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BIOLOGY Chapter 11: pp. 189 - 210 10th Edition Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Parents TT Ee tt Ee t T eggs E e Tt eggs Ee e T t T sperm EE Punnett square E spem Sylvia S. Mader Mendelian Patterns of Inheritance TT Tt Tt tt t Ee Offspring ee Offspring PowerPoint® Lecture Slides are prepared by Dr. Isaac Barjis, Biology Instructor Copyright © The McGraw Hill Companies Inc. Permission required for reproduction or display 1 Outline Blending Inheritance Monohybrid Cross Law of Segregation Modern Genetics Genotype vs. Phenotype Punnett Square Dihybrid Cross Law of Independent Assortment Human Genetic Disorders 2 Gregor Mendel Austrian monk Studied science and mathematics at University of Vienna Conducted breeding experiments with the garden pea Pisum sativum Carefully gathered and documented mathematical data from his experiments Formulated fundamental laws of heredity in early 1860s Had no knowledge of cells or chromosomes Did not have a microscope 3 Gregor Mendel Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. © Ned M. Seidler/Nationa1 Geographic Image Collection 4 Fruit and Flower of the Garden Pea Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Flower Structure stamen anther filament stigma style a. carpel ovules in ovary 5 Garden Pea Traits Studied by Mendel Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Cutting away anthers Brushing on pollen from another plant All peas are yellow when one parent produces yellow seeds and the other parent produces green seeds. 6 Blending Inheritance Theories of inheritance in Mendel’s time: Based on blending Parents of contrasting appearance produce offspring of intermediate appearance Mendel’s findings were in contrast with this He formulated the particulate theory of inheritance Inheritance involves reshuffling of genes from generation to generation 7 One-Trait Inheritance Mendel performed cross-breeding experiments Used “true-breeding” (homozygous) plants Chose varieties that differed in only one trait (monohybrid cross) Performed reciprocal crosses Parental generation = P First filial generation offspring = F1 Second filial generation offspring = F2 Formulated the Law of Segregation 8 Mendel’s Monohybrid Crosses: An Example Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. P generation TT P gametes tt T t F1 generation Tt F1 gametes T t F2 generation sperm T TT Tt Tt tt t Offspring Allele Key T = tall plant t = short plant Phenotypic Ratio 3 1 tall short 9 Law of Segregation Each individual has a pair of factors (alleles) for each trait The factors (alleles) segregate (separate) during gamete (sperm & egg) formation Each gamete contains only one factor (allele) from each pair Fertilization gives the offspring two factors for each trait 10 Modern Genetics View Each trait in a pea plant is controlled by two alleles (alternate forms of a gene) Dominant allele (capital letter) masks the expression of the recessive allele (lower-case) Alleles occur on a homologous pair of chromosomes at a particular gene locus Homozygous = identical alleles Heterozygous = different alleles 11 Homologous Chromosomes Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. sister chromatids alleles at a gene locus a. Homologous chromosomes have alleles for same genes at specific loci. G g R r S s t T G Replication b. Sister chromatids of duplicated chromosomes have same alleles for each gene. R G g g R r r S S s s t t T T 12 Genotype versus Phenotype Genotype Refers to the two alleles an individual has for a specific trait If identical, genotype is homozygous If different, genotype is heterozygous Phenotype Refers to the physical appearance of the individual 13 Genotype versus Phenotype 14 Punnett Square Table listing all possible genotypes resulting from a cross All possible sperm genotypes are lined up on one side All possible egg genotypes are lined up on the other side Every possible zygote genotypes are placed within the squares 15 Punnett Square Allows us to easily calculate probability, of genotypes and phenotypes among the offspring Punnett square in next slide shows a 50% (or ½) chance The chance of E = ½ The chance of e = ½ An offspring will inherit: The chance of EE =½!½=¼ The chance of Ee =½!½=¼ The chance of eE =½!½=¼ The chance of ee =½!½=¼ 16 Punnett Square Showing Earlobe Inheritance Patterns Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Parents Ee Ee eggs E e EE Ee Ee ee Punnett square spem E e Offspring Allele key E = unattached earlobes e = attached earlobes Phenotypic Ratio 3 unattached earlobes 1 attached earlobes 17 Monohybrid Test cross Individuals with recessive phenotype always have the homozygous recessive genotype However, individuals with dominant phenotype have indeterminate genotype May be homozygous dominant, or Heterozygous Test cross determines genotype of individual having dominant phenotype 18 One-Trait Test Cross Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Tt tt Insert figure 11.7a here eggs t sperm Allele Key T = tall plant t = short plant T t Tt Phenotypic Ratio 1 1 tall short tt a. Offspring 19 One-Trait Test Cross Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. TT tt T t eggs sperm Allele Key T = tall plant t = short plant Phenotypic Ratio All tall plants Tt b. Offspring 20 Two-Trait Inheritance Dihybrid cross uses true-breeding plants differing in two traits Observed phenotypes among F2 plants Formulated Law