Title: Mutation
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3Mutation
- A mutation is a change in the normal base pair
sequence
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Commonly used to define DNA sequence changes that
alter protein function
4Mutation
- DNA replication is extremely accurate, BUT
- Errors in polymerization occur ??????? ?????
????????? - Environmental factors, such as chemicals and
ultraviolet radiation, can alter DNA ???????
?????? ??????? ???????? - Irreversible changes to the cellular DNA can be
lethal - ??????? ?? ?????? ?????? ????? ??????
- Non-lethal changes can cause a heritable
alteration of the genetic information, called a
mutation - Genetic changes are more noticeable in germ line
cells than in somatic cells - Systems exist for the repair of damaged DNA
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7A human DNA repair defect Xeroderma pigmentosum
Multiple skin cancers due to unrepaired UV damage
to DNA
8A human DNA repair defect Bloom's syndrome
9Xeroderma pigmentosum
10Xeroderma Pigmentosum (XP) and DNA Repair Defects
- XP is an autosomal recessive disease associated
with dry skin, freckling, corneal ulceration, and
skin tumors - Many patients die before age 30 from metastases
of malignant skin tumors - One form of XP is produced by a defect in the
human endonuclease that removes pyrimidine dimers - Mutations in at least seven other genes involved
in repairing UV-damaged DNA can cause XP
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12Spontaneous mutagenesis and errors in DNA
replication
- DNA replication must accurately replicate 6 x 109
base pairs every time a human cell divides - ??? ????? ?? ?? ?????? ???? ?????? ??????????
- In man we see one new mutation per gene per
100,000 cells per cell cycle. (spontaneous
mutation frequency) - ???? ?????? ??? ??? ??? ??? ?????? ??.
13DNA polymerases have two main methods for
ensuring accuracy
(a) Base selection
Only AT and GC base pairs fit properly in the
active site of the polymerase
(b) Proofreading
If a wrong base is inserted, then it is removed
and replaced with the correct one before the next
one is added
14Induced mutagenesis
Can be caused by environmental agents that damage
DNA
- UV light
- X-rays and g-rays
- Chemical carcinogens e.g. cigarette smoke
DNA damage can lead to mutations unless it is
removed by DNA repair enzymes Unrepaired damage
can have serious consequences
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16????????????
1000
17Somatic vs. germ line mutations
- Somatic ((??? mutations can lead to cancer
- Germ (???/??????) line mutations can lead to
birth defects (??? ????) - Most mutations cause neither
- Some fall in non-coding DNA
- Others are silent
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(?????-??? ?? ?????????)
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(UV)
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23??? ???? ????? ?????? ???????? ??????????
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- 2. ??, ??? ?????? ?????? ?????? ????, ???? ?????
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24Natural causes of mutations??????? ??????? ?"?
???? ????
- Base tautomerization ??????? ?????????
- UV damage ???? ?????
- Spontaneous deamination - ?????????
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????????? - ?????? ?????????
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31define the following types of mutations
- Transitions
- Transversions
- Multisite mutations including
- Inversions
- Duplications
- Deletions
- Insertions
- Substitutions
32define the following types of mutations
- Point mutations including
- Substitutions
- Insertions
- Deletions
- Duplications
- Inversions
33define the following types of mutations
- Point mutations including
- Substitutions
- Insertions
- Deletions
- Duplications
- Inversions
34define the following types of mutations
- For substitutions you should be able to further
define - Missense mutations
- Nonsense mutations
- Samesense mutations
35Point mutations
- Involve only one or a few nucleotides
- Arise during DNA replication
- Require two errors
- An error during DNA replication
- Failure to correct that error
36Types of point mutations
- Substitutions GATC CATC
- Insertion GATC GGATC
- Deletion GATC GTC
- Duplication GATC GAGATC
- Inversion GATC GTAC
37Types of substitutions
- Missense Results in an amino acid substitution
- Nonsense Results in a stop codon (TAG, TAA,
TGA) - Samesense No effect (silent mutation)
38What is the first defense against mutations?
- 3 to 5 exonuclease activity of the polymerases
39UV Radiation and Pyrimidine Dimers
- UV radiation (200-300 nm) induces the formation
of dimers between adjacent thymine residues - Cytosine-cytosine and thymine-cytosine dimers
occur less frequently - These pyrimidine dimers disrupt the structure of
the double helix, blocking replication until the
lesion is repaired
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41???????? ??????? ?DNA ????? ????? ????????????
