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UNIT VI - MENDELIAN GENETICS Baby Campbell – Ch 9 Big Campbell – Ch 14, 15 I. MENDEL • Mendel’s Experiments o Worked with ______________ pea plants o Eliminated ________________________ and self-pollination controlled ____________________ cross-pollination o P Generation - True-breeding pea plants with one trait X true-breeding pea plants with another trait o Produced hybrids also known as F1 ___________________________ TT x tt F1 Phenotype = 4 tall : 0 short F1 Genotype = 0 TT : 4 Tt : 0 tt o F1 X F1 → F2 Tt x Tt ___________________________ F2 Phenotype Ratio = 3 tall : 1 short F2 Genotype Ratio = 1 TT : 2 Tt : 1 tt I. MENDEL, cont • Mendel’s Principles 1) 2) 3) 4) 5) Alternative versions of genes known alleles as ______________ account for variations in inherited characters. 2 Organisms inherit _____ alleles for each trait If alleles at a locus differ; that is; if heterozygous the genotype is _______________, the allele that shows is known as the dominant ________________ allele. Law of Segregation – two alleles for a heritable character segregate during meiosis Law of Independent Assortment – each pair of alleles segregates independently of each other pair of alleles during meiosis II. ANALYZING PROBABILITY OF TRAIT INHERITANCE • Test Cross o Organisms with dominant phenotype crossed with _____________________________ homozygous recessive to determine genotype • Punnett Square • Multiplication Rule o States the probability of 2 or more independent events occurring together can calculated by multiplying individual probabilities o For example, Determine the probability of a homozygous recessive short plant produced from F1 X F1 Cross = Tt x Tt Probability of egg carrying t = ½ Probability of sperm carrying t = ½ Probability of tt offspring = ¼ II. ANALYZING PROBABILITIES, cont • Addition Rule o States that the probability of 2 or more mutually exclusive events occurring can be calculated by adding together their individual probabilities o For example, Determine the probability of a heterozygous plant produced from F1 X F1 Tt x Tt Chance of egg carrying T = ½ Chance of sperm carrying t = ½ Chance of sperm carrying T = ½ Chance of egg carrying t = ½ Probability of Tt offspring = ¼ + ¼ = ½ II. ANALYZING PROBABILITIES, cont • Crosses Involving Multiple Characters o Determine the genotype ratios of the offspring for the cross BbDD X BBDd II. ANALYZING PROBABILITIES, cont • Crosses Involving Multiple Characters o Determine the genotype ratios of the offspring for the cross YyRr X YyRr II. ANALYZING PROBABILITIES, cont • Crosses Involving Multiple Characters o In the cross, PpYyRr X Ppyyrr, what is the probability of offspring that are purple, green, & round? P= purple, p = white Y = yellow, y = green R = round, r = wrinkled Probability Practice Makes Perfect! In pea plants, • long stems are dominant to short stems • purple flowers are dominant to white, and • round seeds are dominant to wrinkled. A plant that is heterozygous for all three loci self-pollinates and 2048 progeny are examined. How many of the resulting plants would you expect to be long-stemmed with purple flowers, producing wrinkled seeds? II. ANALYZING PROBABILITIES, cont • Pedigree Analysis Recessive Trait Dominant Trait… III. VARIATIONS IN INHERITANCE • Co-Dominance o Both alleles affect phenotype in separate & distinguishable ways o Often designated with 2 different “big letters” • Incomplete Dominance o Neither allele is dominant; heterozygotes show a blend of two homozygous phenotypes o One allele designated with “big letter’, the other with “big letter prime”; for example T T’ III. VARIATIONS IN INHERITANCE, cont • Multiple Alleles o Many genes have more than 2 alleles o Example, ABO blood groups in humans o Three alleles • A woman with O blood has a child with Type A blood. The man she claims is the father has AB blood. Is it possible that he is the father of this child? Phenotype