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Mendel and the Gene Idea
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F 1 produces equal amounts of 4 possible genotypes F 2 reveals even more genotypic possibilities (9:3:3:1) Dihybrid cross is equivalent to two monohybrid crosses (12:4 or 3:1) Illustrates the Law of Independent Assortment
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Many genes do not follow a Mendelian inheritance pattern Incomplete Dominance Co-dominance Multiple alleles Pleiotropy Polygenic Inheritance Lethal Dominance Environmental Influence on Gene Expression 3
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The phenotype of the heterozygous genotype is intermediate between the phenotypes of the homozygous genotypes E.g. snapdragons Heterozygotes differ from homozygotes Predictable 1:2:1 ratio Different than “blending” hypothesis No testcross necessary
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Both alleles are dominant and affect the phenotype in two different but equal ways Andalusian chickens show this pattern of inheritance. If you cross a black (BB) chicken With a white (WW) chicken You get black+white speckled (BW) chicken
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More than two possible alleles controlling one trait Example3 alleles in blood type – OAB 4 possible phenotypes = O, A, B, AB 6 possible genotypes Note: this is also an example of co-dominance
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Genes that have more than two alleles More than two alleles exist in a given population However, any one individual only has two of these alleles Example - Coat color in rabbits (4 alleles) Himalayan RabbitFull Color RabbitAlbino Rabbit Chinchilla Rabbit
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Gene influences multiple characteristics A singe gene influences more than one phenotypic trait. Genes that exert effects on multiple aspects of physiology or anatomy are pleiotropic
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Multiple genes have an additive effect on a single character in the phenotype Example: Skin Color or height Usually is described by a bell-shaped curve with majority clustered in the middle
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T/t x T/t = T/T T/t t/t 1 : 2 : 1 ratio at conception 0 : 2 : 1 ratio at birth
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pH of the soil will change the color of hydrangea flowers from blue to pink
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Temperature will affect color change in fur
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Body temperature affects color in Siamese cats Height is affected by nutrition
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In humans, pedigree analysis is used to determine individual genotypes and to predict the mode of transmission of single gene traits 15
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Huntington disease is a progressive nerve degeneration, usually beginning about middle age, that results in severe physical and mental disability and ultimately in death Every affected person has an affected parent Two unaffected parents will not produce affected children. (aa x aa) Both males and females are affected with equal frequency. Pedigrees show no Carriers.
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Dwarfism Polydactyly and Syndactyly Hypertension Hereditary Edema Chronic Simple Glaucoma – Drainage system for fluid in the eye does not work and pressure builds up, leading to damage of the optic nerve which can result in blindness. Huntington’s Disease – Nervous system degeneration resulting in certain and early death. Onset in middle age. Neurofibromatosis – Benign tumors in skin or deeper Familial Hypercholesterolemia – High blood cholesterol and propensity for heart disease Progeria – Drastic premature aging, rare, die by age 13. Symptoms include limited growth, alopecia, small face and jaw, wrinkled skin, atherosclerosis, and cardiovascular problems but mental development not affected.
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Albinism = absence of pigment in the skin, hair, and iris of the eyes Most affected persons have parents who are “normal” (Aa x Aa) The parents are heterozygous for the recessive allele and are called carriers (Aa) Approximately 1/4 of the children of carriers are affected (aa) Close relatives who reproduce are more likely to have affected children. Both males and females are affected with equal frequency. Pedigrees show both male and female carriers. 19
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Congenital Deafness Diabetes Mellitus Sickle Cell anemia Albinism Phenylketoneuria (PKU) – Inability to break down the amino acid phenylalanine. Requires elimination of this amino acid from the diet or results in serious mental retardation. Galactosemia – enlarged liver, kidney failure, brain and eye damage because can’t digest milk sugar Cystic Fibrosis – affects mucus and sweat glands, thick mucus in lungs and digestive tract that interferes with gas exchange, lethal. Tay Sachs Disease – Nervous system destruction due to lack of enzyme needed to break down lipids necessary for normal brain function. Early onset and common in Ashkenazi Jews; results in blindness, seizures, paralysis, and early death.
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MENDEL AND HEREDITY Why we look the way we look...
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