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??????? ?????? ??????? ?????? ?? ??????
?????? ??????? ???????? ?DNA ????? ?????????
42Mutations and Cancer
- Mutations that affect nonessential DNA or that
have negligible effects on a genes function are
called silent mutations - Many mutations are detrimental, and a correlation
exists between the accumulation of mutations and
cancer - New chemicals, such as pharmaceuticals, must be
tested for carcinogenic potential - Standard animal tests for carcinogenesis are
lengthy and expensive - The simple Ames test measures the potential of a
given chemical to promote mutations in a
specialized bacterial strain
43The Ames Test for Mutagenesis
- S. typhimurium having a defect in histidine
biosynthesis are plated on a histidine-free
medium - Chemical to be tested is placed on a disk of
filter paper in the center of the culture plate - Revertant bacterial colonies are caused by
mutagens - 80 to 90 of compounds found to be carcinogenic
in animal tests are mutagens in the Ames test
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45Intercalating Agents
- Intercalating agents slip in between stacked base
pairs - Distance between base pairs is doubled by an
intercalating agent - Insertions or deletions of one or more
nucleotides can occur during the replication of
such distorted DNA
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47Chemical Mutagens
- Classes of damage produced by chemical mutagens
- Point mutations one base pair is replaced by
another - Insertions or deletions one or more nucleotide
pairs are inserted in or deleted from DNA - Important types of chemical mutagens
- Alkylating agents ?????????
- Deaminating agents ??????????
- Intercalating agents ???????????
48???????? - Deamination of Cytosine
About 3 of the cytosine residues are methylated
(intentionally).
- Nitrous acid can be formed from nitrite and
nitrate salts - Nitrous acid oxidatively deaminates aromatic
amines - Cytosine is converted to uracil upon treatment
with nitrous acid, causing a GC to AT transition - Cytosine sometimes spontanteously deaminates to
uracil, indicating why DNA contains thymine
rather than uracil
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50???? ???? ??? ???? ?????? ??????? "??????" ?"? BER
About 50 of the time the G is corrected to A
resulting in a mutation
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52Alkylating Agents
?????????
- Alkylating agents such as dimethyl sulfate are
electrophiles - Such agents react most often with the
nucleophilic N7 position of the guanine base - Alkylation at N7 can generate an apurinic site in
DNA - Point mutations occur when guanine is replaced by
another base - DNA methylation can be useful
?????? ?"? BER
53??????? ???????
54Chemical mutagens????? ???????? ???????
????????
- Chemicals that accelerate the deamidation
reaction ?????? ????????? - Base analogues ??????? ???????
- Alkylating agents ?????? ????????
- Intercalation agents - ????????????
55 56???? ????? ????? dsDNA
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62Incorrect bases can swing out facilitating
identification by the DNA repair apparatus
63???? ????? ???????? ????? ?????? ?????? ????
64???? ???? ??? ???? ?????? ??????? "??????" ?"? BER
65Alkylating Agents
?????????
- Alkylating agents such as dimethyl sulfate are
electrophiles - Such agents react most often with the
nucleophilic N7 position of the guanine base - Alkylation at N7 can generate an apurinic site in
DNA - Point mutations occur when guanine is replaced by
another base - DNA methylation can be useful
?????? ?"? BER
66Intercalating Agents
- Intercalating agents slip in between stacked base
pairs - Distance between base pairs is doubled by an
intercalating agent - Insertions or deletions of one or more
nucleotides can occur during the replication of
such distorted DNA
67Overview of DNA repair pathways
- A. Base excision repair
- B. Nucleotide excision repair.
- C. Mismatch repair
- D. Double-strand break repair by
- homologous recombination.
- E. Double-strand break by end joining
68??????? ???????? ????? ????????? ?????? (?? ????)
?"? DNA ????????
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?"? MR
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BER ?? NER
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70- Three general types of DNA repair pathways
- Direct Repair
- Base excision Repair
- Nucleotide excision repair
Direct repair
71DNA Repair
- Many DNA repair mechanisms exist, even in E. coli
- Systems include simple mechanisms to reverse base
modifications and multienzyme systems - O6-methylguanine-DNA methyltransferase transfers
the methyl group from O6-alkylated guanine to one
of its Cys residues - DNA photolyases reverse pyrimidine dimers
- Found in both prokaryotes and eukaryotes, but not
humans - Contain cofactors that use light energy to
mediate electron transfer to the dimer, reversing
the cyclization
72Base excision repair
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74uvrAB recognize the unpair bases
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NER
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77Base-Excision Repair
- DNA glycosylases cleave the glycosidic bonds of
altered nucleotides, leaving an apurinic or an
apyrimidinic (AP) site - Such sites also commonly occur through
spontaneous depurination - Deoxyribose residue is cleaved by an AP
endonuclease - DNA polymerase removes several residues and fills
in the gap - Nick sealed by DNA ligase
78Repair of the daughter strand
Nickase and exonuclease I
G
GATC
Parent
CTAG
New
DNA Pol I and ligase
79Base-excision repair?????