A B AB O Genotype III. VARIATIONS IN INHERITANCE, cont • Polygenic Inheritance o For example, AABBCC = very dark skin; aabbcc = very light skin. o Intensity based on units; in other words, AaBbCc and AABbcc individuals would have the same pigmentation III. VARIATIONS IN INHERITANCE, cont • Epistasis o Gene at one locus alters phenotypic expression of a gene at a second locus o For example, A dominant allele, P causes the production of purple pigment; pp individuals are white. A dominant allele C is also required for color production; cc individuals are white. What proportion of offspring will be purple from a ppCc x PpCc cross? III. VARIATIONS IN INHERITANCE, cont • Pleiotropy III. VARIATIONS IN INHERITANCE, cont • Environmental Impact on Phenotypes IV. SEX-LINKED INHERITANCE o First recognized by Thomas Hunt Morgan Drosophila melanogaster Fruit flies Excellent organism for genetic studies Prolific breeding habits Simple genetic make-up; 4 pairs of chromosomes → 3 pairs of autosomes, 1 pair of sex chromosomes Crossed true-breeding wild-type females with true-breeding mutant males Mutant trait showed up in ½ male F2 offspring ; was not seen in F2 females o Determined mutant allele was on X-chromosome; thus inherited differently in males versus females In females, In males, IV. SEX-LINKED INHERITANCE, cont • Red-green colorblindness is caused by a sex-linked recessive allele. A colorblind man marries a woman with normal vision whose father was colorblind. What is the probability she will have a colorblind daughter? IV. SEX-LINKED INHERITANCE, cont • The gene for amber body color in Drosophila is sex-linked recessive. The dominant allele produces wild type body color. The gene for black eyes is autosomal recessive; the wild type red eyes are dominant. If males with amber bodies, heterozygous for eye color are crossed with females heterozygous for eye color and body color, calculate the expected phenotype ratios in the offspring. IV. SEX-LINKED INHERITANCE, cont • X Inactivation in Females o During embryonic development, one X chromosome in female cells is inactivated due to addition of methyl group to its DNA o Dosage compensation o Inactive X chromosome condenses; known as Barr body IV. SEX-LINKED IN INHERITANCE, cont o Occurs randomly Females will have some cells where “Dad’s copy” of X is inactivated, some where “Mom’s copy” is inactive Therefore, females are a mosaic of cells Preserved in mitosis In ovaries, Barr body chromosome is reactivated for meiosis and oogenesis IV. SEX-LINKED INHERITANCE, cont • X Inactivation Calico coloration in female cats V. GENE MUTATIONS o Change in the nucleotide sequence o May be spontaneous mistakes that occur during replication, repair, or recombination o May be caused by mutagens; for example, x-rays, UV light, carcinogens o If changes involve long stretches of DNA, known as chromosomal mutations o Point mutations – change in a gene involving a single nucleotide pair; 2 types Substitution Frameshift – due to addition or deletion of nucleotide pairs V. GENE MUTATIONS, cont • Classification of Gene Mutations o Traits may be described as dominant, recessive, etc . based on the effect of the abnormal allele on the organism’s phenotype o Instruction encoded by genes carried out through protein synthesis o Vast majority of proteins are enzymes o Abnormal allele → Defective enzyme If the enzyme produced by the normal allele is present in sufficient quantities to catalyze necessary reactions, No noticeable effect on phenotype Defective allele is classified as recessive If the lack of normal enzyme production by defective allele cannot be overcome by normal allele, Organism’s phenotype is affected Defective allele is classified as dominant VI. INHERITED GENETIC DISORDERS • Due to gene mutations • Classified as autosomal or sex-linked, depending on chromosome location of affected gene • Autosomal Disorders – Grouped according to path of inheritance o Autosomal Recessive