Unit 3: DNA and Genetics Module 9: Human Genetics

Transcription

1 Unit 3: DNA and Genetics Module 9: Human Genetics NC Essential Standard: 3.2 Understand how the environment, and /or the interaction of alleles, influences the expression of genetic traits Evaluate ethical issues surrounding the use of DNA technology Draw a pedigree that shows a mom and dad that have two girls, one boy. The boy is married. Indicate that all of the males have the trait. Do some diseases run in families? YES! Diseases that are caused by faulty genes are inherited in a family. A genetic disorder that you may have heard of is Sickle-Cell Anemia. The inheritance of these disorders in a family can be displayed in a PEDIGREE. Other genetic disorders are caused by faulty chromosomes and generally result from mistakes in meiosis rather than being passed through a family. A chromosomal disorder you may have heard of is Down s syndrome. I. How can you study human heredity? 1. determines how often a trait appears in a small, randomly selected group. This percentage is then applied to the entire population to predict the number of individuals with that trait. 2. Pedigrees graphically record the over several generations. Typically, the occurrence of the trait is determined based on family/historical documents, interviews, photographs, and medical records. a. Specific are used to represent individuals in a pedigree: Individual With Trait Without Trait Female Male 113

2 b. Connecting lines are used to indicate among individuals within the family. P 1 (parental) F 1 (first filial) F 2 (second filial) Signs a pedigree shows a trait that is Recessive Sex-linked c. Pedigrees demonstrate the (dominant/recessive, sex-linked) of the single trait. i. A dominant trait is likely to be present in ii. A recessive trait may iii. A sex-linked trait is most often seen in d. Pedigrees can be interpreted to determine the presence of (individuals who do not express the trait but may pass the gene on to offspring). Example: The two parents (P 1 generation) must have been carriers (Bb) for a recessive trait. Neither showed the trait, but they had a child with the trait (bb). Check Yourself! 1. In a pedigree, what shape represents a male? 2. What are lines used to indicate, in a pedigree? 3. What do pedigrees tell us about the inheritance of a trait in a family? 114

3 II. What does autosomal mean? List genetic diseases that are Dominant: Codominant: Recessive: How do you get a genetic disease? A. Gene disorders are inherited as a on a chromosome. Most gene disorders are. Thus, in order to express the disorder, the individual must be homozygous recessive. Science hypothesizes that gene disorders arose from that disabled specific proteins, or increase production harmfully. 1. Autosomal genetic diseases occur when the gene defect is on of chromosomes (called the autosomal chromosomes). a. Huntington s disease is inherited as an autosomal gene. Huntington s disease breaks down certain areas of the. In addition to being dominant, Huntington s is also unique because symptoms begin appearing in the person s late forties. b. Sickle-cell anemia is inherited as a autosomal gene. Sickle-cell anemia leads to which lead to poor circulation and pain. Sickle cell is unique because heterozygous individuals are not afflicted by sickle cell AND are able to resist malaria (which is handy in certain areas of the world). Currently, sickle cell is primarily in African populations. c. Cystic fibrosis is inherited as a autosomal gene. Cystic fibrosis leads to in lungs and digestive tract, which may be fatal. Currently, this disease is primarily in Caucasian populations. d. Tay-Sach s is inherited as a autosomal gene. Tay-Sach s leading to premature death (2-4 years of age). Currently, Tay-Sach s is primarily in Jewish and Pennsylvania Dutch populations. 115

4 Watch It! Contrast autosomal with sexlinked using a T-chart or Venn below. Include specific diseases: e. Phenylketonuria (PKU) is inherited as autosomal gene. PKU leads to the when ingested. The phenylalanine builds up in the brain and leads to decreased mental function. PKU is unique because, if detected early, it can be entirely controlled by diet. Individuals can simply not consume products containing phenylalanine (dairy, breads, proteins, etc). However, any damage done before detection is irreversible. In hospitals, children are tested at birth. 2. Sex-linked genetic diseases occur when the gene defect is on the of chromosomes (called the sex chromosomes). Because males inherit only a single X chromosome (they are XY) and the X carries the majority of sex-linked genes, are MORE LIKELY to express sex-linked disorders and cannot be carriers of these traits. a. Hemophilia is inherited as a recessive sex-linked gene. Hemophilia leads to which leads to excessive bruising and bleeding. b. Red-green color blindness in inherited as a recessive sex-linked gene. People with red-green color blindness are colors (both colors often appear a muddy brown). B. Chromosomal disorders are inherited due to (which may contain hundreds of genes!) Thus, an individual with even one chromosomal defect will most likely express the disorder. Science hypothesizes that chromosomal disorders arise from during gamete formation. For example, a sperm cell may receive 22 instead of

