DNA Flashcards
nucleic acids
- genetic material stored here
- passed from generation to generation via DNA and in some cases RNA (viruses)
circular chromosomes
prokaryotes
linear chromosomes
eukaryotes
plasmids
prokaryotes and sometimes eukaryotes
monomer of dna
nucleotide
polymer of dna
nucleic acid
exons
areas that code for genes
introns
areas that don’t code for genes (junk)
base pair rules
A binds to T with 2 H bonds
G binds to C with 3 H bonds
shape of dna
double helix
purines
- 2 carbon rings
- guanine and adenine
pyrimidines
- 1 carbon ring
- thymine, cytosine, uracil
covalent bonds
between the phosphates and deoxyribose and nitrogenous bases
speed of dna replication
- extremely rapid
- in prokaryotes, up to 500 nucleotides added a second
accuracy of dna replication
- very accurate
- only about 1 in a billion nucleotides is incorrectly paired
origins of replication
- dna replication begins here
- have a specific sequence of nucleotides
helicases
unwind the parental double helix and initiate replication
replication fork
the shape formed as helicase unwinds dna
replication bubble
zones where replication are occurring that you can see
single strand binding proteins
keep the separated strands apart and stabilize the unwound dna
topoisomerase
prevents the areas above the forks from kinking
primase
lays down primer (complementary to dna and about 10 nucleotides long) to start the addition of of new nucleotides
dna polymerase
- catalyze synthesis of a new dna strand according to base pairing rules
- new nucleotides align themselves along the templates of the old dna strand and dna polymerase links the nucleotide to the growing strand
direction of replication
grow in the 5’ to 3’ direction since new nucleotides are only added to the 3’ end of the the growing strand
leading strand
continuous synthesis - grows 5’ to 3’
lagging strand
discontinuous synthesis - produced in Okazaki fragments
Okazaki fragment
100-2000 nucleotides, synthesized in the 5’ to 3’ direction
dna ligase
joins okazaki fragments - forms covalent bonds between the 3’ end of each new fragment to 5’ end of growing chain
mistakes in base pairs
= mutation, changes dna -> changes rna-> changes proteins -> changes phenotype -> evolution
mismatch repair
- corrects mistakes while new dna is being synthesized
- dna polymerase each newly added nucleotide against its template; if incorrect the enzyme removes and replaces before continuing
excision repair
- corrects accidental changes that occur in existing dna
- these changes may result from reactive chemical, radioactivity, x rays, ultraviolet light
repair enzymes
- 50 types of dna repair enzymes
- the damaged segment is cut out by one repair enzyme and the remaining gap is filled in by base pairing nucleotides with the undamaged strand, dna polymerase and ligase catalyze the filling in process