DNA Replication Nucleotides Transformation Griffith 1928 T H

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DNA Replication

DNA Replication

Nucleotides

Nucleotides

Transformation (Griffith 1928)

Transformation (Griffith 1928)

T. H. Morgan Genes are located on chromosomes

T. H. Morgan Genes are located on chromosomes

Avery, Mc. Carty, Mac. Leod (1944) Genetic Material Protein or DNA ? ? "Studies

Avery, Mc. Carty, Mac. Leod (1944) Genetic Material Protein or DNA ? ? "Studies on the chemical nature of the substance inducing transformation of pneumococcal types"

Phages

Phages

Hershey & Chase (1952)

Hershey & Chase (1952)

Linus Pauling (1948) Alpha Helix Structure

Linus Pauling (1948) Alpha Helix Structure

Chargaff’s Rule Adenine – Thymine Guanine - Cytosine

Chargaff’s Rule Adenine – Thymine Guanine - Cytosine

Watson & Crick

Watson & Crick

Maurice Wilkins X-ray diffraction

Maurice Wilkins X-ray diffraction

Rosalind Franklin

Rosalind Franklin

Nucleotides

Nucleotides

X-ray Data

X-ray Data

DNA Structure

DNA Structure

Complimentary Strands

Complimentary Strands

Semiconservative Model (Meselson & Stahl)

Semiconservative Model (Meselson & Stahl)

Semiconservative Model (Meselson & Stahl)

Semiconservative Model (Meselson & Stahl)

Origin of Replication

Origin of Replication

DNA Nucleosides Triphosphates

DNA Nucleosides Triphosphates

Antiparallel

Antiparallel

Enzymes DNA Polymerase Helicase Single-strand binding protein Topoisomerase RNA primase Ligase

Enzymes DNA Polymerase Helicase Single-strand binding protein Topoisomerase RNA primase Ligase

RNA Primer Uses RNA primase to build RNA primer Eventually replaced with DNA by

RNA Primer Uses RNA primase to build RNA primer Eventually replaced with DNA by DNA Polymerase

DNA Replication

DNA Replication

Leading and Lagging Strands Leading Strand Built in the 5’-3’ direction Built toward the

Leading and Lagging Strands Leading Strand Built in the 5’-3’ direction Built toward the replication fork Built continuously Uses one RNA Primer Lagging Strand Built in the 5’-3’ direction Built away from the replication fork Built discontinuously using Okazaki fragments Many RNA Primers

Overview

Overview

Proofreading Mismatch Repair Nucleotide Excision Repair (nucleases)

Proofreading Mismatch Repair Nucleotide Excision Repair (nucleases)

End-replication Problem Nucleotides can only be added to 3’ end Leaves gap on leading

End-replication Problem Nucleotides can only be added to 3’ end Leaves gap on leading strand Each replication causes DNA molecule to get smaller

Telomeres

Telomeres

Telomeres End of DNA strand made up of reoccurring DNA sequence Can be rebuilt

Telomeres End of DNA strand made up of reoccurring DNA sequence Can be rebuilt with telomerase (only in germ-line cells)