5 WORD HELP! non - disjunction is the state of being disconnected List 3 disorders caused by an aneuploidy: chromosomes. This incorrect distribution of chromosomes is called nondisjunction. Nondisjunction may lead to aneuploidy - an in a fertilized zygote. 1. An autosomal chromosome aneuoploidy refers to having. For example, Trisomy 21 (three #21 chromosomes), leads to Down s Syndrome. Characteristics of Down s Syndrome include some level of, heart defects, flat facial features, and an enlarged tongue. 2. A sex chromosome aneuploidy refers to having one extra or one too few sex chromosomes. a. Turner s Syndrome is the result of inheriting a (genotype XO). These individuals are female but lack, are infertile, and have some lack of mental function. b. Klinefelter s Syndrome is the result of inheriting an (genotype XXY). These individuals are male but lack secondary sex characteristics, are, and have some lack of mental function. Check Yourself! 1. What is the difference between a gene disorder and a chromosomal disorder? 2. What is the difference between an autosomal disorder and a sex-linked disorder? 3. Why is hemophilia considered a sex-linked disease? 4. What is an aneuploidy? 117

6 III. What genetic disorder is present in this karyotype? Can we tell if a baby has a genetic disease? A. A genetic counselor can help prospective parents determine the to their offspring and may suggest further testing procedures. Counselors may also interpret diagnostic procedures done by the doctor for parents. 1. Sonograms / ultrasounds use sound waves to of the developing fetus. This may be used to detect physical abnormalities (such as cleft palate). 2. Blood tests of the pregnant mother may to assess the risk level of certain genetic disorders 3. Amniocentesis removes containing fetal cells. The cells are then cultured until mitosis occurs and the chromosomes are visible. A karyotype ( ) is made using the visible chromosomes. The karyotype allows doctors to and the sex of the child but does NOT detect gene abnormalities because the gene sequence is molecular, and not visible. How do you know? What is the sex of this person? How do you know? 4. Chorionic villi sampling (CVS) removes actual tissue from the (which is composed on embryonic cells) in order to. This may be done earlier in the pregnancy, but is far more invasive and thus riskier. 118

7 B. The Human Genome Project has allowed science to develop certain. A genetic marker detects the presence of certain gene variations on the chromosomes. These genes may either be a direct cause of a disorder or may simply indicate a for a trait. Doctors or genetic counselors may use genetic markers to screen parents and determine if the parents may be carriers for genetic disorders. Check Yourself! 1. Name 4 pre-natal tests that may detect genetic disorders. 2. What is a karyotype? 3. Why aren t individual genes visible on a karyotype? IV. Can you prevent and/or treat genetic disorders? A. Currently, there is no cure for genetic disorders because the disorder. However, the of genetic disorders can be treated and experimental trials for replacing defective genes are underway. Gene therapies are being developed using information from the. These therapies seek to use engineered cell invaders (such as a virus) in order to actually in target cells with a functioning gene. 119

8 What aspect of PKU is Genetic (Nature)? Environmental (Nurture)? B. Environmental factors may play a large role in the. Environmental factors that interact with genes can be controlled to help prevent the eventual expression of known genetic predispositions. 1. Appropriate can stop the progression of PKU. Diet may also limit the risk for genetic predispositions such as heart disease, alcoholism, and certain cancers. 2. Environmental such as UV radiation and tobacco products can directly change our genes. Harmful behaviors (such as smoking) and positive behaviors (such as using sun screen) increase or reduce the likelihood of genetic mutations from these toxins. The mutations may lead to cancers i f protective genes are disrupted. Check Yourself! 1. What is gene therapy? 2. Identify two environmental toxins that may affect genes. 120

