dna replication packet #43 chapter #16 tuesday, october 13, 20151
TRANSCRIPT
DNA Replication
Packet #43Chapter #16
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Historical Facts About DNA
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Historical DNA Discoveries 1928
Federick Griffith finds a substance in heat-killed bacteria that “transforms” living bacteria
1944 Oswald Avery, Cloin MacLeod and Maclyn McCarty
chemically identify Griffith’s transforming principle as DNA
1949 Erwin Chargaff reports relationships among DNA bases
that provide a clue to the structure of DNA 1953
Alfred Hersey and Martha Chase demonstrate that DNA , not protein, is involved in viral reproduction.
1953 Rosalind Franklin produces an x-ray diffraction image of
DNA
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Historical DNA Discoveries II 1953
James Watson and Francis Crick propose a model of the structure of DNA.
1958 Matthew Meselson and Franklin Stahl demonstrate that
DNA replication is semi conservative replication 1962
James Watson, Francis Crick and Maurice Wilkins are awarded the Nobel Prize in Medicine for discoveries about the molecular structure of nucleic acids.
1969 Alfred Hershey is awarded the Nobel Prize in Medicine
for discovering the replication mechanism and genetic structure of viruses
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Griffith Experiment
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The Griffith experiment, conducted in 1928, was one of the first experiments suggesting that bacteria are capable of transferring genetic information through a process known as transformation.
Hershey Chase Experiment
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Hershey and Chase conduced an experiment using viral DNA to show that the DNA was the genetic material being inserted into the bacteria and used to replicate more viruses.
Structure of DNA
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Introduction I
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DNA is an organic macromolecule known as a nucleic acid.
Nucleic Acids are composed of building blocks known as nucleotides.
Nucleotides have three parts: - Phosphate Sugar Nitrogenous bases
DNA Nucleotides Multiple DNA nucleotide subunits link together
to form a single DNA strand. DNA nucleotides are composed of: -
Phosphate Sugar
Deoxyribose Nitrogenous Bases
Purines (Two Rings) Adenine Guanine
Pyrimidines (One Ring) Thymine Cytosine
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DNA Nucleotides II
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Nucleotides are linked together by covalent phosphodiester bonds
Each phosphate attaches to the 5’ end (carbon #5) of one deoxyribose and to the 3’ end (carbon #3) of the neighboring deoxyribose Makes up the sugar-
phosphate backbone
DNA Strands
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Each DNA strand, that is composed of multiple nucleotides, has a head and a tail. Head = 5’ end
Phosphate group Tail = 3’ end
Hydroxyl group
DNA Molecule
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Each DNA molecule consists of two DNA strands (polynucleotide chains) that associate as a double helix
The two strands/chains run antiparallel
Base-Pairing Rules for DNAChargaff Rules
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The two DNA strands are joined together at the nitrogenous bases.
Holding the bases together, and allowing the formation of the double helix, are hydrogen bonds.
Base-Pairing Rules for DNAChargaff Rules II
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Adenine forms two hydrogen bonds with thymine
Guanine forms three hydrogen bonds with cytosine These pairings are
known as Chargaff’s rules A always pairs with T G always pairs with C
Complementary base pairing
Chargaff Rules III
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Models of DNA Replication
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Models of DNA Replication
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There were three models proposed about how DNA replicates.
However, the one that stood the test was semi-conservative replication.
DNA Replication Introduction
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In semi-conservative replication, each “old” strand of DNA is used to create a new complementary strand.
Introduction to DNA Replication
The Players
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Introduction to the Strands
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Template Strands {The Parental Strands} Are the strands
being copied The original DNA
strands During DNA
replication, both strands are copied This means that there
are TWO template strands
Introduction to the Strands II
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Complementary Strands {The Daughter Strands} The NEW DNA strands
produced from the Template Strands
During DNA replication, there are TWO complementary strands Always remember that
the process started with TWO template strands
Origin of Replication & Bi-directionality.
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DNA replication is bidirectional and starts at the origin of replication The process proceeds
in both directions from that point.
A eukaryotic chromosome may have multiple origins of replication Allows the process to
occur faster and more efficient
Introduction to the Making of the Complementary Strand.
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DNA replication/synthesis, of the complementary strands, proceed in a 5’ to 3’ direction. Nucleotides can ONLY
be added to the 3’ end.
Introduction to the Making of the Complementary Strand.
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Since DNA nucleotides can only be added to the 3’ end, it causes one of the complementary strands to be produced continuously and the other discontinuous The continuous strand is
called the leading strand The discontinuous strand
is called the lagging strand Is first synthesized as
short Okazaki fragments before becoming one strand
Enzymes of DNA Replication & The Steps of DNA Replication
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Enzymes of DNA Replication
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Helicase Unzips DNA double-helix
Topoisomerases Prevents tangling and
knotting of DNA as the while the strands are unzipped.
RNA primase Initiates the formation of
“daughter” strands Forms a segment known
as the RNA primer The RNA primer contains
the nitrogenous base Uracil
Enzymes of DNA Replication II
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DNA Polymerase III Enzyme that catalyzes the
polymerization (making) of nucleotides
Adds Deoxyribonucleotides (nucleotides only found in DNA, as opposed to RNA) to the 3’ end of a growing nucleotide chain
Acts at the replication fork DNA Polymerase I
A type of DNA polymerase will change the RNA primers into DNA Changing the base Uracil
into Thymine
Enzymes of DNA Replication III
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DNA Ligase Enzyme responsible
for joining Okazaki fragments forming the Lagging Strand
Gyrase Returns the DNA
strands into a Double Helix
Zips the DNA back together
DNA Replication—The Big Picture
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DNA Replication—Lagging Strand
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Post DNA Replication
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DNA Excision RepairDNA Polymerase II
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On some occasions, errors in nucleotides may occur while making the new DNA strand. Errors such as
mismatches & dimers may occur.
To correct these errors, the enzymes nuclease, DNA polymerase III and DNA ligase are used during the process known as excision repair.
Telomeres, Telomerase & DNA Shortening
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At the end of eukaryotic chromosomes are known as telomeres Short, repetitive DNA
sequences that do not contain genes. Typically 100 to 1000
nucleotides TTAGGG (Humans)
Telomeres help protect the organism's genes from being eroded through successive rounds of DNA replication.
Telomeres, Telomerase & DNA Shortening
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Telomeres shorten each cell cycle (DNA replication sequence) but can be extended using the enzyme telomerase Absence of telomerase in
certain cells may be the cause of “cell aging” Cells having a limited
number of cell divisions Most cancer cells have
telomerase to maintain the telomeres and possibly resist apoptosis.