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Chapter 14 – Mendel and the Gene Idea
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Mendelian Genetics Character – heritable feature
Trait – variant for a character True-bred – all offspring of same variety Hybridization – crossing of 2 different true-breds P generation – parents F1 (first filial) generation F2 (second filial) generation
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Mendel’s Law of Segregation
Alternative versions of genes (alleles) account for variations in inherited characteristics For each character, an organism inherits 2 alleles, one from each parent If the two alleles differ, then one, the dominant allele, is fully expressed in the organism’s appearance; the other, the recessive allele, has no noticeable effect on the organism’s appearance The alleles for each character segregate (separate) during gamete production (meiosis).
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Genetic Vocabulary Punnett square: predicts the results of a genetic cross between individuals of known genotype Homozygous: pair of identical alleles for a character Heterozygous: two different alleles for a gene Phenotype: an organism’s traits, physical appearance Genotype: an organism’s genetic makeup Testcross: breeding of a recessive homozygote with a dominate phenotype (but unknown genotype)
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Law of Independent Assortment
When tracking the inheritance of 2 or more traits at the same time. Each pair of alleles segregates independently of other pairs of alleles during gamete formation. Genes must be located on different chromosomes.
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Exceptions to Mendel’s Rules
Challenge: a rooster with grey feathers is mated with a hen of the same phenotype. Among their offspring, 15 chicks are grey, 6 are black, and 8 are white. What is the simplest explanation for this pattern? What phenotypes would you expect in the offspring resulting from a cross between a grey rooster and a black hen? Incomplete dominance: heterozygous genotype expresses a phenotype that is between the phenotypes of the 2 parents, Ex: snapdragons Codominance: heterozygous genotype expresses a phenotype that is a combination of both phenotypes, Ex: cattle/horse coat color (roan) and Tay-Sachs disease in humans
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Exceptions cont. Multiple alleles: 3 or more alleles for a given trait, Ex: ABO blood types – has 3 alleles, IA, IB, and i. Challenge: A man with type A blood marries a woman with type B blood. Their child has type O blood. What are the genotypes of these individuals? What other genotypes, and in what frequencies, would you expect in offspring from this marriage?
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Exceptions cont. Pleiotropy: genes with multiple phenotypic effects, Ex: sickle-cell
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Exceptions cont. Epistasis: a gene at one locus affects the phenotypic expression of a gene at a second locus, Ex: mice coat color, Labrador retriever coat color Challenge: A pale yellow Labrador retriever is mated with a black retriever. In their litter of puppies all 4 Labrador colors are observed. What are the genotypes of the parent dogs? Determine the probability of each color of puppy
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Exceptions cont. Polygenic Inheritance: an additive effect of two or more genes on a single phenotypic character, Ex: human skin pigmentation and height
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Human traits Pedigree – shows family history for a trait
Two examples: widow’s peak and earlobes
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Human traits cont. Recessively inherited disorders:
Cystic fibrosis – most common lethal genetic disease in US (mainly European descent), most die before age of 5 Sickle-cell disease – hemoglobin sickle cells aggregate into large clumps causing clots (most common inherited disease in African-Americans) Carriers – heterozygous for a recessive trait, may suffer from some aspects of the disorder and can transmit the disorder to their offspring Dominantly inherited disorders: Acondroplasia – dwarfism Huntington’s disease – degenerative disease of the nervous system, phenotypic affects visible around 40 years of age
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Genetic Testing – fetal testing
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