9 Genetic Diseases caused by inheritance of a mistake in affecting an entire type based on chromosome which may be Autosomal Autosomal examples include examples include examples include examples include Sickle-cell anemia Word Bank: Chromosome Defective gene Down s syndrome Location Meiosis PKU Sex Chromosome Sex-linked Turner s (XO) 121

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11 Unit 3 / Module 9 Problem-Solving Set 1. The pedigree below shows the inheritance of cystic fibrosis in a family. A B C D a. How many generations are represented in the pedigree? b. What is the pattern of inheritance for cystic fibrosis? c. What is the genotype for individuals A and B? d. Could individual C be a carrier? e. What is the genotype for individual D? 2. The pedigree below shows the inheritance of Huntington s disease. A B C a. How many males are in the pedigree? How many females? b. What is the pattern of inheritance for Huntington s disease? c. What is the genotype for individual A? d. What are the possible genotypes for individual B? or e. What is the genotype for individual C? 123

12 3. The pedigree below shows the inheritance of hemophilia. A B C D a. How many children do the 1 st generation parents have? b. What is the pattern of inheritance for hemophilia? c. What is the genotype for individual A? d. What is the genotype for individual B? e. What is the genotype for individual C? f. What is the genotype of individual D? 4. You are the head geneticist at Bulldog Memorial Hospital and have been presented with several cases to diagnose. Read each of the following patient descriptions, then indicate which genetic disorder the patient is most likely suffering from. Age: 11 months Racial background: Jewish Development appeared to be progressing normally until the last month. The infant exhibits jerky movements, and seems to be losing the ability to smile and lift his head. Age: 42 Racial background: Caucasian Patient has recently begun to experience slurred speech. Body movements are becoming uncontrolable. The patient s father experienced similar symptoms before his death at age 45. Age: 22 Racial background: African-American The patient frequently experiences excruciating pain, especially in the extremities. This is more pronounced after exercise or periods of stress. A recent blood test showed abnormally shaped red blood cells. Age: 7 Racial background: Caucasian Patient has frequent respiratory infections and often coughs up excessive amounts of mucous. She also has difficulty digesting certain types of foods. 124

13 Age: 18 months Racial background: Asian Infant development appears to be progressing more slowly than normal. The patient s eyes are sloped and the tongue is quite large. A karyotype revealed an extra chromosome #21. Age: 5 months Racial background: Caucasian Infant is unresponsive and appears to be developmentally delayed. The mother denied a blood test at birth and has been feeding the child a milkbased formula. Age: 18 Racial background: Caucasian Patient has underdeveloped secondary sex characteristics and also exhibits slight mental retardation. A karyotype revealed that she lacks one sex chromosome. Age: 19 Racial background: Caucasian Patient lacks muscular development and exhibits some degree of female secondary sex characteristics. He is tall and lanky, and is slightly developmentally delayed. Age: 6 Racial background: African American Patient bruises easily and often bleeds profusely from small wounds. Other male members of his family have also experienced these problems. Age: 4 Racial background: Hispanic Patient s mother is concerned that his is unable to learn his colors in kindergarten. He is unable to perform simple tasks such as matching his socks when dressing. 5. Use the karyotypes below to diagnose the chromosomal disorder: Diagnosis: (circle the abnormality on the karyotype) Male or Female? 125

14 Diagnosis: (circle the abnormality on the karyotype) Male or Female? Diagnosis: (circle the abnormality on the karyotype) Male or Female? 5. Explain why gene disorders such as sickle-cell anemia and PKU can not be diagnosed with a karyotype. 6. In the near future, it may be possible for physicians to test for genetic predisposition to problems such as alcoholism or breast cancer. Identify one pro and one con to this technology. Pro: Con: 7. The diagram shows how a virus may be used to insert a normal gene into a cell during gene therapy. Put the steps in the correct sequence: Virus infects human cell Normal gene is inserted into viral DNA Virus delivers its DNA to human cell Image credits: