BIOL 3451 1st Edition Lecture 5Outline of Last Lecture 4.1 Alleles alter phenotypes in Different ways4.2 Geneticists use a variety of symbols for alleles4.3 Neither allele is dominant in imcomplete, or partial dominance4.4 Codominance4.5 Multiple alleles of a gene may exist in a population4.6 Lethal alleles represent essential genes4.7 Combinations of two gene pairs with two modes of inheritance modify the 9:3:3:1 ratioOutline of Current Lecture 4.8 Phenotypes are often affected by more than one gene4.9 Complementation analysis4.10 Expression of a single gene may have multiple effects4.11 X-linkage describes genes on the X chromosome4.12 ln sex-linked and sex-influenced inheritancem an individual’s sex influences the phenotype4.13 Genetic background and the environment may alter phenotypic expressionCurrent Lecture4.8 Phenotypes are often affected by more than one gene Gene interaction: several genes influence a particular characteristic. Doesn’t mean that it can be apply to all genes. Ex: eye development Epigenisis: each step of development increase the complexity of the organ or feature of interest and is controlled by many genes.Epistasis Expression of one gene pair masks or modifies the effect of another gene pair. Look example in the Book!Novel PhenotypesThese notes represent a detailed interpretation of the professor’s lecture. GradeBuddy is best used as a supplement to your own notes, not as a substitute. F2 generation will have a 9:6:1 ratio Example or gene interaction because 2 genes influence the fruit shape equally. Another exemple is the eye color in Drosophila melanogaster Ommatidia: individual visual units that make up compound eye4.9 Complementation analysis Complementation analysis: allow us to determine if 2 independently isolated mutations are in the same gene (alleles) or if they represent mutations in separate genes. Used to screen if any number of mutation will end up giving the same phenotype. Complementation group: all mutations are present in any single gene With this technique, it is possible to predict the total number of genes involved in the determination of that trait.4.10 Expression of a single gene may have multiple effects Marfan syndrome: human disease that result from autosomal dominant mutation in he gene encoding the connective tissue protein fibillin. Porphyria variegata: people who has this can’t adequately metabolize the porphyrin component of hemoglobin when this respiratory pigment is broken down as red blood cells are replaced. Most of the mutations when expressed manifest more than a single time.4.11 X-linkage describes genes on the X chromosome White eyes mutations in Drosophila. Red eyes wild type is dominant to white color. White locus is present on the X chromosome, not Y. Both the gene and the trait is X-linked. Homozygous mother pass it to ALL of their sons, but not all of their daughter. Chromosome theory of inheritance: thecorrelation between Mendel’s work and thebehavior of chromosomes during meiosis. X-linked in human: they can observe easilybecause of the criss-cross in the pedigree. Ex: Color blindness. Duchenne muscular dystrophy: onset before 6 years old, lethal around 20. Normally occurs in males.4.12 ln sex-linked and sex-influenced inheritance an individual’s sex influences the phenotype Doesn’t matter if on X or Y chromosome, some expression of the phenotype only express in a certain sex. (sex-limited inheritance) Expression are modified by the individual’s sex hormones. Another example of a sex-limited inheritance is the breast milk.4.13 Genetic background and the environment may alter phenotypic expressionPenetrance and Expressivity De degree of expression of the gene can be determined by penetrance and expressivity Ex: If 15% of flies with a given mutant genotype show the wild-type appearance, the mutant gene is said to have a penetrance of 85%. Expressivity reflects the range of expression of the mutant genotype.Genetic Background: Positive Effects. The actual location of the gene can depend on where it is in relation to other geneticmaterial. Heterochromatin: if a gene is relocated to OR near certain areas of the chromosome that are condensed and genetically inert.Temperature effects – An Introduction to Conditional Mutations Phenotype can be influenced by the temperature They are called temperature-sensitive mutations Conditional mutation: phenotype expression depends on environmental conditionsNutritional Effects Phenotype doesn’t always reflect the genotype. Ex: mutation in biosynthetic pathway Ex: Phenylketonuria: cant metabolize the amino acid phenylalanine Ex: Galactosemia: can’t metabolize galactose Ex: Lactose intolerance: can’t metabolize lactoseOnset of Genetic Expression Tsay-Sachs disease Lesch-Nyhan syndrome Duchenne muscular dystrophy (DMD) Huntington diseaseGenetic Anticipation Genetic anticipation: Become more severe when passing on to future generations Myotonic dystrophy: most common dystrophy muscular in
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