DNA Flashcards
DNA
genetic material of all living organisms
Griffith’s experiments
Transformation. Inject S- died, Inject R- live, inject dead S- live, inject dead S and live R- died
Avery’s experiments
used bacteria instead of mice
- destroyed protein-still had transformation
- destroyed DNA- no transformation
Hershey and Chase
used bacteriophage T2
used 35S and 32P to infect Ecoli (dna=P, protein=s)
infect bacteria, see if radioactivity ends up IN the cell
Watson and Crick
discovered that a DNA molecule consists of two polynucleotide chains twisted around each other into a right handed double helix
Each nucleotide consists of
- deoxyribose
- a phosphate group
- a base
Each full turn of double helix is…
10 base pairs
Rosalind Franklin
used X-ray diffraction to discover the shape of DNA
Semiconservative replication
two strands of parental DNA molecule unwind, each is a template for the synthesis of a complementary copy
Meselson-Stahl
bacteria grown in 15N (heavy) then transferred to 14N and allowed to grow and divide for several generations. Then, centrifuge. Before it was all 15N, then 15N and 14N hybrid after 2nd, and 14-14, and 15-14 after 3, showing it kept one parent strand
Helicase
unwinds the DNA
Primase
synthesizes RNA primer (starting point for nucleotide assembly by DNA polymerases)
DNA polymerases
assemble nucleotides into a chain (at 3’ end), remove primers, and fill resulting gaps
DNA ligase
closes remaining single-chain nicks
Single-stranded binding proteins
stabilize single-stranded DNA and prevent the two strands at the replication fork from reforming double stranded DNA
Topoisomerase
avoids twisting of the DNA ahead of the replication fork (in circular DNA) by cutting the DNA, turning the DNA on one side of the break in the direction opposite to that of the twisting force, and rejoining the two strands
DNA polymerase III
main replication enzyme in E.Coli; extends the RNA primer by adding DNA nucleotides to it
DNA polymerase I
E.coli enzyme that uses it 5’ to 3’ exonuclease activity to remove the RNA of the previously synthesized Okazaki fragment, and uses its 5’ to 3’ polymerization activity to replace the RNA nucleotides with DNA nucleotides
Sliding Clamp
tethers DNA polymerase III to the DNA template, making replication more efficient
DNA synthesis
- begins at sites that act as replication origins
- only activated once during S phase
- proceeds from the origins as two replication forks moving in opposite directions
Telomeres
- the ends of eukaryotic chromosomes
- short sequences repeated hundreds to thousands of times
- protects against chromosome shortening during replication
Telomerase
enzyme that prevents chromosome shortening by adding telomere repeats
Proofreading
if a replication error causes a base to be mispaired, DNA polymerase reverses and removes the most recently added base
-the enzyme then resumes DNA synthesis in the forward direction
DNA repair mechanisms
- Recognize
- Remove
- Resynthesize