ch 6 Flashcards
(26 cards)
Griffith’s Transformation Experiment (1928):
Studied Streptococcus pneumoniae bacteria.
Found that heat-killed virulent (smooth, S) strain could
ransfer genetic material to the non-virulent (rough, R) strain
Nucleotides are the building blocks of DNA, consisting of:
phosphate group.
A deoxyribose sugar.
A nitrogenous base (A, T, C, G).
Chargaff’s Rule:
A = T, C = G (Base pairing follows a 1:1 ratio).
Nucleotides Link via
Phosphodiester Bonds:
Covalent bonds form between the phosphate of one nucleotide and the sugar of the next.
Avery, MacLeod, and McCarty (1944):
Showed that DNA, not protein or RNA, was the “transforming principle” by selectively destroying DNA, RNA, and proteins and testing for transformation.
Hershey-Chase Experiment (1952):
Found that only DNA entered the bacterial cells, proving it was the genetic material.
A-T pairs form
2 hydrogen bonds.
C-G pairs form
3 hydrogen bonds (stronger bond).
Double Helix Model
Antiparallel Strands:
One strand runs 5’ → 3’, the other 3’ → 5’.
Major Steps in Recombination
Double-Strand Break Formation –
End Processing –
Strand Invasion –
DNA Synthesis –
Holliday Junction Formation –
Resolution –
Double-Strand Break Formation –
Enzymes cut the DNA.
End Processing
The ends of the broken strands are trimmed.
Strand Invasion –
One strand invades the homologous chromosome, forming a D-loop
DNA Synthesis –
NA polymerase extends the invaded strand.
Holliday Junction Formation –
he structure allowing crossover.
Resolution –
holliday junction is cut in different ways, leading to crossover or non-crossover products.
Only non-sister chromatids of homologous chromosomes participate in
dna steps
Each new DNA molecule consists of
one original (parent) strand and one newly synthesized strand.
DNA polymerase adds nucleotides only to the 3’ end,
making replication occur 5’ → 3’.
Origin of replication is
y specific DNA sequences recognized by a protein complex called the Origin Recognition Complex (ORC)
Steps of DNA Replication
Initiation:
Origin of replication is identified.
Helicase unwinds DNA.
Primase synthesizes RNA primers.
Elongation:
DNA polymerase adds nucleotides 5’ → 3’.
Leading strand: Continuous synthesis.
Lagging strand: Synthesized in short Okazaki fragments.
Polishing (Termination & Proofreading):
Exonucleases remove primers.
DNA Ligase joins Okazaki fragments.