Ch. 16 DNA

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

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Ch. 16 DNA. DNA: the Central Dogma, history, structure Replication. History: timeline, people and their accomplishments. Mendel (heredity) Sutton Chromosomes Thomas Hunt Morgan (flies, linkage) Griffith (1928) transformation and mice Avery and colleagues (1944): - PowerPoint PPT Presentation

Transcript of Ch. 16 DNA

Page 1: Ch. 16 DNA

Ch. 16DNA

DNA: the Central Dogma, history, structure

Replication

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History: timeline, people and their accomplishments

Mendel (heredity) Sutton Chromosomes Thomas Hunt Morgan (flies, linkage) Griffith (1928) transformation and mice Avery and colleagues (1944):

proposed DNA as the transforming agent Chargaff (late 40’s-early 50’s)

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

DNA Replication details

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Griffith: Transformation

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Hershey / Chase (the hereditary material is not a protein)

Radio-active P and S

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Whose rule? A-T C-G

Purine? Pyrimidine?You have 6 billion pair

in every cell!

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Chargaff’s Rule Purines (A, G, double rings) always pair

with Pyrimidines (T, C, single rings) A-T, C-G (& in RNA? ____) Old AP test question: if in a cell the

DNA bases are 17% A’s then what are the %’s of the other bases?

CUT your PY or Pure Silver (Ag)

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DNA Replication:

SEMICONSERVATIVE MODEL

How did they (Meselson-Stahl) prove this? FIG 16.8

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KNOW: Steps of ReplicationEnzymesLeading and Lagging strands Okazaki FragmentsAnti-parallel

Video

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This process is fueled by…nucleoside nucleoside triphosphatestriphosphates

Semi-conservative

“Bubbles”

Replication forks,

simultaneous replication

**Eukaryotes - multiple

origins of replication

**Prokaryotes have one

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

The 3’ end is the end which elongates (grows)

Why is this direction important to consider in Replication?

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What do the terms 5’ and 3’ mean?What do the terms 5’ and 3’ mean?

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Leading & Lagging strands, made 5’-3’

Okazaki Okazaki fragmentsfragments (are (are of the lagging of the lagging

strand)strand)ENZYMES: helicase, DNA Polymerase, ligase

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Enzymes :Enzymes :•Helicase

•Single strand binding proteins•Primase (RNA Primer)•DNA Polymerase•Ligase

•Nuclease and DNA Polymerase (both are repair enzymes)

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Let’s see this in Action Leading Strand

(Nobelprize.org) Lagging Strand

(Nobelprize.org) Overall

(wiley) Overall 3D view

(wehi.edu.au or dnai.org)(Youtube has a music version)

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

Eventual shortening of DNA over time

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

Telomerase is found in germ cells that give rise to gametes.

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How’s it all fit?

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.