Transcript File

MUTATIONS
Mutations


errors/changes in the DNA sequence that are
inherited.
May have a negative effect, a positive effect, or no
effect.
Negative Effect
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Example: cystic fibrosis
A particular membrane protein (chloride channel)
transports chlorine ions between the cell and the
extracellular fluid
A mutation in the gene for the protein results in the
absence or defective chloride channels
Positive effects
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Organisms have evolved as a result of mutations
that have been naturally selected for.
Example: The large size human brain arose from a
series of mutations
No effect

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Sometimes the mutation doesn’t change the fitness
(survival) of an organism.
Ex: Eye colours
Sometimes the side effect of a mutation may not be
seen immediately (either later in the lifespan of the
organism or in another generation under particular
environmental conditions)


Ex: Huntington’s Disease (degenerative nervous
system disease) isn’t noticeable until 35-40 years of
age.
Viruses: The reason why the influenza virus comes
back every year is because it keeps mutating.


Diploid chromosomes have 2 copies of each gene
(one on each chromosome – 1 which came from
your mom, the other from your dad)
If there is an error in one copy, the other may
compensate
Types of Mutations

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Point Mutations
Chromosomal Mutations
POINT MUTATIONS
Mutations at a specific base pair in the genome
 Include:
silent mutations
missence mutations
- substitution
- deletion
- addition/insertion
frameshift mutations
- deletion
- addition/insertion

Silent Mutation

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Does not result in a change in the amino acid coded
for by the mRNA transcript
Therefore, does not cause any visible changes in the
organism
Ex: If a mutation occurs in the intron sequence, it will
be removed from the mRNA strand before the
protein is even translated

Ex:
Codes for the amino acid phenylalanine
proper mRNA sequence
mutated sequence
5’ AGG CUG UUU GGA 3’
5’ AGG CUG UUC GGA 3’
Still codes for the amino
acid phenylalanine

If there is a mistake in the original DNA sequence or in
the transcription of the mRNA strand, the mutation
may go unnoticed because there is often multiple
codons for the same amino acid
Missense Mutation


A change in the base sequence that alters a codon,
resulting in a different amino acid being placed in
the protein chain
Ex: Sickle Cell Anaemia
Nonsense Mutation
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A change in the base sequence that converts a
codon for a particular amino acid into a stop codon.
Therefore, the translation of the protein will stop
prematurely
The protein fragment produced from this mutation
are shorter than the protein originally coded for and
they may be broken down by proteases in the cell
These mutations are often lethal to the cell

Missense and Nonsense mutations may be caused
by:
 Substitution
 Deletion
 Insertion
Substitution

The replacement of one base in a DNA sequence by
another base.
(Substitution could also lead to a silent mutation as in
the example before)
Missense Mutation
proper mRNA sequence
mutated sequence
phenylalanine
5’ AGG CUG UUU GGA 3’
5’ AGG CUG UUA GGA 3’
leucine
The “mutant” sequence may make a completely functional protein, a defective
protein (but still functional protein), or a completely non-functional protein,
Nonsense Mutation
Proper mRNA sequence
mutated sequence
leucine
5’ AGG CUG UUA GGA 3’
5’ AGG CUG UAA GGA 3’
Stop codon
Deletion

One or more nucleotides is removed from the DNA
sequence.
Normal mRNA
AUG GGA UUC AAC GGA AUA
Met - Gly - Phe - Asn - Gly - Ile
mRNA with Deletion
AUG GAU UCA ACG GAA UA
Met – Asn – Leu – Thr - Gln

Creates a drastic change that most likely yields a defective
protein
Insertion (or Addition)

The addition of an extra nucleotide in the DNA
sequence.
Normal mRNA
AUG GGA UUC AAC GGA AUA
Met - Gly - Phe - Asn - Gly - Ile
mRNA with Insertion
AUG GGA AUU CAA CGG AAU A
Met – Gly – Ile – Gln - Arg - Asn 
Creates a drastic change that is most likely yields a defective
protein
Frameshift Mutations
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The previous 2 examples of deletion and insertion
resulted in a change to the reading frame called a
frameshift mutation.
This drastically changes the protein, causing pretty
much every amino acid after the mutation to be
incorrect
Therefore, frameshift mutations will most likely create
a defective, non-functioning protein
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A deletion or insertion of 1 or 2 nucleotides leads to
frameshift mutations.
The deletion or insertion of 3 nucleotides does NOT
shift the reading frame. It will result in the removal
or addition of 1 amino acid only.
This may change the overall protein shape, but may
not have as serious an impact as a frame shift
mutation
What type of mutation?
SUBSTITUTION causing a SILENT MUTATION
What type of mutation?
SUBSTITUTION causing a MISSENSE MUTATION
What type of mutation?
SUBSTITUTION causing a NONSENSE MUTATION
What type of mutation?
DELETION causing a FRAMESHIFT MUTATION
(and extensive missense mutation)
What type of mutation?
INSERTION causing a FRAMESHIFT MUTATION
(and an immediate NONSENSE MUTATION)
What type of mutation?
DELETION of 3 nucleotides- no frameshifting
Chromosomal Mutations

Mutations of large segments of DNA on the
chromosome
Recall….
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In prophase I of Meiosis, homologous chromosomes
pair up and crossing over may occur.
TRANSLOCATION

Fragments of DNA from 2 different (nonhomologous
chromosomes) exchange places
Translocation
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Happens when two non-homologous chromosomes
interact
Disrupts the normal structure of the genes
When the chromosome is transcribed, the 2
unrelated sequences on a single chromosome will
create a new protein with altered function.
Known to cause some types of leukemia
Transposable Elements

Happens within one chromosome

“jumping genes”

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Fragments of DNA that consistently move from
location to location on a chromosome.
If it lands in a coding region of a gene, it will
disrupt the transcription of a gene
Inversion

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The reversal of a segment of DNA within a single
chromosome
Genetic material not gained or lost
However, may disrupt a gene sequence.
Causes of Mutations

Spontaneous Mutations
 Not
caused by environmental conditions;
 Errors made in DNA replication
 ex: accidentally inserting an incorrect base.
Causes of Mutations

Induced Mutations
 Mutations
caused by a chemical agent or radiation
 Could lead to certain cancers ie: melanoma (skin cancer)
These induced mutations are caused by Mutagenic
agents
 Agents
that can cause a mutation
 Ex: UV radiation, X rays, certain chemicals (pesticides)