Disorders VI. INHERITED GENETIC DISORDERS Albinism VI. INHERITED GENETIC DISORDERS, cont Cystic Fibrosis VI. INHERITED GENETIC DISORDERS, cont PKU VI. INHERITED GENETIC DISORDERS, cont Tay-Sachs VI. INHERITED GENETIC DISORDERS, cont o Autosomal Co-Dominant Disorders Sickle Cell Anemia VI. INHERITED GENETIC DISORDERS, cont o Autosomal Dominant Disorders Huntington’s Disease VI. INHERITED GENETIC DISORDERS, cont • Autosomal Dominant Disorders Marfan Syndrome VI. INHERITED GENETIC DISORDERS, cont • Autosomal Dominant Disorders Achondroplasia VI. INHERITED GENETIC DISORDERS, cont • Hypercholesteremia VI. INHERITED GENETIC DISORDERS, cont • Sex-Linked Disorders o All o Affect o Hemophilia VI. INHERITED GENETIC DISORDERS, cont o Colorblindness o Duchenne Muscular Dystrophy VII. TESTING FOR INHERITED GENETIC DISORDERS • Identification of Carriers/Genetic Counseling o Tests are available for Tay-Sachs, sickle cell, cystic fibrosis, Huntington’s, PKU, & many others • PGD – Preimplantation Genetic Diagnosis VII. GENETIC TESTING, cont • Fetal Testing o Amniocentesis Performed between 14th-16th weeks of pregnancy Cells collected, tested VII. GENETIC TESTING, cont o Chorionic Villus Sampling (CVS) Narrow tube inserted through mother’s vagina, cervix Small tissue sample suctioned from placenta (organ that transmits nutrients, removes wastes from fetus) Testing may be done earlier in pregnancy but not suitable for all types of testing • Newborn Screening o PKU VIII. CHROMOSOMAL BASIS OF INHERITANCE • Chromosomal Theory of Inheritance o States genes occupy specific loci on chromosomes o During meiosis, chromosomes undergo segregation & independent assortment • Linked Genes o During Thomas Morgan’s work with Drosophila, he recognized Two genes located on same chromosome were linked; that is, inherited together However, offspring phenotypes showed this wasn’t always true VIII. CHROMOSOMAL BASIS OF INHERITANCE, cont • Linked Genes, cont o In fruit flies, normal wild-type phenotype is gray body, normal wings – both genes are located on same chromosome G = wild-type (gray) body; g = black body W = wild-type wings; w = mutant wings o True-breeding wild type flies X true-breeding mutants o F1 showed all o F1 X test cross Counted 2300 offspring Should have counted VIII. CHROMOSOMAL BASIS OF INHERITANCE, cont 965 GWgw 944 gwgw 206 Gwgw Morgan realized variation in probabilities due to 185 gWgw VIII. CHROMOSOMAL BASIS OF INHERITANCE, cont • Linkage Maps o In crossing over, the further apart two genes are, the higher the probability that a crossover will occur between them and therefore, the higher the recombination frequency. VIII. CHROMOSOMAL BASIS OF INHERITANCE, cont o Recombination Frequency = # recombinants__ X 100 total # offspring o One map unit = 1% recombination frequency …………………………………………………………………………………….. 965 GWgw 944 gwgw 206 Gwgw 185 gWgw VIII. CHROMOSOMAL BASIS OF INHERITANCE, cont • The genes for vestigial wings, black body color, and cinnabar eyes are linked genes. • In controlled crosses . .. The gene for vestigial (vg) wings and body color (b) have a 17% crossover rate. The gene for eye color (cn) and body color (b) have a 9% crossover rate. The gene for eye color (cn) and vestigial wings (vg) have a 9 ½% crossover rate. • Draw the chromosome. IX. CHROMOSOMAL DISORDERS • Alterations in Chromosome Number o Most commonly due to nondisjunction o Results in aneuploid gametes IX. CHROMOSOMAL DISORDERS, cont IX. CHROMOSOMAL DISORDERS, cont o Detected with karyotype o Examples Down Syndrome IX. CHROMOSOMAL DISORDERS, cont Turner Syndrome IX. CHROMOSOMAL DISORDERS, cont • Klinefelter Syndrome IX. CHROMOSOMAL DISORDERS, cont IX. CHROMOSOMAL DISORDERS, cont • Cri du Chat – Caused by deletion in chromosome 5 • Chronic Myelogenous Leukemia – Caused by reciprocal translocation. Large piece of chromosome 22 exchanges places with tip of chromosome 9. Resulting chromosome 22 easily recognizable; known as Philadelphia chromosome.