The Molecular Basis of Inheritance

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Presentation transcript:

The Molecular Basis of Inheritance Chapter 16

Searching for Genetic Material, I Mendel: modes of heredity in pea plants Morgan: genes located on chromosomes Griffith: bacterial work; transformation: change in genotype and phenotype due to assimilation of external substance (DNA) by a cell Avery: transformation agent was DNA

Searching for Genetic Material, II Hershey and Chase √ bacteriophages (phages) √ DNA, not protein, is the hereditary material √ Experiment: sulfur(S) is in protein, phosphorus (P) is in DNA; only P was found in host cell

DNA Structure Chargaff (1950)  ratio of nucleotide bases (A=T; C≈G) Watson & Crick (1953)  (Wilkins, Franklin)  The Double Helix  nucleotides: nitrogenous base (thymine, adenine, cytosine, guanine); sugar deoxyribose; phosphate group

DNA Bonding Purines: A & G Pyrimidines: C & T (Chargaff rules) 2 hydrogen bonds between A-T and 3 hydrogen bonds between C-G How did they know?

DNA Structure Van der Waals attractions between the stacked pairs help hold the molecule together

DNA Replication Watson & Crick strands are complementary; nucleotides line up on template according to base pair rules (Watson)

DNA Replication: a closer look Origin of replication (“bubbles”): beginning of replication Replication fork: ‘Y’-shaped region where new strands of DNA are elongating Helicase: catalyzes the untwisting of the DNA at the replication fork DNA polymerase: catalyzes the elongation of new DNA

DNA Replication, II Antiparallel nature: sugar/phosphate backbone runs in opposite directions (Crick); one strand runs 5’ to 3’, while the other runs 3’ to 5’; DNA polymerase only adds nucleotides at the free 3’ end, forming new DNA strands in the 5’ to 3’ direction only

DNA Replication, III Leading strand: synthesis toward the replication fork (only in a 5’ to 3’ direction from the 3’ to 5’ master strand) Lagging strand: synthesis away from the replication fork (Okazaki fragments); joined by DNA ligase (must wait for 3’ end to open; again in a 5’ to 3’ direction) Initiation: Primer (short RNA sequence~w/primase enzyme), begins the replication process

DNA Repair Mismatch repair: DNA polymerase Excision repair: Nuclease Telomere ends: telomerase