Transcript Mutations
MUTATIONS
1. Silent Mutations
Change in nucleotide has no effect on amino
acid in protein
Occurs:
Introns
Wobble effect
Intron Mutations
Variable effects
Intron Mutations
m1: Mutations in the promoter region may affect gene transcription may lead to nonfunctional (null) alleles.
m2: Mutations in exons, if they result in the substitution of an amino acid in the active
site or other critical region of the protein, also lead to alleles with modified (reduced)
functionality.
m3: In contrast, exon mutations that result in changes outside the active sites or at 3rd
codon positions may have little or no effect on gene function.
These mutations are called silent (if the amino acid is unchanged) or neutral (if
the change has no effect).
m4: Mutations at critical positions near intron / exon junctions may affect mRNA
splicing and lead to the deletion or retention of entire exons, and result in null alleles.
m5: Mutations that occur in non-coding introns, or
m6: 5' or 3' flanking portions of the gene, may have little or no effect on gene
function. able effects
2. Missense Mutations
Change in DNA base sequence alters a codon
A different amino acid is added to protein
Examples:
Sickle Cell Anemia
Hemophilia
Sickle Cell Anemia
GAA GUA
GLU VAL
Haemophilia
Sex-linked (X-chromosome) disorder that
impairs blood clotting
Dominant in males, recessive in females
Used to stop bleeding when a vessel breaks
1 in 5,000-10,000
G A
GLU LYS
*Affecting the protein necessary for blood clotting
3. Nonsense Mutations
Change in DNA base sequence causes a stop
codon to replace a normal codon
Lethal to cell as protein function is lost
DEPENDING ON where the stop codon is
If occurs at beginning of protein sequence lethal
If occurs at end of protein sequence may lose
function
Example: Thalassemia and DMD
Thalassemia
Mutation that reduces the rate at which one protein in
hemoglobin (Hb) is synthesized
Creating incomplete or abnormal Hb lower function
AAG UAG at the 57 codon of the gene
LYS STOP
DMD = Duchenne Musclar Dystrophy
X-linked trait that causes rapid deterioration of
muscles
Loss of motion, then eventual death
Affects in 1 in 3500 males
Females only affected if both parents have allele
C A G or C A A U A G or U A A
GLN STOP
DMD = Duchenne Musclar Dystrophy
Dystrophin protein no longer functions properly
Responsible for connecting muscle fibers to the basal layer
of skin
Absence of dystrophin permits excess Ca2+ to enter
the cell
Eventually cell is destroyed from oxidative processes
4. Frameshift Mutations
Change in DNA base sequence causes the
reading frame of codon to change due to:
Insertion of base(s)
Deletion of base(s)
*INDEL mutations
Single or double INDEL will cause an amino acid
change
Triplet INDEL will have milder consequences
Multiple triplet INDEL can have major effects
Ex. Fragile X, Cystic Fibrosis
Fragile X
Associated with:
Martin-Bell Syndrome, the most common form
of inherited predisposition to mental retardation
Protein FMR1 is not made
Required for normal neural development
Characterized by high amounts of CGG triplet
repeats
Fragile X
Cystic Fibrosis
Recessive disease that causes progressive body wide
disability
First recognized in the early 1930s
Scarring of the pancreas
Early death ~35 years old
Symptoms (few of the many):
Difficulty breathing (from lung infections)
Poor growth
Diarrhea
Infertility
1 in 25 people of European descent
Cystic Fibrosis
Caused by a mutation in the gene for the protein CFTR
Regulates sweat, digestion processes, and mucus
3 base pairs are deleted
Normal DNA sequence
T A G A A A A U G U U U ILE + PHE
Mutated DNA sequence
T A A A U U ILE
*ILE is still present but we lose PHE
5. Translocation
Transfer of a DNA fragment from one site to another
May get altered function depending on where it was
cut
Ex. Leukemia
Leukemia
An uncontrolled proliferation of one kind of white
blood cell (leukocyte)
All descended from a cell that lost ability to maintain cell
cycle
Translocation between chromosome 9 and 22
Chromosome 9 is longer than normal
Chromosome 22 is shorter than normal
6. Inversion
Chromosomal segment that has reversed its
orientation
No gain or loss of genetic information
But gene may be
disrupted
Protein function
loss