuracy of DNA synthesis.
B (beta) sliding clamp
present in bacterial cells and allows DNA polymerase III to cycle on lagging strand. DNA polymerase III jumps clamp to clamp after each okazaki fragment is finished
DNA polymerase III holoenzyme (replisome) is made up of
two core polymerases which replicate DNA, two t-subunits which hold the core polymerases in the complex, two or more beta clamps allowing polymerase to stay on DNA, and a clamp loading (gamma) complex which loads each sliding clamp onto DNA.
autonomous replicating sequences (ARSs)
located in yeast and are sequences that promote replication
Origin recognition complex (ORC)
recognition of origin of replication (eukaryotes)
DnaA
recognition of origin of replication (bacteria)
Mcm (licensing factor)
involved in the steps leading to replication in eukaryotes, binds to origin during or following mitosis. IS A DNA HELICASE THAT UNWINDS PARENTAL DUPLEX (eukaryotes)
DnaB
DNA helicase that unwinds praental duplex (bacterial)
RFC
protein that loads the PCNA clamp onto the DNA (eukaryotes)
PCNA
ring-shaped subunit that clamps replicating polymerase to DNA (eukaryotes).
RPA
maintains DNA in a single-stranded state (eukaryotes)
Fen-1
removes RNA primers (eukaryotes)
DnaC
loads helicase onto DNA (only in bacteria, not sure what does in eukaryotes)
replication foci
localized sites in nucleus for replication activities
nucleosome
repeating subunit of chromatin, consists of DNA chain coiled around a core of histones
nuclease
a repair enzyme that recognizes a mismatched base pair by difference in geometry
XPC protein
damage recognition in global pathway is mediated by this protein (N.E.R.)
CSB protein (cockayne syndrome B)
damage recognition in the transcription-coupled pathway is mediated by this protein and a stalled RNA polymerase
XPB and XPD proteins
two helicase subunits of TFIIH and separate DNA strands (specifically in Nucelotide excision repair)
XPG
incision on 3' side during nucleotide excision repair
XPF-ERRCC1 complex
incision on 5' side during nucleotide excision repair
DNA glycosylase
initiates base excision repair by recognizing a mismatched base and cleaving the glycosidic bond holding the base to the sugar moiety.
endonuclease in base excision repair
performs the excision of deoxyribose phosphate
phosphodiesterase activity in B.E.R.
removes sugar-phosphate remnant
polymerase B in B.E.R.
fills in the gap by inserting complementary nucleotide
DNA ligase III
sealing step in B.E.R.
DNA ligase I
sealing step in N.E.R.
Ku protein
detects lesion in double-strand breaks and binds to the broken ends of DNA
DNA-PKcs
works with Ku protein to bring broken strands of DNA back together for DNA ligase to seal back together.