Definitions:
• Sex-linked
                             Ch. 15 Warm-Up
  gene       1. A white-eyed female fruit-fly is mated with a red-
• Barr body     eyed male. What genotypes and phenotypes do you
• SRY gene      predict for the offspring?
• Linked
  genes      1. Neither Tim nor Rhoda has Duchenne muscular
• Linkage       dystrophy (X-linked recessive disorder), but their
  map           firstborn son has it. What is the probability their 2nd
                child will have it?
               1. Colorblindness is a sex-linked recessive trait. A
                  colorblind male and a female with normal vision
                  have a son who is colorblind. What are the parents’
                  genotypes?
                     Warm up
1. What is a Barr body?
2. How are linkage maps constructed? (See. Fig. 15.11
   in Campbell 9th ed.)
3. Determine the sequence of genes along a
   chromosome based on the following recombination
   frequencies: A-B, 8 map units; A-C, 19 map units; A-
   D, 20 map units; B-C, 11 map units; B-D, 28 map
   units.
4. What does a frequency of recombination of 50%
   indicate?
                     Warm-Up
1. What is the pattern of inheritance of the trait (shaded
   square/circle) shown in the pedigree?
1. How many chromosomes are in a human cell that is:
     a) Diploid? b) Triploid?
     c) Monosomic? d) Trisomic?
THE CHROMOSOMAL BASIS OF
       INHERITANCE
       CHAPTER 15
         What you must know:
• How the chromosome theory of inheritance
  connects the physical movement of chromosomes
  in meiosis to Mendel’s laws of inheritance.
• The unique pattern of inheritance in sex-linked
  genes.
• How alteration of chromosome number or
  structurally altered chromosomes (deletions,
  duplications, etc.) can cause genetic disorders.
• How genetic imprinting and inheritance of
  mitochondrial DNA are exceptions to standard
  Mendelian inheritance.
Chromosome theory of inheritance:
• Genes have specific
  locations (loci) on
  chromosomes
• Chromosomes
  segregate and assort
  independently
                 Chromosomes tagged to reveal a specific gene (yellow).
Thomas Hunt Morgan
• Drosophila melanogaster – fruit fly
  – Fast breeding, 4 prs. chromosomes (XX/XY)
• Sex-linked gene: located on X or Y
  chromosome
  – Red-eyes = wild-type; white-eyes = mutant
  – Specific gene carried on specific chromosome
Sex determination
 varies between
     animals
    Sex-linked genes
• Sex-linked gene on X or Y
• Females (XX), male (XY)
   – Eggs = X, sperm = X or Y
• Fathers pass X-linked genes to daughters, but not
  sons
• Males express recessive trait on the single X
  (hemizygous)
• Females can be affected or carrier
Transmission of sex-linked recessive traits
         Sex-linked disorders
• Colorblindness
• Duchenne muscular dystrophy
• Hemophilia
                       X-Inactivation
    Barr body = inactive X chromosome; regulate gene dosage
    in females during embryonic development
•    Cats: allele for fur
     color is on X
•    Only female cats can
     be tortoiseshell or
     calico.
           Human development
•   Y chromosome required for development of testes
•   Embryo gonads indifferent at 2 months
•   SRY gene: sex-determining region of Y
•   Codes for protein that regulates other genes
Genetic Recombination: production of offspring
with new combo of genes from parents
• If offspring look like parents  parental types
• If different from parents  recombinants
• If results do not follow Mendel’s Law of Independent
  Assortment, then the genes are probably linked
Linked genes: located on same chromosome and
tend to be inherited together during cell division
Crossing over: explains why some linked genes
get separated during meiosis
• the further apart 2 genes on same chromosome,
  the higher the probability of crossing over and
  the higher the recombination frequency
Calculating recombination frequency
Linkage Map: genetic map that is based on
% of cross-over events
• 1 map unit = 1% recombination frequency
• Express relative distances along chromosome
• 50% recombination = far apart on same chromosome
  or on 2 different chromosomes
Exceptions to Mendelian
      Inheritance
            Genomic Imprinting
• Genomic imprinting: phenotypic effect of gene
  depends on whether from M or F parent
• Methylation: silence genes by adding methyl groups
  to DNA
               Non-Nuclear DNA
• Some genes located in
  organelles
   – Mitochondria, chloroplasts,
     plastids
   – Contain small circular DNA
• Mitochondria = maternal
  inheritance (eggs)
               Variegated (striped or spotted) leaves result from mutations in
                pigment genes in plastids, which generally are inherited from
                                                         the maternal parent.
            Genetic Testing
Reasons for Genetic Tests:
•Diagnostic testing (genetic disorders)
•Presymptomatic & predictive testing
•Carrier testing (before having children)
•Pharmacogenetics (medication & dosage)
•Prenatal testing
•Newborn screening
•Preimplantation testing (embryos)
            Prenatal Testing
• May be used on a fetus to detect genetic
  disorders
• Amniocentesis: remove amniotic fluid
  around fetus to culture for karyotype
• Chorionic villus sampling: insert narrow tube
  in cervix to extract sample of placenta with
  fetal cells for karyotype
Nondisjunction:
Nondisjunction chromosomes fail to separate
properly in Meiosis I or Meiosis II
Karyotyping can detect nondisjunctions.
    Down Syndrome = Trisomy 21
        Nondisjunction
Klinefelter Syndrome: 47XYY, 47XXY
   Nondisjunction
Turner Syndrome = 45XO
Chromosomal Mutations
Chromosomal Mutations
Nondisjunction
• Aneuploidy: incorrect # chromosomes
   – Monosomy (1 copy) or Trisomy (3 copies)
• Polyploidy: 2+ complete sets of chromosomes;
  3n or 4n
   – Rare in animals, frequent in plants
 A tetraploid mammal. Scientists think this species may have arisen when an
 ancestor doubled its chromosome # by errors in mitosis or meiosis.
              Review Questions
1. What is the pattern of inheritance of the trait (shaded
   square/circle) shown in the pedigree?
1. How many chromosomes are in a human cell that is:
     a) Diploid? b) Triploid?
     c) Monosomic? d) Trisomic?
      Chi-Square Analysis Practice
• Two true-breeding Drosophila are crossed: a normal-winged,
  red-eyed female and a miniature-winged, vermillion-eyed
  male. The F1 offspring all have normal wings and red eyes.
  When the F1 offspring are crossed with miniature-winged,
  vermillion-eyed flies, the following offspring resulted:
   – 233 normal wing, red eye
   – 247 miniature wing, vermillion eye
   – 7 normal wing, vermillion eye
   – 13 miniature wing, red eye
• What type of conclusions can you draw from this experiment?
  Explain your answer.