DNA Replication And Repair Flashcards
by convention the base sequence of nucleic acid strand is written as
5’ to 3’(if not mentioned, it means its from 5’)
if from 3’ to 5’ it should be mentioned in the sequence
m
m
chargaff rule
no. of purines= no.of pyrimidines
B DNA
watson crick model
right handed double helical structure
which bonds are broken during denaturation
H bonds only leading to ssDNA
NOT covalent(including phosphodiesterase bonds)
what is positive and negative supercoiling
POSITIVE
if the DNA wound more loosely than the WC dna
NRGATIVE
if the DNA wound more tightly than the watson crick dna.
req for most biologic reactions
fxn of topoisomerases
change the amount of supercoiling in dna
basic packing unit of chromatin
nucleosome
heterochromatin
tightly condensed
areas of chromosomes not expressed
nucleosome(10 nm chromatin) is made up of
- DNA
- two copies of each of the following histones
H2A H2B H3 H4 forming histone octamer
where is H1 located and its fxn
ass with linker DNA bw nucleosomes
helps in further packing to solenoid like structure(30nm fibre)
how many origin of replication are there in prokaryotic dna
only 1
replication is bidirectional
true
at a Origin of replication 2 replication forks are created that move in opposite direction
dna pol has proof reading activity whereas rna pol does not
yes
3’ to 5 ‘ exonuclease proof reading activity
dna pol requires a primer but rna pol does not?
true
dna pol can not initiate strand synthesis.
they can only extend the strand from 3’ end of primer.
role of dna pol I in prokaryotes
removes primer (as in okazaki fragments) due to 5’ exonuclease activity and synthseise new dna from 3’ end of neighbouring okazaki fragments.
the fragments are sealed by dna ligase
drugs acting on bacterial and human topoisomerases
quinolones
etoposide, teniposide
unwinding of the dna done by
helicase
break the double stranded dna i.e. H bonds
quinòlones target
topoisomerase II/ DNA gyrase
resp for negative supercoiling
whatvare the different eukaryotic dna pol
alpha, delta- dna synthisis
gamma-mitichondrial dna syn
beta, epsilon-dna repair
dna syn in prokaryotes by
dna pol III
removal of the rna primers by
eukar- RNAHase
prokar- DNA pol I
both have 5’to 3’ exonuclease activity
replacement of rna with dna in primer during replication by
eukar-DNA pol delta
prokar- DNA pol I
okazaki fragments are joined via
dna ligase in both eu/prokaryotes