of Independent Assortment The pair of factors for one trait segregate independently of the factors for other traits All possible combinations of factors can occur in the gametes Mendel tracked each trait through two generations. P generation is the parental generation in a breeding experiment. F1 generation is the first-generation offspring in a breeding experiment. F2 generation is the second-generation offspring in a breeding experiment 21 Two-Trait (Dihybrid) Cross Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. P generation TTGG P gametes ttgg tg TG F 1 generation TtGg eggs TG F 1 gametes Tg tG tg TG TTGg TtGG TtGg TTGg TTgg TtGg Ttgg TtGG TtGg ttGG ttGg Ttgg ttGg ttgg Tg sperm F 2 generation TTGG tG tg TtGg Offspring Allele Key T t G g = = = = tall plant short plant green pod yellow pod Phenotypic Ratio 9 3 3 1 tall plant, green pod tall plant, yellow pod short plant, green pod short plant, yellow pod 22 Independent Assortment and Segregation during Meiosis Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. A B A Aa a B Bb b A A B B AB A B a a a b b b ab a b A a B b A A A b b b Ab A Parent cell has two pairs of homologous chromosomes. A Aa a b bB B b a a B B a B aB a B All orientations of homologous chromosomes are possible at metaphase I in keeping with the law of independent assortment. At metaphase II, each daughter cell has only one member of each homologous pair in keeping with the law of segregation. All possible combinations of chromosomes and alleles occur in the gametes as suggested by Mendel's two laws. 23 Animation Please note that due to differing operating systems, some animations will not appear until the presentation is viewed in Presentation Mode (Slide Show view). You may see blank slides in the “Normal” or “Slide Sorter” views. All animations will appear after viewing in Presentation Mode and playing each animation. Most animations will require the latest version of the Flash Player, which is available at http://get.adobe.com/flashplayer. 24 Human Genetic Disorders Genetic disorders are medical conditions caused by alleles inherited from parents Autosome - Any chromosome other than a sex chromosome (X or Y) Genetic disorders caused by genes on autosomes are called autosomal disorders Some genetic disorders are autosomal dominant An individual with AA has the disorder An individual with Aa has the disorder An individual with aa does NOT have disorder Other genetic disorders are autosomal recessive An individual with AA does NOT have disorder An individual with Aa does NOT have disorder, but is a carrier An individual with aa DOES have the disorder 25 Autosomal Recessive Pedigree Chart Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. I II III IV aa A? A? Aa Aa Aa * Aa aa aa A? A? A? A? Key aa = affected Aa = carrier (unaffected) AA = unaffected A? = unaffected Autosomal recessive disorders (one allele unknown) • Most affected children have unaffected parents. • Heterozygotes (Aa) have an unaffected phenotype. • Two affected parents will always have affected children. • Close relatives who reproduce are more likely to have affected children. • Both males and females are affected with equal frequency. 26 Autosomal Dominant Pedigree Chart Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Aa Aa I * II III Aa aa Aa Aa aa A? aa aa aa aa aa aa Key AA = affected Aa = affected A? = affected (one allele unknown) aa = unaffected Autosomal dominant disorders • affected children will usually have an affected parent. • Heterozygotes (Aa) are affected. • Two affected parents can produce an unaffected child. • Two unaffected parents will not have affected children. • Both males and females are affected with equal frequency. 27 Autosomal Recessive Disorders Tay-Sachs Disease Cystic Fibrosis Progressive deterioration of psychomotor functions Mucus in bronchial tubes and pancreatic ducts is particularly thick and viscous Phenylketonuria (PKU) Lack enzyme for normal metabolism of phenylalanine 28 Cystic Fibrosis Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. H2O Cl- Cl- ClCl- H2O H2O Cl- nebulizer defective channel percussion vest thick mucus © Pat Pendarvis 29 Methemoglobinemia Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Courtesy Division of Medical Toxicology, University of Virginia 30 Animation Please note that due to differing operating systems, some animations will not appear until the presentation is viewed in Presentation Mode (Slide Show view). You may see blank slides in the “Normal” or “Slide Sorter” views. All animations will appear after viewing in Presentation Mode and playing each animation. Most animations will require the latest version of the Flash Player, which is available at http://get.adobe.com/flashplayer. Autosomal Dominant Disorders Neurofibromatosis Tan or dark spots develop on skin and darken Small, benign tumors may arise from fibrous nerve coverings Huntington Disease Neurological disorder Progressive degeneration of brain cells Severe muscle spasms Personality disorders 32 A Victim of Huntington Disease Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. JK JJ JK JL JK JL KL a. JL JK JK JL JL JL JJ KL JJ KL JJ KL JJ JK JK JK JK KL JK JK KL KK KL JL JJ KL KL KL b. a: © Steve Uzzell 33 Incomplete Dominance Heterozygote has phenotype intermediate between that of either homozygote Homozygous red has red phenotype Homozygous white has white phenotype Heterozygote has pink (intermediate) phenotype Phenotype reveals