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The Chromosomal Basis of Inheritance

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The Chromosomal Basis of Inheritance Chapter 15 Biology Campbell Reece Chromosome Theory Chromosome Theory of Inheritance Mendelian genes have specific loci ... – PowerPoint PPT presentation

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Title: The Chromosomal Basis of Inheritance


1
The Chromosomal Basis of Inheritance
  • Chapter 15
  • Biology Campbell Reece

2
Chromosome Theory
  • Chromosome Theory of Inheritance
  • Mendelian genes have specific loci on chromosomes
  • It is the chromosomes that undergo segregation
    and independent assortment
  • Thomas Hunt Morgan was the first to associate a
    specific gene with a specific chromosome

3
Linked Genes
  • Genes located on the sex chromosome are called
    sex-linked genes
  • Ex. Baldness, color-blindness, hemophilia
  • Linked genes genes located on the same
    chromosome tend to be inherited together
  • This violates Mendels Law of Independent
    Assortment, because it is the chromosomes that
    separate, not the genes

4
Colorblindness Test
5
Sex-Linked Genes
  • Tend to be found more often on the X chromosome
    (because it is larger)
  • Therefore, men tend to show sex-linked traits
    more because they only have one X
  • If the trait is caused by a recessive gene, a
    male only requires the one X to have the trait,
    but a female must have the trait on both Xs

6
Gene Mapping
  • Genetic map an ordered list of the genetic loci
    along a particular chromosome
  • The farther apart two genes are on a chromosome,
    the more likely it is that crossing over will
    occur between them
  • Using the recombination frequencies, you can
    calculate the distance (in map units) between
    genes on a chromosome

7
Gene Mapping
8
Alterations of Chromosome Number
  • Nondisjunction the homologous chromosomes fail
    to separate properly during meiosis
  • Aneuploidy an abnormal number of chromosomes
  • Trisomic have 3 copies of a chromosome
  • Monosomic have only 1 copy of a chromosome (the
    other is missing)

9
Alterations of Chromosome Structure
  • Deletion a piece of the chromosome is missing
  • Duplication an extra copy of a segment of the
    chromosome
  • Inversion a reverse segment within a chromosome
  • Translocation a piece from one chromosome
    attaches to a nonhomologous chromosome

10
Alterations of Chromosome Structure
11
Chromosomal Disorders
  • Down Syndrome (Trisomy 21) caused by an extra
    21st chromosome

12
Chromosomal Disorders
  • Klinefelter syndrome an extra X chromosome in a
    male (XXY)
  • XYY males that are somewhat taller than normal
  • Turner syndrome a missing sex chromosome (XO)
  • cri du chat caused by a deletion in chromosome
    5 (causes mental retardation)
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