- Deaminated bases are recognized
- Enzymes remove the base
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83Mismatch repair
84Occurs just after replication Improves accuracy
102 - 103 fold Must distinguish the parent from
the daughter strand
Mismatch repair ???? ??? ??? ?????
?????????. ???? ?????? ??? ???? ??? ???? (?"?
???????). ???? ????? ?????? ????? ???? ????
???????. ???? ???? ???????? ?? 100-1000.
Occurs just after replication Improves accuracy
102 - 103 fold Must distinguish the parent from
the daughter strand
85?? ????? ??? ????? ??? ??????? ?-mismatch repair
(MR) ???? ?????? ?-nucleotide excision repair
(NER) ?
- 1. ????? ?????? ??? ???? ????? ???
- 2. ?-MR ???? ???? ?-G1 ???? ??-NER ???? ?-M
?????? ???. - 3. ?-MR ???? ???? ?-M ???? ??-NER ???? ?-G1
?????? ???. - 4. ?-MR ???? ???? ?-G0 ???? ??-NER ???? ?-G1
?????? ???.
86Instability Mutation and DNA repair
- DNA repair
- E-coli mismatch repair
- Human mismatch repair
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89Instability Mutation and DNA repair
- DNA repair
- Human mismatch repair
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92Mismatch repair
- Occurs just after replication
- Improves accuracy 102 - 103 fold
- Must distinguish the parent from the daughter
strand
93What happens when mismatch repair fails in humans?
- Missing enzymes homologous to MutS and MutL
- Patients usually die by age 30
- Disease hereditary nonpolyposis colorectal (???
??) cancer (HPCC) - 1 in 200 people affected
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95Nucleotide Excision Repair (NER)
- NER involves the removal of an oligonucleotide
containing a lesion and replacement of the
resulting gap - Three enzymatic activities are responsible for
this process in E. coli - UvrABC endonuclease
- DNA Pol I
- DNA ligase
- NER mechanisms are similar in humans, but are
much more complex
96Nucleotide excision repair
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97?? ??????? ???? ????? ?? ?????? ?- 1NER
98?? ??????? ???? ????? ?? ?????? ?- 2 NER
993 NER
100(NER) Nucleotid Excision Repair
101Nucleotide-excision repair?????
- Enzymes recognize a kink in the DNA
- Nicking
- Removal of the damaged strand
- DNA polymerization
- Ligation
102Excision repair of thymine dimers (UV-induced)
Repair enzymes remove damaged region
A C G
A T A A C T G C
Gap refilled by DNA polymerase and DNA ligase
Correct sequence restored
103Double strand breaks can give rise to
translocations
Novel genes formed at the fusion junctions can
have deleterious effects
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105Homologous End-Joining recovers information from
the homologous chromosome
Information lost
A
Crossing over
Information restored
106Homologous End-Joining recovers information from
the homologous chromosome
A
Note The sequence of the paternal chromosome is
now identical to the maternal chromosome in the
repaired region -- ie. heterozygosity is lost
107Occurs During Meiosis
108Meiotic recombination results in swapping of
large regions between homologous chromosomes
109Overview of DNA repair pathways
- A. Base excision repair
- B. Nucleotide excision repair.
- C. Mismatch repair
- D. Double-strand break repair by
- homologous recombination.
- E. Double-strand break by end joining
110????? ?????? ?? ????? ????? ????????
111????? ?????? ?? ????? ????? ????????
112???? ?????? ?? ????? RecA
113Post replication recombination repair
114Post replication recombination repair
115Double-strand break repair
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119Post replication recombination repair
120????? ?????? ?? ????? ????? ????????
121SOS repair
122Overview of DNA repair pathways
- A. Base excision repair
- B. Nucleotide excision repair.
- C. Mismatch repair
- D. Double-strand break repair by
- homologous recombination.
- E. Double-strand break by end joining
123Homologues recombination
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