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Lecture 46 – Lecture 47 – Lecture 48 Complex Patterns of Inheritance Ozgur Unal 1
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2 In the pictures below, you see two snapdragon flowers (one red, RR, and one white, rr). When you cross them, the daughter flowers are all pink, Rr. How can you explain this? Which allele is dominant? Which allele is recessive?
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3 In incomplete dominance, the heterozygous phenotype is an intermediate phenotype between the two homozygous phenotypes. When the heterozygous F1 generation snapdragon plants are allowed to self-fertilize, the flowers are red, pink and white in a 1:2:1 ratio.
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4 There is another type of complex inheritance pattern called codominance. In codominance, both alleles are expressed in the heterozygous condition. Example: Sickle cell disease. A person with a sickle cell disease has abnormal red blood cells C-shaped elongated red blood cells If a person is homozygous for the sickle cell trait, all red blood cells have this abnormal shape. If a person is heterozygous for the sickle cell trait, some red blood cells are normal and some red blood cells are C-shaped. This means that the allele for normal blood cells and the allele for sickle cell are both dominant codominant
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5 Example: Checkered chicken Consider the black chickens, BB and white chickens, WW. When these two are allowed to mate, how do you think the daughter chickens look like? Since black and white are codominant, the daughter chickens will have black and white feathers.
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6 So far, you have learned about inheritance involving two forms of allele for a trait (yellow-green seed color etc). Some traits are determined multiple (three or more) alleles. Example: Blood type ABO blood groups have three forms of alleles (AB markers): I A is blood type A I B is blood type B i is blood type O i is recessive to I A and I B. However, I A and I B are codominant. Blood also has Rh factor, inherited from each parent. Rh factors are either positive or negative (two alleles) Rh+ is dominant to Rh-.
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7 Example: Coat color of rabbits Coat color of rabbits is determined by 4 alleles: C, c ch, c h, c Multiple alleles can demonstrate a hierarchy of dominance. Allele C is dominant to c ch, which is dominant to c h, which is dominant to c C > c ch > c h > c C full color c ch chincilla c h himalayan c albino Check out Figure 11.7
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8 What are the differences between the following Labrador retrievers? The fur color of these dogs are determined by the interaction of two sets of alleles (E, e and B, b) The allele E determines whether the fur has a dark pigment The allele B determines how dark the pigment is. e allele masks the effects of the dominant B allele epistasis The interaction in which one allele hides the effect of another allele is called epistasis.
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9 Each cell in your body, except for gametes, contains 46 chromosomes, or 23 pairs of chromosomes. One pair of chromosomes, called sex chromosomes, determines an individual’s gender. There are two types of sex chromosomes: X and Y The other 22 pairs of chromosomes are called autosomes. The offspring’s gender’s determined by the combination of sex chromosomes during fertilization.
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10 Consider the X and Y chromosomes Y is shorter than X X chromosome carries a variety of genes that are necessary for the development of both males and females. Y chromosome mainly has genes that relate to the development of male characteristics. Because females have two X chromosomes, it seems as though females get two doses of X chromosome and males get one dose. To balance the difference, one of the X chromosomes stops working in each of the female’s body cells dosage compensation or X-inactivation Which X chromosome stops working in each body cell is a completely random event.
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11 Example: Calico cat The coat of the calico cat has black and orange colors. These different colors are a result of random inactivation of a particular X chromosome. Orange patches are formed when X chromosome carrying the black coat color is inactivated. Black patches are formed when X chromosome carrying the orange coat color is inactivated.
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12 Barr Bodies: The inactivated X chromosomes can be observed in cells. In 1949, Canadian scientist Murray Barr observed inactivated X chromosomes in female calico cats. The darkly stained, inactivated X chromosomes are called Barr bodies.
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13 Look at the picture below. Can you read the number in the picture? Red-green color blindness is a sex-linked trait. Traits controlled by genes located on the X chromosome are called sex-linked traits (also called X-linked traits) Since males have only one X chromosome, they are affected by recessive X-linked traits more often than females. Females likely would not express a recessive X-linked trait.
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14 Red-green color blindness: The trait for color blindness is a recessive X-linked trait. 8% of males in the US have red-green color blindness. Consider a mother carrier for color blindness and a father who is not color blind. Their daughter will not have color blindness. Their son might be color blind (50% chance)
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15 Hemophilia: Hemophilia, another recessive sex-linked trait, is characterized by delayed clotting of the blood results in death when the blood flow cannot be stopped. More common in males than females. Check out Figure 11.13 for hemophilia disease in the Royal Family.
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16 Name all the eye colors you know. How do your eye color compare to your parents’ and siblings’ eye colors? Many phenotypic traits, such as eye color, arise from interaction of multiple pairs of genes polygenic traits Example: Skin color, height, eye color, fingerprint are polygenic traits.
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17 The environment also has an effect on phenotype. Example: Tendency to develop a heart disease can be inherited, but diet and exercise can reduce the seriousness and the risk. Sunlight, water and temperature are examples of some environmental factors. Sunlight and water: Lack of sunlight affects flowering plants no flowers Many plants lose their leaves in response to water deficiency Temperature: Arctic fox changes fur color with the seasons
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18 Twin studies: Identical twins help scientists study inheritance patterns Identical twins also allow scientists separate genetic contributions from environmental contributions. The percentage of twins who both express a given trait is called a concordance rate. Check out Figure 11.16 for concordance rates for different traits.
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