DNA: Genetic Material
Overview
History of DNA
DNA Structure
DNA Replication
Eukaryotic Replication
DNA Repair
Frederick Griffith
In 1928, Frederick Griffith was working on a
vaccine for the flu
At that time, they thought the cause of
the flu was a bacteria called
Streptococcus pneumoniae
During his experiment he got some
unforeseen results
There existed two strains of S. pneumoniae
S form: which was virulent and causes pneumonia
R form: non virulent, does nothing
S: Virulent R: Safe S: Virulent S: Virulent R: Safe
Griffith Experiment
Somehow the information for virulence that was
in the dead s type bacteria had passed on to the
live R type.
This transfer of information is called transformation
Bacteria pick up DNA and incorporate it into their
DNA
Avery, MacLeod, & McCarty
Experiment
They prepared samples of Griffith’s heat killed S-Strains
and added them to different enzyme solutions
The enzyme solutions would break down specific
biomolecules
Dnase – breaks down DNA
Proteinase – breaks down proteins
Rnase – breaks down RNA
And others
They added the R strain like in Griffith’s experiment and
observed which would transformation
The Hershey and Chase Experiment
During this time, many scientists believed that
proteins were in charge of storing heredity
Hershey and Chase wanted to test this idea
They used a bacteriophage
Virus that only consists of DNA and a protein Coat
Two Experiments were held
DNA Structure
Once it was learned that genes were
made up of DNA, the structure of the DNA
became the next big wonder
The science community knew DNA was
made up of nitrogen bases
The purines: Adenine and Guanine
The pyrimidines: Thymine and Cytosine
Erwin Chargaff
Decided to analyze in detail the DNA of many
different species
He found that each species had different amounts of
A, T, G and C
Each species had equal amounts A = T and G = C.
For humans, we had 31% A and T and 19% G and C
His data suggested that DNA has a means to be
stable, where A can only pair with T and G can only
pair with C
Also that DNA can be variable for genetic material
Rosalind Franklin
Studied DNA using X-
ray crystallography
Her data showed
DNA to be a helix with
some portions
repeating over and
over
Types of Possible DNA Replication
There were 3 Models of replication at this time
Conservative Model: Parent Strands of DNA will still
be intact and new copies will be in the new strands
Semiconservative: Daughter strands will consist of
one parent and one new strand
Dispersive: New and old DNA is dispersed
throughout each strand of both daughter
molecules
Jump to long image description
Meselson and Stahl
Nitrogen is important for DNA replication
They grew bacterial cells in an isotope of
Nitrogen (Nitrogen 15) for many generations
After several generations, the DNA was denser
than normal DNA because of Nitrogen 15
isotope
The sample was then switched back to Nitrogen
14 and DNA samples were extracted from the
cells at different generations
Watson and Crick Model
Worked together to create a model for
DNA
Based on the previous experiments, they
knew
DNA contains 4 types of nucleotides with
bases A, T, G, and C
Amount of A = T and G = C
DNA is a double helix with repeating patterns
Watson and Crick’s Model
Created a twisting model
of DNA
Model suggested how
replication works
The model mostly holds
true today, a few
changes
They won the Nobel Prize
DNA Structure
DNA is a double helix, like a twisted ladder
Both strands run ANTI Parallel, meaning they run in opposite directions
Composed of nucleotides
5-carbon sugar called deoxyribose.
Phosphate group (PO4).
Attached to 5′ carbon of sugar.
Nitrogenous base.
Adenine, thymine, cytosine, guanine.
Free hydroxyl group (—OH).
Attached at the 3′ carbon of sugar.
Nucleotide subunits of DNA and RNA
Access the text alternative for slide images
© 2020 McGraw-Hill Education. 14-22
Phosphodiester bond
Bond between adjacent
nucleotides
Formed between the phosphate
group of one nucleotide and the 3′
—OH of the next nucleotide
The chain of nucleotides has a 5′-
to-3′ orientation
© 2020 McGraw-Hill Education. 14-23
Figure 11.5 DNA structure. Copyright © The McG raw-Hill Compan ies, In c. Permission re quired for repro duction or display.
C P
sugar-pho sph ate
G
C backbone
P
G
T
A P
P
A
T
P complementary
hydrog en base pairin g P
bon d
OH G
P
2' 3'
5' T
A C
S 1' 1' S 4'
4' P
3' 2' 5' P
3' end 5'end P
C
OH 5' end
a. Nucleotide pair
P G
hydrog en bonds
sugar
OH 3' end
b. Str ucture of DNA
DNA Replication
Process of copying DNA
DNA unravels, and each strand is used as a
template for the new strands
Since each new DNA molecule is made of one
parent strand, this is known to be
SEMICONSERVATIVE
DNA Replication DNA Polymerase only moves
5 prime to 3 prime
So it is a little more difficult on the
Other Strand
RNA DNA Helicase
RNA Primase
PolymeraseDNA Splits the strand of DNA
Ligase
Notice the Gap
That needs to be fixed
We need to fuse these patches of
Okazaki Fragments
RNA
Primase
DNA
Polymerase
Now it is time to create the
New To start with
strand the replication
Don’t Forget DNA Polymerase
RNA Primase comes in
Both Strands Run ANTIPARALLEL
RNA Structure
Ribonucleic Acid (RNA)
Contains sugar ribose
Base Pairs are A, C, G, and Uracil (not thymine)
Single stranded
3 types
Messenger RNA (mRNA) – used for protein synthesis
Transfer RNA (tRNA) transfers amino acids from
cytoplasm to ribosomes
Ribosomal RNA (rRNA) – creates ribosomes
Figure 11.8 Structure of RNA.
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
P
S Based in uracil
U
instead of thymine
P
S
A
G P
S C
U
A P
one S
C
nucleotide ribose
DNA Repair
DNA can become damaged by multiple different ways
UV Light, X rays, chemicals in the environment
Factors that increase the number of mutations above regular
levels of mutation are called Mutagens
DNA can be repaired usually by two different ways
Specific Repair mechanisms
Nonspecific Repair mechanisms
Photorepair: Specific repair
mechanism
When UV light hits DNA,
the strand can misshapen
in areas that have two
Thymine bases near each
other
These is called thymine
dimers
An enzyme called photolyase
uses light energy to break the
thymine dimer
Excision Repair: Nonspecific Repair
Mechanisms
A damaged region is simply excised or removed and is
then replaced
Works on 3 steps:
Recognition of damage
Removal
Resynthesis of template using other strand
Telomeres and Telomerase
There are specialized structures
on the ends of chromosomes
called telomeres
These structures protect and
maintain the integrity of the
chromosome
Consist of many short repeated
segments of DNA
Telomerase: is the enzyme that
creates and lengthens the
telomeres
Telomerase and Age
During embryonic and childhood development,
telomerase is in high activity
However, as we age, telomerase activity drops
When the telomeres shorten, the protection of
the chromosome slowly drops as well
Eventually it would lead to the non-viability of
the offspring due to the chromosomes being
damaged