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Chapter 14 Mendel and the Gene Idea
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Genetics u The scientific study of inheritance. u Genetics is a relatively “new” science (about 150 years).
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Genetic Theories 1. Blending Theory - traits were like paints and mixed evenly from both parents. 2. Incubation Theory - only one parent controlled the traits of the children. Ex: Spermists and Ovists
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3. Particulate Model - parents pass on traits as discrete units that retain their identities in the offspring.
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Gregor Mendel u Father of Modern Genetics.
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u Mendel was a pea picker. u He used peas as his study organism.
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Why Use Peas? u Short life span. u Bisexual. u Many traits known. u Cross- and self-pollinating. u (You can eat the failures).
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Cross-pollination u Two parents. u Results in hybrid offspring where the offspring may be different than the parents.
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Self-pollination u One flower as both parents. u Natural event in peas. u Results in pure-bred offspring where the offspring are identical to the parents.
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Mendel's Work u Used seven characters, each with two expressions or traits. u Example: u Character - height u Traits - tall or short.
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Monohybrid or Mendelian Crosses u Crosses that work with a single character at a time. Example - Tall X short
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P Generation u The Parental generation or the first two individuals used in a cross. Example - Tall X short u Mendel used reciprocal crosses, where the parents alternated for the trait.
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Offspring u F1 - first filial generation. u F2 - second filial generation, bred by crossing two F1 plants together or allowing a F1 to self-pollinate.
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Results - Summary In all crosses, the F1 generation showed only one of the traits regardless of which was male or female. u The other trait reappeared in the F2 at ~25% (3:1 ratio).
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Mendel's Hypothesis 1. Genes can have alternate versions called alleles. 2. Each offspring inherits two alleles, one from each parent.
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Mendel's Hypothesis 3. If the two alleles differ, the dominant allele is expressed. The recessive allele remains hidden unless the dominant allele is absent. Comment - do not use the terms “strongest” to describe the dominant allele.
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Mendel's Hypothesis 4. The two alleles for each trait separate during gamete formation. This now called: Mendel's Law of Segregation
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Law of Segregation
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Mendel’s Experiments u Showed that the Particulate Model best fit the results.
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Vocabulary u Phenotype - the physical appearance of the organism. u Genotype - the genetic makeup of the organism, usually shown in a code. u T = tall u t = short
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Helpful Vocabulary u Homozygous - When the two alleles are the same (TT/tt). u Heterozygous- When the two alleles are different (Tt).
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Test Cross u Cross of a suspected heterozygote with a homozygous recessive. u Ex: T_ X tt If TT - all dominant If Tt - 1 Dominant: 1 Recessive
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Dihybrid Cross u Cross with two genetic traits. u Need 4 letters to code for the cross. u Ex: TtRr u Each Gamete - Must get 1 letter for each trait. u Ex. TR, Tr, etc.
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Number of Kinds of Gametes u Critical to calculating the results of higher level crosses. u Look for the number of heterozygous traits.
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Equation The formula 2 n can be used, where “n” = the number of heterozygous traits. Ex: TtRr, n=2 2 2 or 4 different kinds of gametes are possible. TR, tR, Tr, tr
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Dihybrid Cross TtRr X TtRr Each parent can produce 4 types of gametes. TR, Tr, tR, tr Cross is a 4 X 4 with 16 possible offspring.
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Results u 9 Tall, Red flowered u 3 Tall, white flowered u 3 short, Red flowered u 1 short, white flowered Or: 9:3:3:1
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Law of Independent Assortment u The inheritance of 1st genetic trait is NOT dependent on the inheritance of the 2 nd trait. u Inheritance of height is independent of the inheritance of flower color.
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Comment #1 u Ratio of Tall to short is 3:1 u Ratio of Red to white is 3:1 u The cross is really a product of the ratio of each trait multiplied together. (3:1) X (3:1)
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Probability u Genetics is a specific application of the rules of probability. u Probability - the chance that an event will occur out of the total number of possible events.
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Genetic Ratios u The monohybrid “ratios” are actually the “probabilities” of the results of random fertilization. Ex: 3:1 75% chance of the dominant 25% chance of the recessive
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Rule of Multiplication u The probability that two alleles will come together at fertilization, is equal to the product of their separate probabilities.
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Example: TtRr X TtRr u The probability of getting a tall offspring is ¾. u The probability of getting a red offspring is ¾. u The probability of getting a tall red offspring is ¾ x ¾ = 9/16
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Comment u Use the Product Rule to calculate the results of complex crosses rather than work out the Punnett Squares. u Ex: TtrrGG X TtRrgg
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Solution “T’s” = Tt X Tt = 3:1 (Tall:Short) “R’s” = rr X Rr = 1:1 (Red:White) “G’s” = GG x gg = 1:0 (Yellow:green) Product is: (3:1) X (1:1) X (1:0 ) = 3:3:1:1 Tall, Red, Green peas (3x1x0)
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Variations on Mendel 1. Incomplete Dominance 2. Codominance 3. Multiple Alleles 4. Sex-Linked 5. Polygenic Inheritance
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Incomplete Dominance u When the F1 hybrids show a phenotype somewhere between the phenotypes of the two parents. Ex. Red X White snapdragons F1 = all pink F2 = 1 red: 2 pink: 1 white
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Result u No hidden Recessive. u 3 phenotypes and 3 genotypes u Red = C R C R u Pink = C R C W u White = C W C W
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Codominance u Both alleles are expressed equally in the phenotype. u Ex. Sickle Cell Anemia u AA=Normal blood cells u AA’=Some normal some sickle u A’A’= All Sickle shaped
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Result u No hidden Recessive. u 3 phenotypes and 3 genotypes
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Multiple Alleles u When there are more than 2 alleles for a trait. u Ex. ABO blood group u I A - A type antigen u I B - B type antigen u i - no antigen
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Result u Multiple genotypes and phenotypes. u Very common event in many traits.
