1. Phenylketonuria (PKU) screening

2. Pre-activity assessment questions Note: The first two slides are intended for first-time clicker users to become accustomed to the devices.

3. Where do you live? 1.Baltimore area 2.Washington area 3.Salisbury 4.Other than Salisbury on the Eastern Shore of MD 5.Delaware 6.Somewhere else

4. Have you studied genetics in your school classroom? 1.Yes, a lot. 2.Yes, a little bit. 3.No, not very much. 4.What do you mean by genetics?!?!

5. When a trait is inherited, what actually passes from one generation to the next? 1. Protein 2.DNA 3.RNA 4.Amino acids

6. Which words relate to DNA? 1. Deoxyribonucleic acid 2.Gene 3.Chromosome 4.All of the above.

7. A trait is recessive if 1.the DNA coding for it must be inherited from both parents. 2.the DNA coding for it only needs to be inherited from one parent. 3.no copies of the DNA are inherited from the parents. 4.both parents had the trait.

8. If both parents have a recessive disease, what is the chance that their child will have the same disease? 1.0% 2.25% 3.75% 4.100% 5.Not enough information to answer the question.

9. If neither parent has a recessive disease, what is the chance that their child will inherit a recessive disease? 1.0% 2.25% 3.75% 4.100% 5.Not enough information given.

10. How might you tell if someone has a genetic disease? 1. Test his/her DNA. 2.Test his/her blood. 3.Look for disease symptoms. 4.All of the above.

11. A genetic disease that all newborn babies get tested for is 1. HIV 2.Phenylketonuria 3.Cancer 4.Diabetes

12. All people with PKU are hyperactive and have seizures and rashes. 1. True 2.False

13. People with PKU need to avoid a high protein diet because 1. their DNA binds to it and makes them sick. 2.high protein diets cause heart disease. 3.they have too much phenylalanine in their blood. 4.None of the above.

14. Phenylalanine is a(n) 1. gene 2.protein 3.amino acid 4.disease

15. Simulated Guthrie screen for PKU (Phenylketonuria) Newborn screening for genetic disease

16. Newborn genetic testing Chemical analysis of blood samples Detects lack or excess of important metabolites and hormones Detects red blood cell abnormalities Ideal if fast and inexpensive Ideal to identify and treat diseases as soon as possible Important knowledge for future generations Specific tests vary somewhat from state to state

17. Phenylketonuria (PKU) inheritance Inherited, recessive disease About 1 in 15,000 babies born in the United States inherit PKU. People with PKU (phenylketonurics) can’t break down phenylalanine, a common amino acid All newborns in United States are screened for PKU Neither parent has the disease, but children can inherit it.

18. Phenylketonuria (PKU) Excess phenylalanine, a common amino acid Phenylalanine accumulates, causing rashes, seizures, hyperactivity, and mental retardation, if untreated. No cure. Disease is managed by avoiding foods high in proteins containing phenylalanine. Phenylalanine (Phe)

19. Newborns are screened for PKU All US babies are screened for PKU by heel-prick test. Blood tested for excess phenylalanine. Blood placed on agar plate with bacteria that need phenylalanine to grow. Healthy babies’ blood doesn’t have extra phenylalanine, so bacteria can’t grow Babies with PKU have extra phenylalanine, so bacteria grow

20. Guthrie test for PKU Bacterial plate with newborn blood samples Negative controls: no bacterial growth Positive blood test results: bacterial halo = PKU Negative blood test results: no bacterial growth = healthy babies Positive controls : increasing phenylalanine concentrations give bacterial halos http:// www.childrenshospital.org/cfapps/research/data_admin/Site2940/mainpageS2940P4sublevel15.html

21. Simulated Guthrie screen for PKU Place filter with “newborn blood sample” onto agar plate. Wait 10- 15 minutes. Include positive and negative control samples. – What is used for these controls? Look for agar plate color to change to indicate positive results. Remove filters if necessary. “Blood” samples Positive control Negative control + -

22. Amino acids make proteins Phenylalanine (Phe) is an amino acid found in almost all proteins. 20 amino acids make up all the proteins found in living things. Proteins are chains of linked amino acids that give cells shape or act like machines to do work in cells.

