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What does pedigree mean? Pedigree: a diagram that traces one trait through several generations of a family What are they used for? • Pedigree charts show a record of the family of an individual • They can be used to study the transmission of a hereditary condition • They are particularly useful when there are large families and a good family record over several generations. © 2007 Paul Billiet ODWS Studying human genetics • Pedigree charts offer an ethical way of studying human genetics • Today genetic engineering has new tools to offer doctors studying genetic diseases • A genetic counsellor will still use pedigree charts to help determine the distribution of a disease in an affected family © 2007 Paul Billiet ODWS = female = male Example #1 3 How many girls? ___ 2 How many boys? ___ mom daughter #1 dad daughter #2 son mom dad oldest daughter #1 youngest daughter #2 son A horizontal line connecting two shapes represents a cross/marriage. mom dad Example #2 How many crosses/marriages? 2 A C B D E F G A vertical line extending down from a marriage/cross represents that the couple has children. mom dad A C B D questions… E F G Example #3 A C How many couples have children? B D H H G E F M J N K L O ? P Q R S T 4 How do you show twins? A C B D E F How do you show traits? Shading ( shaded = recessive ) RR Rr rr mutation **A pedigree chart follows one trait. Rr mom RR dad R = tongue roller r = non-roller Rr son Rr daughter RR daughter R R R RR RR r Rr Rr A C B D G E F M Practice questions… J N P HH K L O Q R S T What is wrong with this pedigree chart? This offspring cannot receive 2 recessive genes. This offspring cannot receive 2 dominant genes. This offspring cannot receive 2 recessive genes. What are possible genotypes for individual W? W R r R RR Rr r Rr rr W could be RR (no shading) or Rr (half-shaded) or rr (all shaded). Pedigree charts help to trace genetic diseases. Most genetic diseases are a recessive gene. If you have 1 recessive, you are a carrier, but you are not sick. Aa If you have 2 recessive genes, you are sick with the disease. (you are “affected”) aa Organising the pedigree chart – Generations are identified by Roman numerals I II III IV © 2007 Paul Billiet ODWS Organizing the pedigree chart • Individuals in each generation are identified by Arabic numerals numbered from the left • Therefore the affected individuals are II3, IV2 and IV3 I II III IV © 2007 Paul Billiet ODWS 4 3 Granddaughter, carrier, 3rd generation, older sibling Grandson, carrier, 3rd generation, middle sibling rr Rr 1 7 A person that carries one copy of the disease gene, but it is masked by the dominant trait. (hybrid) 2 U U is further left. This makes U older than V Genetic Pedigree Answers 4 1. How many children did the first generation have? 2. How many girls did the first generation have? 3. Describe individual Y. A female carrier/hybrid 4. Describe individual Z. A male carrier/hybrid 5. How many children and grandchildren have the disease? 6. What is the genotype of X? Use the letter R/r. 7. What is the genotype of Y? Use the letter R/r. 8. How many children and grandchildren are carriers for the disease? 9. 10. 11. 3 1 rr Rr 7 Shows the dominant trait, but can pass the What is a carrier? recessive gene on to offspring. How many kids did W and his wife have? 2 U Who is older, U or V? It comes first left to right How do you know? Goals of Pedigree Analysis • 1. Determine the mode of inheritance: dominant, recessive, partial dominance, sexlinked, autosomal, mitochondrial, maternal effect. • 2. Determine the probability of an affected offspring for a given cross. Sex-Linked Traits • What determines if a baby is a male or female? Recall that you have 23 pairs of chromosomes—and one of those pairs is the sex chromosomes . Everyone has two sex chromosomes. Your sex chromosomes can be X or Y. Females have two X chromosomes (XX), while males have one X chromosome and one Y chromosome (XY). • If a baby inherits an X chromosome from the father and an X chromosome from the mother, what will be the child’s sex? • The baby will have two X chromosomes, so it will be female. If the father’s sperm carries the Y chromosome, the child will be male. Notice that a mother can only pass on an X chromosome, so the sex of the baby is determined by the father. The father has a 50 percent chance of passing on the Y or X chromosome, so there is a 50 percent chance that a child will be male, and there is a 50 percent chance a child will be female. Y-Linked Inheritance • We will now look at how various kinds of traits are inherited from a pedigree point of view. • Traits on the Y chromosome are only found in males, never in females. • The father’s traits are passed to all sons. • Dominance is irrelevant: there is only 1 copy of each Y-linked gene (hemizygous). Sex-Linked Trait/Y-Linked One example of a sex-linked trait is red-green colorblindness. People with this type of colorblindness cannot tell the difference between red and green. They often see these colors as shades of brown ( Figure below ). Boys are much more likely to be colorblind than girls ( Table ). This is because colorblindness is a sex-linked, recessive trait. Interpreting a Pedigree Chart 1. Determine if the pedigree chart shows an autosomal or X-linked disease. – If most of the males in the pedigree are affected the disorder is X-linked – If it is a 50/50 ratio between men and women the disorder is autosomal. Example of Pedigree Charts Is it Autosomal or X-linked? Answer Autosomal Interpreting a Pedigree Chart 2. Determine whether the disorder is dominant or recessive. – If the disorder is dominant, one of the parents must have the disorder. – If the disorder is recessive, neither parent has to have the disorder because they can be heterozygous. Example of Pedigree Charts Dominant or Recessive? Answer Dominant Example of Pedigree Charts Dominant or Recessive? Answer Recessive Summary Pedigrees are family trees that explain your genetic history. Pedigrees are used to find out the probability of a child having a disorder in a particular family. To begin to interpret a pedigree, determine if the disease or condition is autosomal or X-linked and dominant or recessive. Cystic fibrosis (CF) also known as mucoviscidosis, is a genetic disorder that affects mostly the lungs but also the pancreas, liver, kidneys and intestines. Long-term issues include difficulty breathing and coughing up sputum as a result of frequent lung infections. Other symptoms include sinus infections, poor growth, clubbing of the fingers and toes, and infertility in males among others. Different people may have different degrees of symptoms. CF is an autosomal recessive disorder. Pedigree Chart -Cystic Fibrosis