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Chapter 17 Altering the genetic message: Mutation Cancer.

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Chapter 17 Altering the genetic message: Mutation Cancer.
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Page 1: Chapter 17 Altering the genetic message: Mutation Cancer.

Chapter 17

Altering the genetic message:

Mutation

Cancer.

Page 2: Chapter 17 Altering the genetic message: Mutation Cancer.

MUTATIONS

= change in the genetic message

= change in the nucleotide sequence of a gene

= DNA Damage + DNA Repair.

1. Types of mutations

2. Causes of DNA damage

3. DNA (damage) repair

Page 3: Chapter 17 Altering the genetic message: Mutation Cancer.

Types of mutations.

A. Gene mutationsa. point mutations

or base-pair substitutionb. frame-shift mutations

B. Chromosomal mutations(duplication, inversion, deletion, translocation)

Page 4: Chapter 17 Altering the genetic message: Mutation Cancer.
Page 5: Chapter 17 Altering the genetic message: Mutation Cancer.

Causes of DNA damage.

1. Spontaneous (tautomeric shift, deamination, depurination, looping-out)2. Oxidation3. Chemical - base-pair analogs - base-modifying agents - intercalating agents - agents that cause ‘bulky’ lesions4. Physical: - UV light

- X-ray

Page 6: Chapter 17 Altering the genetic message: Mutation Cancer.

Causes of DNA damage.

1. Spontaneous - tautomeric shift

- deamination- depurination- strand slippage/looping-out

Page 7: Chapter 17 Altering the genetic message: Mutation Cancer.

Tautomeric shift of bases

Common Form Uncommon Form

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Tautomeric shift leads to altered base pairing.

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Depurination of DNA

Apurinic sites

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De-amination of cytosine or methyl-cytosine.

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5’TACGGAC 3’3’ATGCCTGACTTTGC 5’

5’TACGGACTG 3’3’ATGCCTGACTTTGC 5’

T

5’TACGGACTGAAACG 3’3’ATGCCTGACTTTGC 5’

T

Strand slippage during DNA replication

Newly synthesized DNATemplate DNA

Newly synthesized DNA loops out, …

… resulting in the addition of one nucleotide in the new strand.

Page 15: Chapter 17 Altering the genetic message: Mutation Cancer.

5’TACGGAC 3’3’ATGCCTGACTTTGC 5’

5’TACGGACTG 3’3’ATGCCTGCTTTGC 5’

A

5’TACGGACGAAACG 3’3’ATGCCTGCTTTGC 5’

A

Strand slippage during DNA replication

Newly synthesized DNATemplate DNA

Template DNA loops out, …

… resulting in the omission of one nucleotide in the new strand.

Page 16: Chapter 17 Altering the genetic message: Mutation Cancer.
Page 17: Chapter 17 Altering the genetic message: Mutation Cancer.

Causes of DNA Damage 2. Oxidative damage

(Respiration, Mixed function oxidases, Inflammation)

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Causes of DNA damage. 3. Physical

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UV-Light(254 – 260 nm)

Pyrimidine dimers

Gross distortionDNA molecule

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Malignant Melanoma

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Causes of DNA damage. 3. Physical

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Causes of DNA damage.

4. Chemical - base-pair analogs - base-modifying agents

- alkylating agents- base deaminating

- intercalating agents - agents that cause ‘bulky’ additions

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Causes of DNA damage

4. Chemical:

Base Analogs

Miss-pairing

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Alkylating agents add alkyl groups Cause altered base pairing

E.g., Ethyl-methane-sulfonate (mustard gas),Nitroso-guanidine.

Page 29: Chapter 17 Altering the genetic message: Mutation Cancer.

Base deamination

E.g., nitrous acid, bisulfite

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ActinomycinEthidium BromideAcriding OrangeTetracyclineProflavine

Intercalating agents

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Bulky additions grossly distort the DNA

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Aflatoxins

… ‘bulky’ additions, gross distortions of

the DNA

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Benzo ( )a pyrene

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Cellular Responses to DNA damage

Error-free DNA repair Apoptosis

Error-prone DNA repair

Mutation

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DNA Repair:

1. Direct correction of DNA repair

a. Proofreading of DNA polymeraseb. Repair of alkylating damage

2. Repair involving excission of base pairs

a. General excission repair system (UvABC)b. Repair by glycosylases and

AP endonucleasesc. Mismatch-repair systemd. SOS-repair system

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Proofreading Capacity of DNA Polymerase

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Repair by Alkyl-transferases

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General Excision repair system

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Xeroderma pigmentosa:Deficiency of the general excision repair system.

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Glycosylase/AP endonuclease

Repair system

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Repair by DNA glycosylaseand AP endonucleases.

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Mismatch Repair System

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Hereditary Non-Polyposus Colon-rectal Cancer (HNPCC)

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Error-prone repair by end-joining.

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Chapter 17

Altering the genetic message:

Cancer.

Page 52: Chapter 17 Altering the genetic message: Mutation Cancer.

Independent of growth signals

Insensitive to growth inhibitors

Changed energy metabolism

Avoid apoptosis

Limitless replicative potential

Sustained angiogenesis

Tissue invasion metastasis

Cancer

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Cancer cells loose contact inhibition, grow on top of each other, and become

rounded.

Normal cells

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Normal Cancer

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Normal(contact inhibition)

Cancer

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Rous sarcoma virus

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Nobel Prize 1989

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Chicken Rous Sarcoma Virus (RSV) carried an oncogene called v-src and this gene was an intronless version of a normal chicken gene called c-src.

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Proto-oncogene(s)

Oncogene(s)

Activetumor suppressor

gene(s)

Inactivetumor suppressor

gene(s)

CANCER

MUTATIONS

Gain-of-function

Loss-of-functionDominant phenotype

Recessive phenotype

DNA Damage+

DNA Repair

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+

Rb EF2

Cdk2-cyclin E

P

DNA

mRNA

DNA polymerase

S-phase

Retinoblastoma.

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A multi-hit process of mutations accumulating in proto-oncogenes and tumor suppressor genes.

CANCER:

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Familial Adenomatous Polyposis Coli

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Colonoscopy Results

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JB Weitzmann and Nosh YanivNature 1999, 400 p401

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What causes cancer?

1. Environmental carcinogens

- chemical (e.g., cigarette smoke)- physical (e.g., UV radiation)

2. Host carcinogens (e.g., inflammation)

3. Viruses:

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Page 85: Chapter 17 Altering the genetic message: Mutation Cancer.

TUMOR VIRUSES

Papiloma virus

Hepatitis B virus

Human Herpes virus 8 (Kaposi)

Human Herpes virus 4 (Epstein Bar)

Human T lymphotropic virus

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This woman has hepatitis B and is suffering from liver cancer. She was a Cambodian refugee and died 4 months after she arrived in a refugee camp (average life expectancy after diagnosis of liver cancer is 6 months)

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Kaposi syndrome: Human Herpes Virus 8)

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Cutaneous B cell lymphoma

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HTLV Leukemia

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The End.


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