Title: DNA, RNA
1DNA, RNA Protein Synthesis
2Griffiths Transformation Experiment
- 1928 Frederick Griffith is studying how certain
strains of bacteria cause pneumonia and
inadvertently makes a discovery about how genetic
information is passed from organism to organism - His Experiment
- Grow two slightly different strains (types) of
bacteria - One strain proven harmless and other deadly
- Laboratory mice are injected with these strains
3Griffiths Results
4What caused Griffiths results?
- The heat-killed strain passed on its
disease-causing ability to the live harmless
strain. - In Griffiths words, one strain of bacteria was
TRANSFORMED into another. - It was later demonstrated by Oswald Avery and
other scientists that the transforming factor was
DNA (deoxyribonucleic acid)
5The Hershey-Chase Experiment
- Alfred Hershey Martha Chase studied viruses,
which are non-living particles smaller than a
cell that can infect living organisms. - Bacteriophages specific group of viruses that
infect bacteria. - OBJECTIVE To determine which part of the virus
(protein or DNA) enters a bacteria it is
infecting.
6What did Hershey Chase do?
- If Hershey and Chase could determine which part
of the virus entered an infected cell, they would
learn whether genes were made of protein or DNA. - To accomplish this, they grew viruses in cultures
containing radioactive isotopes of phosphorus-32
(32P) and sulfur-35 (35S). - Some viruses had P-32 in their DNA, and others
had S-25 in their protein coat. - If S-35 is found in the bacteria, it would mean
that viruses release their protein and if P-32 is
found in the bacteria it would mean that viruses
release their DNA.
7Recall Method of Bacteriophage Infection
- When a bacteriophage enters a bacterium, the
virus attaches to the surface of the cell and
injects its genetic information into it. - The viral genes replicate to produce many new
bacteriophages, which eventually destroy the
bacterium. - When the cell splits open, from viral overload,
hundreds of new viruses burst out and can infect
surrounding cells
8Hershey-Chase Results
So The genetic material in bacteriophages was
the DNA, (not the protein)!!!
9DNA Structure
- Made of monomers called nucleotides
- Nucleotide structure
10A nucleotide can have one of four bases
- Types of bases
- Adenine
- Guanine
- Cytosine
- Thymine
A G are bigger and are called purines C T are
smaller and are called pyrimidines
11Chargaffs Rule Rosalind Franklin
- Edwin Chargaff discovered that in almost any DNA
sample, the G nearly equals the C and the A
nearly equals the T - Rosalind Franklin used x-ray diffraction to get
information about the structure of DNA. - She aimed an X-ray beam at concentrated DNA
samples and recorded the scattering pattern of
the X-rays on film.
12Watson Crick
- Using clues from Franklins X-ray pattern, shown
to them by Maurice Wilkins, James Watson and
Francis Crick built a 3-D model that explained
how DNA carried information and could be copied. - Watson, Crick Wilkins were awarded the 1962
Nobel Prize in Physiology or Medicine for their
work.
13Base-Pairing
- Watson Crick discovered that bonds can only
form between certain base pairs, Adenine
Thymine and Cytosine Guanine. - The base-pairing rule means that purines only
pair with pyrimidines, making the rungs equally
spaced like a ladder. - The nitrogenous bases are held together by
hydrogen bonds. - A T are held together by TWO hydrogen bonds
- C G are held together by THREE hydrogen bonds
14DNA is a double-helix or twisted ladder
- The backbone or sides of the DNA molecule are
made up of alternating sugars and phosphates and
the rungs are made up of interlocking nitrogen
bases. - The sugars and the phosphates are held together
by covalent bonds and the nitrogen bases are held
together by hydrogen bonds.
15Molecular Structure of DNA
16DNA Replication
- Before a cell can divide, its DNA must be
replicated or copied in the S-phase of the cell
cycle. - In most prokaryotes, replication begins at a
single point and continues in two directions. - In eukaryotes, replication occurs in hundreds of
places simultaneously and proceeds until
complete. - Sites of replication are called replication
forks.
17How does the process occur?
- Helicase untwist DNA molecules.
- Restriction enzymes unzip the molecule.
- DNA polymerase brings in complementary base pairs
for each strand - Ligase glues together the nucleotides
- Process is semi-conservative.
- Each new strand of DNA consists of one original
template strand and one newly made strand. - This allows for proofreading, using the template
strand as the master.
18Visual Summary of DNA replication
Animation
19Replication Bubbles
20The Central Dogma of Genetics
- Genes are coded DNA instructions for the
construction of proteins. - DNA is located in the nucleus, but proteins are
made in ribosomes - To avoid damage to the DNA molecules, they are
first decoded into RNA which is sent to the
ribosome to be the instructions for protein
synthesis.
21DNA v. RNA
DNA RNA
Sugar is deoxyribose Double-stranded A, T, C G bases Sugar is ribose Single-stranded Uracil instead of thymine
22Three types of RNA
- mRNA (messenger) carries copies of instructions
for assembling amino acids into proteins - rRNA (ribosomal)
- makes up part of the ribosome
- tRNA (transfer) carries each AA
- needed to build the protein to the ribosome
23The Flow of Genetic Information
- Protein synthesis occurs in 2 steps
- transcription (DNA ? RNA) translation (RNA ?
protein)
24Transcription
- RNA is produced when RNA polymerase copies a
sequence of DNA into a complementary RNA strand. - DNA TACGGACACATT
- RNA AUGCCUGUGUAA
25Translation
- Decoding of an mRNA message into a polypeptide
chain (protein) - mRNA molecules are read in three base segments
called codons - Each codon specifies a particular amino acid
- Some AA are specified by more than one codon.
26The Genetic Code
27RNA Processing (Editing)
28Additional Details of Transcription
- Initiation RNA polymerase attached to promoter
sequence of DNA and RNA synthesis begins - 2. Elongation RNA elongates and the
synthesized RNA strand peels away from DNA
template allowing the DNA strands to come back
together in regions transcribed - 3. Termination RNA polymerase reaches
sequence of DNA bases called a terminator
signaling the end of the gene and polymerase
molecule detaches
29A Closer Look at tRNA
30A Closer Look at Ribsomes
31Steps of translation - Initiation
- After RNA is transcribed in the nucleus, it
enters the cytoplasm and attaches to a small
ribosomal subunit - special initiator tRNA binds to the start codon
bringing in the amino acid MET - large ribosomal subunit binds to the small one
creating a functional ribosome
32Steps of Translation - Elongation
- The anticodon of an incoming tRNA molecule with
AA pairs with mRNA codon in A site - AA detaches from tRNA in P site and peptide bond
forms between it and the AA in the A site - translocation P site tRNA leaves the ribosome
and the A site complex (AA, tRNA anticodon and
mRNA codon) shift s over to the P site - Process continues until a STOP codon is reached
33Steps of Translation - Termination
- Stop codons UAA, UAG, and UGA do not code for
amino acids - These codons signal the end of translation
- The completed polypeptide is released from the
last tRNA and exits the ribosome - The ribosome splits into individual subunits
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36Animation
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38Mutations
- Mutations are changes in the genetic material
- Gene Mutations change in the nucleotide
sequence within a single gene - Chromosomal mutations change in an entire
chromosome may involve loss or duplication of
multiple genes - Point mutations are gene mutations involving a
change in one or a few nucleotides - Substitution usually changes only one AA
- Frameshift addition or deletion of a nucleotide
shifts the grouping of codons
39Causes Effects of Mutations
- Causes Mutagenesis can occur in many ways
- Spontaneous mutations occur during DNA
replication or recombination - Physical or chemical agents called mutagens may
induce mutations (ex. High energy radiation from
x-rays or UV light) - Effects Can be harmful, beneficial or neither
- May cause of genetic disorders
- May be beneficial and lead to production of
proteins with new or altered activities, which
has an important role in the evolutionary process
of natural selection - Some mutations are silent and have no effect
because the nucleotide change results in a new
codon that codes for the same amino acid as the
original codon
40Substitutions Mutations
41Frameshift Mutations
424 Types of Chromosomal Mutations
Polyploidy extra set of chromosomes