1. Human Genetic Mutations

2. 2 Main Types of Mutations 1.) Chromosomal Mutations 2.) Gene Mutations

3. What are chromosomes? Humans have 23 pairs of chromosomes, with one chromosome from each parent. The chromosomes are coiled up DNA. Under normal conditions all of the chromosomes are inherited in tact. This is a normal karyotype of human chromosomes. A karyotype is a picture of chromosomes lined up to look at and compare.

4. Chromosomal Mutations Any change in the structure or number of chromosomes Large scale: Affect many genes

5. 5 Types 1.Deletion 2.Duplication 3.Inversion 4.Translocation 5.NonDisjunction

6. Chromosomal Deletion One or more genes are removed Causes: Wolf-Hirschhorn syndrome (severe mental retardation) cri du chat syndrome (mewing sounds, mental retardation)

7. Chromosomal Duplication A segment of genes is copied twice and added to the chromosome Causes: Charcot–Marie–Tooth disease (high arched foot, claw feet, confined to a wheelchair)

8. Chromosomal Inversion a segment of genes flip end-to-end on the chromosome Causes: Four-Ring Syndrome (cleft pallate, club feet, testes don’t descend)

9. Chromosomal Translocation Material is swapped with another chromosome Causes: Burkitt’s Lymphoma (cancer of the lymph nodes, in children)

10. Nondisjunction Chromosomes FAIL TO SEPARATE during meiosis Meiosis I Nondisjunction Meiosis II Nondisjunction

11. Nondisjunction Produces gametes (and therefore a baby) with one missing chromosome or one extra chromosome

12. Nondisjunction (in Meiosis II)

13. Fertilization

14. Nondisjunction Every cell in that baby’s body will have __ copies of this chromosome instead of___. This condition is called ____________. Trisomy 21 = Individual has _____ copies of chromosome # ________

15. Nondisjunction Every cell in that baby’s body will have 3 copies of this chromosome instead of 2. This condition is called __________. Trisomy 21 = Individual has _____ copies of chromosome # ________

16. Nondisjunction Every cell in that baby’s body will have 3 copies of this chromosome instead of 2. This condition is called TRISOMY Trisomy 21 = Individual has __ copies of chromosome # ____.

17. Nondisjunction Every cell in that baby’s body will have 3 copies of this chromosome instead of 2. This condition is called TRISOMY Trisomy 21 = Individual has 3 copies of chromosome # 21.

18. Chromosomal Mutations Most chromosomal mutations are lethal If the fetus survives: Tend to cause wide-spread abnormalities Example: Down Syndrome

19. Down Syndrome Cause: Nondisjunction of chromosome 2 1 Three copies of chromosome 21 = “TRISOMY 21”

20. Trisomy 21 - Down Syndrome

21. Onto gene mutations!

22. Gene Mutations Small scale: one gene is affected Any change to the DNA sequence of a gene: Nucleotides/Bases may be added, missing, or changed

23. Gene Mutations: 2 Types Point Mutation Frameshift Mutation

24. Types of Point Mutations One base (A, T, C, or G) is substituted for another Causes: Sickle-cell anemia 3 Possible Consequences: –nonsense mutations: code for a stop, which can translate the protein –missense mutations: code for a different amino acid –silent mutations: code for the same amino acid

25. Frameshift Mutation One or more bases (A, T, C, or G) are added or deleted Causes: Cystic Fibrosis Caused by: –Insertion: adding a base –Deletion: removing a base

26. Causes of Mutations spontaneous occur during DNA replication Caused by MUTAGENS physical, ex: radiation from UV rays, X-rays or extreme heat or chemical (molecules that misplace base pairs or disrupt the helical shape of DNA).

27. Gene Mutations KEY IDEA: A mutated gene will make a mutated protein Mutant proteins are trouble! –They do not go where they are supposed to go –They do not do what they are supposed to do

28. Example: Sickle Cell Anemia Normal Red Blood Cell Red blood cells shaped like a disc Hemoglobin (protien) carries oxygen to all parts of the body Sickle Red Blood Cell Red blood cells form an abnormal crescent shape Hemoglobin (protein) is abnormally shaped don't move easily through your blood vessels form clumps and get stuck in the blood vessels

30. Example: Cystic Fibrosis (CF) What is it? –Autosomal, recessive disorder Symptoms –Thick mucus in the lungs and digestive track –Constant lung infections and impaired digestion

31. Cystic Fibrosis (CF) Who gets it? –Anyone –Most common in Caucasians Prevalence –1 in ~3,000 Americans has CF –1 in 23 white Americans carries the mutant allele!

32. Cause of Cystic Fibrosis (CF) The “CFTR” gene is mutated –3 base pairs are deleted Mutant protein is missing an amino acid and cannot fold correctly vs

33. Normal CFTR protein: Ion channel in cell membrane

34. KEY POINT #2 Mutation of a gene = Mutant protein Dysfunctional proteins cause the symptoms of the disorder