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Mendel and the Gene Idea
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Monk Pea Plants many varieties, easy to reproduce and control, tracked traits that were “either-or”, started with true breeding plants
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P generation = true breeding parents Purple x White F1 generation = hybrids from P generation cross All purple plants F2 generation = offspring from F1 self- pollination 3:1 ratio of purple to white plants P Generation (true-breeding parents) Purple flowers White flowers F 1 Generation (hybrids) All plants had purple flowers F 2 Generation
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1. Alternate versions of genes ALLELES Found on Homologous Chromosomes Represented with letters Figure 14.4 Allele for purple flowers Locus for flower-color gene Homologous pair of chromosomes Allele for white flowers
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2. Each trait is controlled by 2 alleles – one contributed from each parent
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3. The Law of Segregation The 2 alleles for a trait segregate during gamete formation (meiosis) and end up in different gametes
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Mendel’s Other Law: The Law of Independent Assortment Genes located on different chromosomes are inherited independently Exceptions: genes far away on same chromosome (many map units apart) allowing crossing over to occur can be inherited independently * Genes located close together and are usually inherited together are called “linked” ex: red hair, freckles
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4. Some alleles are dominant while others are recessive Dominant alleles “mask” recessive Dominant alleles = capital letters Recessive alleles = lowercase letters
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Homozygous = 2 of the same alleles Homozygous Dominant = DD Shows dominant trait Homozygous Recessive = dd Shows recessive trait Heterozygous = 1 dominant, 1 recessive allele Heterozygous = Dd Shows dominant trait and masks recessive Genotype = allele make up (ex: DD) Phenotype = physical trait
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Punnett Squares Aka Monohybrid Cross 1 trait Explains Law of Segregation
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Allows us to determine the genotype of an organism with the dominant phenotype, but unknown genotype Is the organism DD or Dd?! Crosses an individual with the dominant phenotype with an individual that is homozygous recessive for a trait
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The testcross Figure 14.7 Dominant phenotype, unknown genotype: PP or Pp? Recessive phenotype, known genotype: pp If PP, then all offspring purple: If Pp, then 1 ⁄ 2 offspring purple and 1 ⁄ 2 offspring white: p p P P Pp pp Pp P p pp APPLICATION An organism that exhibits a dominant trait, such as purple flowers in pea plants, can be either homozygous for the dominant allele or heterozygous. To determine the organism’s genotype, geneticists can perform a testcross. TECHNIQUE In a testcross, the individual with the unknown genotype is crossed with a homozygous individual expressing the recessive trait (white flowers in this example). By observing the phenotypes of the offspring resulting from this cross, we can deduce the genotype of the purple-flowered parent. RESULTS
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Shows inheritance of two traits Ex: seed color AND seed shape Typical Outcome for 2 heterozygous individuals: 9:3:3:1
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Complete Dominance Phenotype of Dd is the same as DD Codominance Shows 2 dominant traits Ex: BB = black, WW = white, BW = black AND white Incomplete Dominance Shows blended pattern Ex: C R C R = Red, C w C w = White, C R C W = Pink
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Most traits are controlled by 2 alleles (ex: DD) Some traits have more than 2 alleles ABO Blood Type I A, I B, i are the 3 alelles Table 14.2
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1 gene has multiple phenotypic effects Ex: Sickle Cell Anemia
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Ex: Hair, Skin, Eye Color Additive Effects AaBbCc aabbcc Aabbcc AaBbccAaBbCcAABbCc AABBCcAABBCC 20 ⁄ 64 15 ⁄ 64 6 ⁄ 64 1 ⁄ 64 Fraction of progeny
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A gene at one locus alters the phenotypic expression of a gene at a second locus (masks the other gene) Ex: Laborador Retrievers 2 genes: (E,e) & (B,b) pigment (E) or no pigment (e) pigment concentration: black (B) to brown (b) Outcome differs from 9:3:3:1
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Controlled by genetics and environment Ex: Skin color in humans, hydrangea color Nature vs. Nurture
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Circles = Females Squares = Males Shaded = Expresses phenotype Half-Shaded = Carriers Parents joined by horizontal lines Offspring listed below parents in birth order
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Most are recessive (require homozygous recessive genotype) Carriers = heterozygous individuals that do not show trait, but “carry” the gene for it (Ex: Aa) Cystic Fibrosis: defective chloride channel in cell membranes lead to build up of thickened mucus Tay-Sach’s disease: brain cells cannot metabolize lipids Sickle-Cell Anemia: misshaped blood cells
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Huntington’s Disease: Dominant, degenerative disease of nervous system Achondroplasia: Dominant form of dwarfism (“AA” is lethal) Many disorders are multifactorial Heart disease Cancer Diabetes
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Fetal Testing Amniocentesis: withdrawl of fluid from amniotic sac to collect cells for viewing and karyotyping Chorionic villus sampling (CVS): small amount of tissue suctioned from placenta Ultrasound: non-invasive, reveals structures Newborn Screening Blood: test for PKU (Phenylketonuria) Recessive disorder that leads to mental retardation Requires a change in diet
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