1 / 18

Mutation

Mutation. دانشگاه علوم پزشكي وخدمات بهداشتي درماني تهران. Dr. Parvin Pasalar Tehran University of Medical Sciences. Mutation. Definition: An un- repaired damages to DNA Causes: It may be spontaneous or induced because of different agents Classifications:

aelan
Télécharger la présentation

Mutation

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Mutation دانشگاه علوم پزشكي وخدمات بهداشتي درماني تهران Dr. Parvin Pasalar Tehran University of Medical Sciences

  2. Mutation • Definition: Anun- repaired damagesto DNA • Causes: It may be spontaneousor induced because of different agents • Classifications: are classified on different basis • Their importance: Genetic Disease& raw material for the development

  3. Different Causes of mutations: Contrary to popular belief… Most DNA damage is caused by endogenousmutagens Estimated DNA damage/day in human cells SSBs ~50,000/day Depurinations ~10,000/day Deaminations ~600/day Oxidations ~2000/day Alkylations ~5000/day DSBs ~50-100/day -

  4. Classifications of Mutations 1- Can be spontaneous or induced 2- May be substitutions or frameshift 3- May occur in structural or regulatory sequences 4- May be small (point) or big 5- May have no or severe effect 6- Somatic or germinal

  5. Different Causes of Mutations • Biological (normal error rate in DNA metabolic processes) • Physical (Radiation) Sunlight • Chemical (Mutagens, Carcinogens) 1- Alkylating agents 2- Base analogues 3- intercalating agents 4- Different chemicals such as: a- Nitrous acid b- Hydroxylamine

  6. Different Type of DNA damages • 1- Double-strand breaks (DSBs) • 2- Single- strand breaks (SSBs) • 3- Base alteration / damage a: Oxidation b: Alkylations c: Hydrolysis depurination deaminations

  7. DNA Damage, Repair, and Consequences Damaging agent Consequences • In hibition of: • Replication • Transcription • Chromosome segregation • Mutation • Chromosome aberration Repair Process

  8. Can we detectMutagen: Ames Assay Bruce Nathan Ames Brith:1928 Ames test: 1970

  9. Repair دانشگاه علوم پزشكي وخدمات بهداشتي درماني تهران Dr. Parvin Pasalar Tehran University of Medical Sciences

  10. 4. Recombinational repair - multiple pathways - double strand breaks and interstrand cross-links Tolerance mechanisms - lesion bypass - recombination DNA Repair Pathways 1. Direct reversals 2. Excision repair a. Base excision repair (BER) b. Nucleotide excision repair (NER) • 3. Mismatch repair • - replication errors

  11. 1-Direct reversal: photoreactivation T T T T Visible light Damage Recognized: Thymine dimers 6-4 photoproduct Gene Products Required: Photolyase Related disease: Photolyase not yet found in placental mammals

  12. 2-Excision Repair Pathways • a. Base Excision Repair • damaged bases are removed as free bases • primarily responsible for removal of oxidative and alkylation damages • most genes in pathway are essential • thought to have an important role in aging • b. Nucleotide Excision Repair • damaged bases are removed as oligonucleotides • primarily responsible for removal of UV-induced damage and bulky adducts • also removes ~ 20% of oxidative damage • deficient in human disorders

  13. 2-Excision Repair Pathways BER NER DNA Ligase DNAP+ Ligase DNAP+ Ligase

  14. Genetics of NER in Humans 1- Xeroderma PigmentosumOccurrence: 1-4/106 population Sensitivity: sunlight Disorder: multiple skin disorders; malignancies of the skin neurological and ocular abnormalities Biochemical defect: early step of NER Genetic: seven genes (A-G), autosomal recessive

  15. Genetics of NER in Humans 2- Cockayne’s Syndrome Occurrence: 1 per/ 106 population Sensitivity: sunlight Disorder: arrested development, mental retardation, dwarfism, deafness, optic atrophy, intracranial calcifications Biochemical defect : NER Genetic: five genes (A, B and XPB, D & G) autosomal recessive

  16. 3- Mismatch Repair in E. coli : Decision between right & wrong (methyl-directed) Before replication both strands of GATC are methylated Shortly afte replication it is hemimethylated After a while it becomes fully methylated again

  17. MMR Mutations inHereditary Nonpolyposis Colon Cancer (HNPCC) • MMR mutations in 70% of families • Population prevalence 1: 2851 (15-74 years) • 18% of colorectal cancers under 45 years • 28% of colorectal cancers under 30 years

  18. Summary

More Related