midterms gen bio (3rd quarter)

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  • Non-Mendelian Genetics refers to traits that are not aligned with Mendel's law
  • In the 20th century, geneticists learned that the patterns of inheritance were more complicated than what Mendel had discovered
  • Characteristics of Non-Mendelian Genetics
    • When alleles are not completely dominant or recessive
    • A gene has more than 2 allele
    • A gene produces multiple phenotypes
  • Complete Dominance
    One allele has completely dominated the other, following Gregor Mendel's hypothesis
  • Incomplete Dominance
    Neither of the alleles is completely dominant over the other, resulting in an intermediate phenotype ("blending hypothesis")
  • Incomplete Dominance
    • Curly hair (C) is incompletely dominant to straight hair (S), resulting in wavy hair (CS) in the offspring
  • Codominance
    Both alleles are fully expressed, resulting in a phenotype that is a combination of the two
  • Epistasis
    • One gene masks or modifies the expression of another gene
  • Polygenic Inheritance

    • A single phenotypic trait is influenced by multiple genes
  • Nature
    Genetic factors that influence an organism's traits
  • Nurture
    Environmental factors that influence an organism's traits
  • Incomplete dominance
    Neither of the alleles is completely dominant over the other, resulting in an intermediate phenotype
  • Incomplete dominance
    • Curly hair (C) is incompletely dominant to straight hair (S)
  • Incomplete dominance example
    An individual with curly hair is crossed with a straight haired individual, resulting in an offspring with wavy hair
  • Codominance
    Two different alleles are simultaneously expressed in a heterozygous individual
  • Codominance
    • Blood type, where an individual with homozygous type A blood crossed with homozygous type B blood results in offspring with type AB blood
  • Epistasis
    One gene affects the outcome trait of another because of their interaction, where an allele of one gene hides the phenotype of another gene
  • Epistasis
    • Coat color of golden retrievers, where the gene for black/brown pigment is hidden by the recessive allele for white pigment
  • Polygenic inheritance
    Two or more genes affect the expression of a trait, resulting in a phenotypic spectrum
  • Polygenic inheritance
    • Height and skin color
  • Nature
    Innate biological heredity inherited from parents at birth, such as eye color, hair color, height, and genetic diseases
  • Nurture
    Environmental factors that influence an individual's characteristics, such as parenting styles, culture, social relationships, soil acidity, humidity, and sun exposure
  • Mendel's "hereditary factors" were genes
  • Mitosis and meiosis were first described in the late 1800s
  • Locus/Loci
    Specific locations of genes in chromosomes
  • Chromosomes undergo segregation and independent assortment
  • The behavior of chromosomes during meiosis can account for Mendel's laws of segregation and independent assortment
  • Fruit flies
    • Produce many offspring, have a generation every two weeks, and have only four pairs of chromosomes, making them a convenient organism for genetics studies
  • Morgan's experiments with fruit flies provided convincing evidence that chromosomes are the location of Mendel's heritable factors
  • Mutant phenotypes
    Traits alternative to the wild type
  • Morgan's findings on white-eyed mutant allele
    It must be located on the X chromosome
  • Sex chromosomes
    In humans and other mammals, there are two varieties: a larger X chromosome and a smaller Y chromosome
  • SRY gene

    Located on the Y chromosome, codes for a protein that directs the development of male anatomical features
  • Sex-linked genes

    Genes located on either sex chromosome
    1. linked genes
    Genes located on the X chromosome
    1. linked recessive traits

    For a recessive X-linked trait to be expressed, a female needs 2 copies of the allele (homozygous), while a male needs only 1 copy (hemizygous)
    1. linked recessive disorders

    • Color blindness, Duchenne muscular dystrophy, Hemophilia
  • X inactivation
    In mammalian females, one of the two X chromosomes in each cell is randomly inactivated during embryonic development, resulting in a Barr body
  • If a female is heterozygous for a particular gene located on the X chromosome, she will be a mosaic for that character
  • Morgan's experiments with fruit flies showed that body color and wing size are usually inherited together in specific combinations (parental phenotypes), indicating that these genes are on the same chromosome