Lesson #17 Genetic Information #2

Cards (53)

  • Who proposed the chromosomal theory of inheritance?
    Walter Sutton
  • What did Walter Sutton observe during meiosis?
    Similar chromosomes pair during meiosis
  • What is the chromosomal theory of inheritance?
    Chromosomes are the carriers of genetic information and the basis for genetic inheritance
  • What organism did T.H. Morgan use for his genetic studies?
    Drosophila melanogaster (fruit fly)
  • What was the first mutant trait discovered by T.H. Morgan in fruit flies?
    White eyes instead of red
  • What were the phenotypes of the F1 generation when crossing a mutant male fly with a normal red-eyed female?
    All F1 generation were red-eyed (dominant)
  • What was the result of the F2 generation in the cross of the mutant male fly and the normal female?
    All white-eyed flies were male
  • How is sex determined in Drosophila?
    The number of X chromosomes determines sex
  • What are the common sex chromosomes in many species?
    X and Y chromosomes
  • How do female and male gametes differ in Drosophila during meiosis?
    Female gametes are X, while male gametes are X or Y
  • What determines sex in humans?
    The presence of the Y chromosome
  • What is the structure of the Y chromosome in humans?
    The Y chromosome is highly condensed
  • What is the "default" sex for humans?
    The default is female
  • What gene is required for "maleness" in humans?
    The SRY gene on the Y chromosome
  • What type of trait is white eye color in fruit flies?
    It is a sex-linked (X-linked) trait
  • Name two examples of X-linked traits in humans.
    Hemophilia and colorblindness
  • What are epigenetic mechanisms?
    Regulators of gene function/expression that do not involve a change in the DNA sequence
  • What does the term "epigenetic" refer to?
    It refers to inheritance that is "over and above" genetic inheritance
  • What is dosage compensation?
    It ensures equal expression of genes from the sex chromosome in females and males
  • What happens to one of the X chromosomes in female cells?
    One X chromosome is inactivated and condensed into a Barr body
  • What does it mean for females heterozygous for genes on the X chromosome to be genetic mosaics?
    Different cells express different alleles depending on which X chromosome is inactivated
  • How is fur color in female mammals determined?
    By a gene present on the X chromosome
  • What is genomic imprinting?
    Imprinted genes are inactivated based on which parental line the gene was inherited from
  • How is mitochondrial DNA inherited?
    Mitochondrial DNA is generally inherited from one parent, usually the mother
  • What is maternal inheritance?
    It refers to the inheritance of traits associated with organelle genomes from the mother
  • What is sickle cell anemia caused by?
    A defect in hemoglobin
  • What is the effect of sickle cell anemia on oxygen delivery?
    It leads to impaired oxygen delivery to tissues
  • How do homozygotes and heterozygotes for sickle cell anemia differ in terms of symptoms?
    Homozygotes exhibit illness, while heterozygotes appear normal under normal O2 conditions
  • Why is sickle cell anemia particularly prevalent in people of African descent?
    It confers resistance to the blood-borne parasite that causes malaria
  • What is nondisjunction?
    Failure of homologous or sister chromatids to separate properly during meiosis
  • What does nondisjunction lead to?
    Aneuploidy, which is the gain or loss of a chromosome
  • What is monosomy?
    Chromosome loss
  • What is trisomy?
    Chromosome gain
  • How do aneuploid human embryos typically develop?
    Aneuploid human embryos rarely develop
  • What is Trisomy 21 also known as?
    Down syndrome
  • What factors influence the risk of Trisomy 21?
    The mother's age influences the risk
  • What happens when nondisjunction occurs with sex chromosomes?
    It may cause somewhat abnormal features, but many reach maturity and may be fertile
  • What is Triple X syndrome?
    It occurs when the X chromosome fails to segregate
  • What is Klinefelter syndrome?
    It occurs when there is an extra X chromosome in males
  • What is Turner syndrome?
    It occurs when there is a missing X chromosome in females