genotype without test cross 34 Incomplete Dominance Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. R1R2 R1R2 eggs R1 R2 sperm R1 R1R1 R1R2 R2 R1R2 R2R2 Key 1 R1R1 2 R1R2 1 R2R2 red pink white Offspring 35 Multiple Allelic Traits Some traits controlled by multiple alleles The gene exists in several allelic forms (but each individual only has two) ABO blood types The alleles: IA = A antigen on red cells, anti-B antibody in plasma IB = B antigen on red cells, anti-AB antibody in plasma I = Neither A nor B antigens, both antibodies 36 Multiple Allelic Traits 37 Pleioptropic Effects Pleiotropy occurs when a single mutant gene affects two or more distinct and seemingly unrelated traits. Marfan syndrome have disproportionately long arms, legs, hands, and feet; a weakened aorta; poor eyesight 38 Marfan Syndrome Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Connective tissue defects Skeleton Heart and blood vessels Chest wall deformities Mitral valve Long, thin fingers, arms, legs prolapse Scoliosis (curvature of the spine) Flat feet Long, narrow face Loose joints Enlargement of aorta Eyes Lens dislocation Severe nearsightedness Aneurysm Aortic wall tear Lungs Collapsed lungs Skin Stretch marks in skin Recurrent hernias Dural ectasia: stretching of the membrane that holds spinal fluid (Left): © AP/Wide World Photos; (Right): © Ed Reschke 39 Polygenic Inheritance Occurs when a trait is governed by two or more genes having different alleles Each dominant allele has a quantitative effect on the phenotype These effects are additive Result in continuous variation of phenotypes 40 Frequency Distributions in Polygenic Inheritance Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. P generation F1 generation F2 generation Proportion of Population 20 — 64 15 — 64 6 — 64 1 — 64 Genotype Examples 41 X – Linked Inheritance In mammals The X and Y chromosomes determine gender Females are XX Males are XY The term X-linked is used for genes that have nothing to do with gender Carried on the X chromosome. The Y chromosome does not carry these genes Discovered in the early 1900s by a group at Columbia University, headed by Thomas Hunt Morgan. Performed experiments with fruit flies They can be easily and inexpensively raised in simple laboratory glassware Fruit flies have the same sex chromosome pattern as humans 42 X – Linked Inheritance Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. P generation XrY P gametes Xr XRXR XR Y F1 generation XRY XRXr eggs XR F1 gametes Xr F2 generation sperm XR XRXR XRXr XRY XrY Y Offspring Allele Key XR = red eyes Xr = white eyes Phenotypic Ratio females: males : 1 1 all red-eyed red-eyed white-eyed 43 Human X-Linked Disorders Several X-linked recessive disorders occur in humans: Color blindness Menkes syndrome Wasting away of the muscle Adrenoleukodystrophy Caused by a defective allele on the X chromosome Disrupts movement of the metal copper in and out of cells. Muscular dystrophy The allele for the blue-sensitive protein is autosomal The alleles for the red- and green-sensitive pigments are on the X chromosome. X-linked recessive disorder Failure of a carrier protein to move either an enzyme or very long chain fatty acid into peroxisomes. Hemophilia Absence or minimal presence of a clotting factor VIII, or clotting factor IX Affected person’s blood either does not clot or clots very slowly. 44 X-Linked Recessive Pedigree Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. XbY XBXB XBY XBXb daughter grandfather XBY XbXb XbY XBY XBXB XBXb XbY grandson XBXB XBXb XbXb XbY XbY Key = Unaffected female = Carrier female = Color-blind female = Unaffected male = Color-blind male X-Linked Recessive Disorders • More males than females are affected. • An affected son can have parents who have the normal phenotype. • For a female to have the characteristic, her father must also have it. Her mother must have it or be a carrier. • The characteristic often skips a generation from the grandfather to the grandson. • If a woman has the characteristic, all of her sons will have it. 45 Muscle Dystrophy Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. fibrous tissue abnormal muscle normal tissue (Abnormal): Courtesy Dr. Rabi Tawil, Director, Neuromuscular Pathology Laboratory, University of Rochester Medical Center; (Boy): Courtesy Muscular Dystrophy Association; (Normal): Courtesy Dr. Rabi Tawil, Director, Neuromuscular Pathology Laboratory, University of Rochester Medical Center. 46 Terminology Pleiotropy Codominance A gene that affects more than one characteristic of an individual Sickle-cell (incomplete dominance) More than one allele is fully expressed ABO blood type (multiple allelic traits) Epistasis A gene at one locus interferes with the expression of a gene at a different locus Human skin color (polygenic inheritance) 47 Review Blending Inheritance Monohybrid Cross Modern Genetics Genotype vs. Phenotype Punnett Square Dihybrid Cross Law of Segregation Law of Independent Assortment Human Genetic Disorders 48 BIOLOGY Chapter 11: pp. 189 - 210 10th Edition Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Parents TT Ee tt Ee t T eggs E e Tt eggs Ee e T t T sperm EE Punnett square E spem Sylvia S. Mader Mendelian Patterns of Inheritance TT Tt Tt tt t Ee Offspring ee Offspring PowerPoint® Lecture Slides are prepared by Dr. Isaac Barjis, Biology Instructor Copyright © The McGraw Hill Companies Inc. Permission required for reproduction or display 49