EXAM 3 P2 Flashcards
central dogma
all DNA in cells is double stranded (dsDNA)
the two strands are antiparallel
held together by base pairing (CGAT)
purines
A and G
pyrimidines
T and C
single stranded DNA
only found in viruses
DNA structure of bacteria
singular circular chromosome
single origin of replication
no histones
DNA structure of archaea
single circular chromosome
1-3 origins of replication
contains histones
DNA structure of eukarya
multiple linear chromosomes
man origins of replication on each chromosome
contains histones
DNA polymerase
carries out DNA replication & repairs damaged DNA
requires an RNA primer to initiate synthesis
binds to the template strand and needs some form of nucleic acid (DNA/RNA) with a 3 prime end. bases are added to the 3’ end. synthesis is 5’ to 3’
proofreading ability
used by DNA polymerase to ensure fidelity of DNA replication.
first method to make sure no mistakes are made
exonuclease activity
explain the process of DNA replication
starts at the origin of replication. DNA poly starts moving around the circle in both directions (saves time)
point of movement around the circle is the replication fork, where the 2 strands are spread apart. once they meet at the bottom 2 identical progeny are produced
aka theta-form replication
DnaA
protein that recognizes the origin of replication and recruits other proteins to start the process
determines when and where we start
lagging strand
synthesis is discontinuous
made in a series of short pieces
leading strand
synthesis is continuous
helicase
replication protein that unwinds the two strands of the original molecule
primase
protein that synthesizes an RNA primer
single-stranded binding proteins
bind to a small amount of single stranded DNA to protect it damage and prevents reannealing to dsDNA
okazaki fragments
series of short DNA pieces made in lagging strand synthesis, about 2000 bases long
tau
holds everything together during replication
DNA polymerase 3
does about 99% of chromosome replication in bacteria
really fast
filling the gaps between okazaki fragments
DNA poly 3 synthesizes fragments and stops if no template strand is present, creating a gap in the DNA
DNA poly 1 uses exonuclease activity to remove RNA bases and fill in the gaps
the nicks are sealed by connecting the 3’ and 5’ ends
the two fragments are now one strand
operons
has one promoter, multiple genes, and a terminator
polycistronic DNA, mRNA produced from the operon is also polycistronic
one promoter activates all the genes
RNA polymerase
bacterial RNAP has 1 core enzyme made of 4 essential subunits, plus a sigma
eukaryotic has many subunits
core enzyme binds to sigma. sigma recognizes the promoter from a recognizable sequence of bases
core enzymes
can bind to single strands but they aren’t smart
if mixed with DNA, it will start at random spots
doesn’t know where to stop
-10 and -35 regions
areas of recognition for the sigma subunit
-10 is also the pribnow box
+1
first base in the RNA product
place where transcription starts when RNA binds to the promoter
consensus sequence for sigma A
the best sequence for sigma A to recognize promoters
TTGACA