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Announcements 1. You should be finishing “Monk in the garden” and starting to answer questions for writing assignment. We will discuss this next week. 2. Dr. Brad Swanson is guest lecturing on conservation genetics on Monday. This material will be on Exam 2. 3. “Problem set 2” answers due today at start of class. 4. If you’re in Group A for presentations, I encourage you to discuss your main source/reference with me. Plan ahead! Group A presents in 11 or 12 days. 5. Pay special attention to “Insights and Solutions” - Ch .4, p. 104-106. 6. Study this weekend! Your exam next week is Thursday and Friday. Avoid lines, go early in the day on Thursday. Give yourself enough time to finish the exam. BIO 326- Genetics Fall 2002 Writing assignment on ТThe Monk in the GardenУ by Robin Marantz Henig Choose one of the following th ree topic areas to write a 2-4 page, doublespaced, typed essay. This assignment is worth 75 pts (out o f a possible 1000). You will be graded on: how w ell did you answer the q uestions? (40); do you have good logical flow and organization of your essay? (15); do you have good use of references? (10); and is your s pelli ng and grammar correct? (10) Due date: in lab either 10/1 or 10/2 1) Disc uss several of the reasons that we now acknowledge Mendel as the father of genetics. You should mention some of the practical iss ues that resulted in MendelХsexperiments successfully unlocking the secrets of heredity. You should also discuss some of the reasons his ТgeniusУwas not widely k nown unt il 35 years after he presented his findings on the Тlaws of inher itanceУ. Lastly, present an argument on whether or no t Mendel w as truly a ТgeniusУ. Support your stance with specific examples form the book. 2) W hich of t he three rediscoverers do you most respect and why? Cite examples from the book to explain your answer. What aspects of Тbeing a scientistУ surprised or interested you as you l earned about th e personalities of Mendel and his rediscoverers? Cite specific examples from the book and explain why y ou w ere surprised or interested. 3) H ow c ould DarwinХstheories of evolution and MendelХstheories of inhe ritance have i nfluenced one another? IF they had crossed paths, who might have benefited more from knowing the otherХs work? Explain why. How did theo ries of evolutionary c hange influence each of the thre e rediscoverers? Oral Presentations - BIO 326 Genetics Fall 2002 Group A: Sept. 24, 25 Р in lab; Group B: Oct. 29, 30 Р in lab Assignment: worth 75 pts of total 1000 1) Choose any genetics-related topic and title your presentation 2) Research th e topic using at least one source outside your text and the internet. An example is an article from a respected magazine such as Time or Newsweek, or from a scientific journal such as Scientific American, Ge netics, or Trends in Genetics. You may also use the te xt and internet to supplement your main source(s). 3) Choose 1-2 visual aids to use in your p resentation- overheads or powerpoint slides are acceptable forms to use. 4) Organize your 5-10 minute ta lk suc h tha t you 1) introduce your topic and explain why you chose it; 2) share what you learned; and 3) explain how i t relates to a topic from class. 5) Practice it for a friend; know how long it will go; be prepared. 6) On the day of your talk, turn in a title for your talk wi th the outside source(s) you used. 7) Take questions from your classmates at the end of your talk. Grading: appropriate visual aid (15 pts); introduction of topic (10 pts); explanation of what you l earned (15 pts); relationship to class topics (10 pts); answering questions (10 pts); appropriate source/reference (15 pts). Review of last lecture 1. Incomplete dominance vs. Codominance 2. Multiple alleles of a gene -studied in a population ex. Blood group alleles, A, B, AB, O 3. Lethal alleles - recessive or dominant -can lead to modified Mendelian ratios such as 2:1 genotypic and phenotypic ratios in the F1 4. Modification of the 9:3:3:1 ratio: examining inheritance of two gene pairs that have different modes of inheritance Modified Dihybrid Cross: First Consider Each Trait on its Own Ex. 2 humans heterozygous for albinism and are blood type AB Modified Dihybrid Cross: Next Consider Both Traits Together Outline of Lecture 8 I. Epistasis - genetic interaction affecting expression of one trait II. Novel phenotypes due to gene interaction III. Complementation analysis IV. X-linkage and color blindness V. Is phenotype always completely due to genotype? I. Epistasis • Two or more separate genes (not separate alleles at one genetic locus) interact to control a phenotypic character. • If one gene locus prevents the expression of a second gene, the first locus is epistatic to the second, and the second is hypostatic to the first. Example 1: H/h and AB pathway A antigen A allele HH or Hh Precursor H substance H Substance hh B allele B antigen Epistasis example 2: Coat color in mice Wt coat color is agouti - A (dominant to black); Nonagouti (black) coat color - a Pigmentation expression - B (dominant to albino); No pigmentation (albino) - b If individual is bb, then is albino regardless of allele at a locus due to gene interaction. Agouti Markings • A- hair made with bands of black pigment and yellow pigment. • Aa hair all black. Coat color example of epistasis, cont. AABB (agouti) x aabb (albino) Genotype Phenotype AaBb x AaBb A-BA-bb aaBaabb agouti albino black albino AaBb (all agouti) F2 ratio Final phenotypic ratio 9/16 3/16 3/16 1/16 9/16 4/16 3/16 Due to gene interaction, we see a 9:3:4 F2 ratio. The b locus is epistatic to the a locus. Example of dominant epistasis, a 12:3:1 ratio Inheritance of fruit color in summer squash: two loci together control color and a dominant allele at one locus can mask the expression of the alleles at the second locus. A--- white aaB- yellow aabb green A is dominant to a, and the a locus is epistatic to the b locus. Therefore, if AaBb is crossed to AaBb, the F2 is as follows: A-BA-bb aaBaabb white white yellow green 9/16 3/16 3/16 1/16 12/16 white 3/16 yellow 1/16 green II. Novel phenotypes and F2 ratios due to gene interaction Summer squash fruit shape inheritance: AABB - disc shape x aabb - long shape F1 = AaBb - disc shape F2 = A-BA-bb aaBaabb disc sphere sphere long 9/16 3/16 3/16 1/16 9/16 disc 6/16 sphere 1/16 long Summary of modified F2 ratios - was Mendel just wrong? No, none of these cases has violated the principles of segregation and independent assortment - just added complexity. Practice Problem In a plant, a tall variety was crossed with a dwarf variety. All F1 plants were tall. When two F1 plants were interbred, 9/16 of the F2 were tall and 7/16 were dwarf. Explain the inheritance of height by a) indicating the number of gene pairs involved and b) by designating which genotypes yield tall and which yield dwarf. 1. When studying a single character, a ratio expressed in 16 parts suggests that two gene pairs are “interacting” during the expression of the phenotype. 2. A 9:7 ratio implies a dihybrid condition with epistasis. 3. From any dihybrid cross of double heterozygotes, we see the following genotypic ratio: A-BA-bb aaBaabb 9/16 3/16 3/16 1/16 tall dwarf dwarf dwarf 4. In our problem, we see a 9:7 phenotypic ratio. If the 3:3:1 groups above were lumped together, a 9:7 ratio emerges. Assign tall to any plant with both A-B- and dwarf to any plant that is homozygous recessive for either or both the recessive alleles. III. Complementation Analysis Reveals Whether 2 Mutations are at the Same Locus The mutations do complement each other, so they are in different complementation groups. Mutations do not complement, so in same complememtation group. IV. X Linkage • Affects males and females differently • Example: red-green color blindness • Other examples in humans: – Hemophilia – Duchenne’s muscular distrophy “3” or “8”?? X-linkage means genes on X chromosome • Sex chromosomes are “unlike” in many species; all others are autosomes. • In humans and Drosophila, males contain XY and females contain XX. • Y chromosome contains region of pairing homology with X: pseudoautosomal region. • Y contains few genes; X contains many. Color Blindness Pedigree Males are hemizygous for this gene locus; only females can be carriers. Hemophilia in the European Royal Families • Disorder is lethal or debilitating prior to reproductive maturation. • X-linked recessive: heterozygous females are carriers with 50% chance of passing trait to sons only. • Arose from spontaneous mutation in Queen Victoria? • Hemizygous males were affected in Russian, German, Spanish royal families, trait not passed on in British royal family. V. Is phenotype always due to genotype? Penetrance vs. Expressivity If 70% of the individuals show the mutant phenotype, then the penetrance is 70%. Expressivity reflects the range of expression of the mutant genotype. Variable penetrance or expressivity? Temperature effects on phenotype Temperature can affect coat coloration. Siamese cat fur in the extremities is darker due to cooler temperatures. The enzyme making darker pigment doesn’t work well at the higher temperatures in the rest of the body. Temperature also affects primrose flower color and fur of Himalayan rabbits. Influence of chemicals on phenotype PKU: phenotype is mental retardation due to metabolic disorder; severity is affected by diet and whether phenylalanine is restricted in the diet. Phenocopies: non-hereditary phenotypic modification that mimics a phenotype caused by a known gene mutation. example: deafness can be caused in a developing baby if a mother is infected with rubella during the first 12 weeks of pregnancy; also caused by homozygous, recessive mutation Summary of section V Variation in most of the genetic traits that we have considered so far is determined predominantly by differences in genotype. For many traits, however, the traits are influenced by both genes and the environment. Nature vs. Nurture debates for human behaviors: Ex. Considerations for the weekend/ alcoholism: genes influence how susceptible you are to alcohol abuse but they do not force you to drink alcohol!