23. Proteins cause most traits in living things Proteins are linked amino acids that give cells shape or act like machines to do work in a cell. Protein sequences are determined by DNA. Keratin protein makes hair Enzyme makes purple pigment GFP makes green fluorescent protein Animal muscles are made of protein.

24. PKU is caused by DNA mutations People with PKU have inherited mutations in the gene coding for a protein that regulates phenylalanine levels. Phenylketonurics have too much phenylalanine in their blood. Excess phenylalanine causes disease symptoms, like mental retardation. Keeping phenylalanine blood levels low allows healthy life.

25. PKU Diet: low protein = low phenylalanine Lofenalac special infant formula, low in phenylalanine Phenylalanine-free nutrient mixes for adults. Little to no milk, cheese, eggs, meat, fish, beans, nuts, or other high protein foods. Fruits and vegetables are the most safe foods. Certain “diet” or “light” foods must be avoided completely.

26. Sickenly sweet Aspartame Aspartame = artificial sweetener made from amino acids phenylalanine and aspartic acid Found in “diet”, “light”, and “sugar-free” foods Highly toxic to people with PKU

27. Do the blood samples you are testing come from babies with PKU?

28. Post-activity assessment questions

29. When a trait is inherited, what actually passes from one generation to the next? 1.Protein 2.DNA 3.RNA 4.Amino acids

30. Which words relate to DNA? 1.Deoxyribonucleic acid 2.Gene 3.Chromosome 4.All of the above.

31. A trait is recessive if 1.the DNA coding for it must be inherited from each parent. 2.the DNA coding for it only needs to be inherited from one parent. 3.no copies of the DNA are inherited from the parents. 4.both parents had the trait.

32. If both parents have a recessive disease, what is the chance that their child will have the same disease? 1.0% 2.25% 3.75% 4.100% 5.Not enough information given.

33. If neither parent has a recessive disease, what is the chance that their child will inherit a recessive disease? 1.0% 2.25% 3.75% 4.100% 5.Not enough information given.

34. How might you tell if someone has a genetic disease? 1.Test his/her DNA. 2.Test his/her blood. 3.Look for disease symptoms. 4.All of the above.

35. A genetic disease that all newborn babies get tested for is 1. HIV 2.Phenylketonuria 3.Cancer 4.Diabetes

36. All people with PKU are hyperactive and have seizures and rashes. 1.True 2.False

37. People with PKU need to avoid a high protein diet because 1.their DNA binds to it and makes them sick. 2.they have too much phenylalanine in their blood. 3.high protein diets cause heart disease. 4.All of the above.

38. Phenylalanine is a(n) 1.gene 2.protein 3.amino acid 4.disease

39. 1.Write down one interesting thing that you learned in this session. 2.Write down one question that you have or something that confused you in this session.

40. Additional slides

41. More multiple choice ideas What is the difference between phenylalanine and PKU ? Phe is a building block for proteins, while PKU is a disease (and variations) What is the relationship between a protein and an amino acid? Amino acids are the building blocks for proteins (and variations).

42. Proteins are coded by DNA DNA sequence determines amino acid sequence in proteins. Amino acid sequence determines protein structure and function. Changes, or mutations, in DNA cause changes in protein’s amino acid sequence. Changes in protein structure cause changes in protein function. Changes in protein function cause altered traits, sometimes disease. trait

43. Proteins cause most traits in living things Proteins are linked amino acids that give cells shape or act like machines to do work in a cell. Proteins are encoded by DNA. Keratin makes hair Enzyme makes purple pigment Phenylalanine hydroxylase enzyme breaks down phenylalanine GFP makes green fluorescent protein

44. PKU is caused by DNA mutations People who inherit PKU have inherited mutations in the gene coding for a digestive protein (enzyme). Phenylalanine hydroxylase enzyme breaks down phenylalanine. Phenylalanine hydroxylase enzyme breaks down phenylalanine Phenylketonurics don’t have working phenylalanine hydroxylase, so they can’t break down phenylalanine. Phenylalanine accumulation causes disease symptoms, like mental retardation.