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Alleles and Blood Types Type Genotypes A I A I A or I A i B I B I B or I B i AB I A I B O ii
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Comment u Rh blood factor is a separate factor from the ABO blood group. u Rh+ = dominant u Rh- = recessive u A+ blood = dihybrid trait
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Linked genes u There are many genes, but only a few chromosomes. u Therefore, each chromosome must carry a number of genes together as a “package”.
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Linked Genes u Traits that are located on the same chromosome. u Result: u Failure of Mendel's Law of Independent Assortment. u Ratios mimic monohybrid crosses.
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Crossing-Over u Breaks up linkages and creates new ones. u Recombinant offspring formed that doesn't match the parental types.
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If Genes are Linked: u Independent Assortment of traits fails. u Linkage may be “strong” or “weak”.
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Linkage Strength u Degree of strength related to how close the traits are on the chromosome. u Weak - farther apart u Strong - closer together
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u End of part 1
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Chromosomal Basis of Sex in Humans u X chromosome - medium sized chromosome with a large number of traits. u Y chromosome - much smaller chromosome with only a few traits.
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Human Chromosome Sex u Males - XY Females - XX u Comment - The X and Y chromosomes are a homologous pair, but only for a small region at one tip.
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Sex Linkage u Inheritance of traits on the sex chromosomes. u X- Linkage (common) u Y- Linkage (very rare if exists at all)
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Males u Hemizygous - 1 copy of X chromosome. u Show ALL X traits (dominant or recessive). u More likely to show X recessive gene problems than females.
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X-linked Disorders u Color blindness u Duchenne's Muscular Dystrophy u Hemophilia (types a and b) u Immune system defects
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X-linked Patterns u Trait is usually passed from a carrier mother to 1/2 of sons. u Affected father has no affected children, but passes the trait on to all daughters who will be carriers for the trait.
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Can Females be color-blind? u Yes, if their mother was a carrier and their father is affected.
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Sex Limited Traits u Traits that are only expressed in one sex. u Ex – prostate
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Sex Influenced Traits u Traits whose expression differs because of the hormones of the sex. u These are NOT on the sex chromosomes. u Ex. – beards, mammary gland development, baldness
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Polygenic Inheritance u Factors that are expressed as continuous variation. u Lack clear boundaries between the phenotype classes. u Ex: skin color, height
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Genetic Basis u Several genes govern the inheritance of the trait. u Ex: Skin color is likely controlled by at least 4 genes. Each dominant gives a darker skin.
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Result u Mendelian ratios fail. u Traits tend to "run" in families. u Offspring often intermediate between the parental types. u Trait shows a “bell-curve” or continuous variation.
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Genetic Studies in Humans u Often done by Pedigree charts. u Why? u Can’t do controlled breeding studies in humans. u Small number of offspring. u Long life span.
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Pedigree Chart Symbols Male Female Person with trait
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Sample Pedigree
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Dominant Trait Recessive Trait
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Human Recessive Disorders u Several thousand known: u Albinism u Sickle Cell Anemia u Tay-Sachs Disease u Cystic Fibrosis u PKU u Galactosemia
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Sickle-cell Disease u Most common inherited disease among African-Americans. u Single amino acid substitution results in malformed hemoglobin. u Reduced O 2 carrying capacity. u Codominant inheritance.
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Recessive Pattern u Usually rare. u Skips generations. u Occurrence increases with inbred matings.
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Human Dominant Disorders u Less common then recessives. u Ex: u Huntington’s disease u Achondroplasia u Familial Hypercholsterolemia
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Inheritance Pattern u Each affected individual had one affected parent. u Doesn’t skip generations. u Homozygous cases show worse phenotype symptoms. u May have post-maturity onset of symptoms.
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General Formal R = F X M X D R = risk F = probability that the female carries the gene. M = probability that the male carries the gene. D = Disease risk under best conditions.
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Example u Wife has an albino parent. u Husband has no albinism in his pedigree. u Risk for an albino child?
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Risk Calculation u Wife = probability is 1.0 that she has the allele. u Husband = with no family record, probability is near 0. u Disease = this is a recessive trait, so risk is Aa X Aa =.25 u R = 1 X 0 X.25 u R = 0
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Risk Calculation u Assume husband is a carrier, then the risk is: R = 1 X 1 X.25 R =.25 There is a.25 chance that any child will be albino.
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