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Published byDorothy Osborne Modified over 8 years ago
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Chapter 14
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Mendel and Heredity Gregor Mendel – Austrian Munk Worked with heredity in pea plants Wanted to determine how characters and traits were passed from generation to generation Advantages of pea plants: Short generation Large offspring production “either or” traits Self pollinating True breeding
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Mendel’s Cross Fertilization Experiments Crossed 2 distinct versions Created a hybrid True breeding plants were P-generation Offspring were the F 1 If F 1 self pollinated the result was the F 2
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Monohybrid Cross Four principles revealed: Alternate versions of genes account for variations - alleles For each character, organisms inherit 2 copies, one from each parent Alleles may be dominant or recessive Law of segregation
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Punnett Square Used as a predictive tool to show potential offspring Alleles are combined to show possible genetic outcomes Homozygous dominant Heterozygous Homozygous recessive
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Test Cross Used by current geneticists to determine genetype Use of a homozygous recessive crossed with the unknown P? x pp If all purple – PP If half purple, half white - Pp
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Law of Independent Assortment Do alleles tend to follow one another? Mendel paired two traits together and crossed AABB x aabb (F 1 ) The resulting heterozygotes were then allowed to self pollinate (F 2 ) Dihybrid cross 9:3:3:1
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Probability Rules Probability scale – 0-1 1 = event is certain to occur 0 = event is certain not to occur Multiplication rule – used for two or more independent events (Ex. Chance of having 5 boys in a row) ½ x ½x ½ x ½ x ½ = 1/32 Addition rule – used for mutually exclusive events (Ex. Male vs. female) ¼ = ¼ = ½
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Degrees of Dominance Alleles can show different degrees of dominance/recessive Incomplete dominance is when neither allele is completely dominant (blended) Codominance is when two alleles affect the individual in separate, distinguishable ways
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Relationship Between Genotype and Phenotype Alleles can looked at on three phenotipic levels Ex. Tay Sachs disease Only children that inherit two recessive alleles have the disease- organismal level is recessive Heterozygotes produce enough of enzyme to be normal – biochemical level is incomplete dominance Heterozygotes also produce equal numbers of normal and dysfunctional enzymes – molecular level is codomiance
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Multiple Alleles and Pleitropy Some genes exist with multiple alleles Blood type I A, I B, I Also codominance Some genes can have multiple phenotypic effects Responsible for many symptoms associated with many genetic disorders
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Epistasis Phenotypic expression of one gene is affected by another gene Ex. Labs
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Polygenic Inheritance Quantitative characters are the result of polygenic inheritance Multiple genes determining the resulting phenotype Ex. Height, skin color Alleles have a cumulative affect
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Human Traits and Pedigree Geneticists can not manipulate traits in humans To analyze they use a pedigree Using information from family history about a particular trait
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Autosomal Recessive Disorders To get the disorder individual must inherit both recessive alleles Heterozygotes are called carriers When recessive disorders are rare, highly unlikely carriers will meet and mate
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Autosomal Dominant Disorders Individual must inherit only one dominant allele to have the disorder Achondroplasia Huntington’s disease
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Genetic Testing and Counseling Most recessive individuals come from normal parents 9carriers) Problems with knowing? Insurance Loss of jobs Types of testing Amniocentesis Chorionic villus sampling
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Genetic Screening and Testing
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