Ch 16 DNA the Central Dogma history structure

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Ch. 16 DNA: the Central Dogma, history, structure Replication

Ch. 16 DNA: the Central Dogma, history, structure Replication

History: timeline, people and their accomplishments n n n Mendel (heredity) Sutton Chromosomes Thomas

History: timeline, people and their accomplishments n n n Mendel (heredity) Sutton Chromosomes Thomas Hunt Morgan (flies, linkage) Griffith (1928) transformation and mice Avery and colleagues (1944): n n Chargaff (late 40’s-early 50’s) n n proposed DNA as the transforming agent base pairing (AT CG) Hershey-Chase (1952) DNA IS hereditary material Watson and Crick (1953) (Franklin) chemical structure of DNA Meselson-Stahl mid 1950’s n DNA Replication details

Griffith: Transformation

Griffith: Transformation

Hershey / Chase (the hereditary material is not a protein) Radioactive P and S

Hershey / Chase (the hereditary material is not a protein) Radioactive P and S

Whose rule? Purine? Pyrimidine? You have 6 billion pair in every cell! A-T C-G

Whose rule? Purine? Pyrimidine? You have 6 billion pair in every cell! A-T C-G

Chargaff’s Rule Purines (A, G, double rings) always pair with Pyrimidines (T, C, single

Chargaff’s Rule Purines (A, G, double rings) always pair with Pyrimidines (T, C, single rings) n A-T, C-G (& in RNA? ____) n Old AP test question: if in a cell the DNA bases are 17% A’s then what are the %’s of the other bases? n n CUT your PY or Pure Silver (Ag)

DNA Replication: SEMICONSERVATIVE MODEL How did they (Meselson-Stahl) prove this? FIG 16. 8

DNA Replication: SEMICONSERVATIVE MODEL How did they (Meselson-Stahl) prove this? FIG 16. 8

KNOW: Steps of Replication Enzymes Leading and Lagging strands Okazaki Fragments Anti-parallel Video

KNOW: Steps of Replication Enzymes Leading and Lagging strands Okazaki Fragments Anti-parallel Video

“Bubbles” Replication forks, simultaneous replication **Eukaryotes - multiple origins of replication Semi-conservative This process

“Bubbles” Replication forks, simultaneous replication **Eukaryotes - multiple origins of replication Semi-conservative This process is fueled by… nucleoside triphosphates **Prokaryotes have one

DNA is made from 5’ to 3’ and it is read from 3’-5’. The

DNA is made from 5’ to 3’ and it is read from 3’-5’. The 3’ end is the end which elongates (grows) Why is this direction important to consider in Replication?

What do the terms 5’ and 3’ mean?

What do the terms 5’ and 3’ mean?

Leading & Lagging strands, made 5’-3’ Okazaki fragments (are of the lagging strand) ENZYMES:

Leading & Lagging strands, made 5’-3’ Okazaki fragments (are of the lagging strand) ENZYMES: helicase, DNA Polymerase, ligase

Enzymes : • Helicase • Single strand binding proteins • Primase (RNA Primer) •

Enzymes : • Helicase • Single strand binding proteins • Primase (RNA Primer) • DNA Polymerase • Ligase • Nuclease and DNA Polymerase (both are repair enzymes)

Let’s see this in Action n n Leading Strand (Nobelprize. org) Lagging Strand (Nobelprize.

Let’s see this in Action n n Leading Strand (Nobelprize. org) Lagging Strand (Nobelprize. org) Overall (wiley) Overall 3 D view (wehi. edu. au or dnai. org) (Youtube has a music version)

Telomeres Unfilled gap left at the ends of the DNA strands due to the

Telomeres Unfilled gap left at the ends of the DNA strands due to the use of RNA primers Eventual shortening of DNA over time

Enzyme: Telomerase extends the (3’) long strand so the 5’ strand can finish. Telomerase

Enzyme: Telomerase extends the (3’) long strand so the 5’ strand can finish. Telomerase is found in germ cells that give rise to gametes.

How’s it all fit? n DNA coiling – Let’s see it! DNA from a

How’s it all fit? n DNA coiling – Let’s see it! DNA from a single skin cell, if straightened out, would be about six feet long but invisible. Half a gram of DNA, uncoiled, would stretch to the sun. Again, you couldn't see it.