DNA and Genetics
  The Basics
    7th Science
    Mr. Bombick
Major DNA Subunit
• Nucleotide contains a base, a
  sugar, and a phosphate
• The four bases in DNA are
  Adenine (A), Thymine (T),
  Guanine (G), and Cytosine (C)
DNA Structure
• Each strand of the double stranded
  DNA is comprised of nucleotides
  connected by the phosphates
• The double strand of DNA is held
  together by hydrogen bonding between
  complementary bases
• A (adenine) is paired with T (thymine)
• G (guanine) is paired with C (cytosine)
DNA organization in the cell
    • One double strand of DNA is
      compacted within the nucleus by
      coiling around specific proteins to
      produce chromatin
    • Chromatin is further compacted
      into chromosomes
Information contained in DNA
       • DNA contains many genes
       • Genes are sections of DNA that
         contain the code for proteins
       • One gene is responsible for one
         protein
       • Proteins are responsible for the
         different genetic traits in
         individuals
DNA Mutations
• A mutation is a change in a
  specific region of a gene
• The mutation results in an
  alteration in the type of protein
  (or whether a protein is made at
  all) coded by the gene
• Mutations can be caused by a
  variety of environmental or
  physiological factors
DNA Replication
• DNA is replicated just prior to when a
  non-sex cell undergoes cell division
• The double-stranded DNA is split down
  the middle of the bases for a short
  length of the DNA
• Nucleotides are inserted (with the
  appropriate base pairing) into the
  exposed single strand
• Completion of replication results in two
  identical double-stranded DNA
  molecules
Human Chromosome Organization
     • Humans have 23 pairs of chromosomes (46
       chromosomes)
     • During non-germ cell division (mitosis) the
       23 pairs of chromosomes are copied
       resulting in each of the two new cells
       having 23 pairs of chromosomes
     • During germ cell division (meiosis) each
       germ (sperm or egg) ends up with only 23
       chromosomes
     • (use board to illustrate an example of
       differences resulting from mitosis and
       meiosis)
Importance of Meiosis in Genetics
      • Meiosis results in each germ cell (egg
        or sperm) having half of the
        chromosomes of the normal cell (for
        humans this would be 23 chromosomes)
      • Fertilization (combination of egg and
        sperm) will result in the normal number
        of chromosomes in the cell (for humans
        this would be 46 chromosomes)
      • Therefore, half of the chromosomes
        will come from the male and half of the
        chromosomes will come from the
        female
Basis of Genetics
• Probability
• Nature of the trait (gene or
  allele)
• Behavior of chromosomes in
  the process of meiosis
Movement of Chromosomes in Meiosis
       • Meiosis is a process by which the
         chromosome number is reduced by
         one-half of the typical number of
         chromosomes in a cell
       • Therefore, each germ cell (egg or
         sperm) contains one-half of the
         number of chromosomes
       • Fertilization will result in the
         normal number of chromosomes
         (for humans this equals 46)
Segregation of Alleles
  • An allele is a form of a gene (a region of
    the chromosome that “codes” for a
    specific protein)
  • In a simple situation, two types of
    alleles might consist of dominant or
    recessive alleles
  • In meiosis the two alleles of the male or
    female end up segregated so only one
    allele is contained in the germ cell (egg
    or sperm)
Types of Alleles
• Simplest case is where alleles are
  dominant or recessive
• Alleles also may be co-dominant
  where both alleles are expressed
  in the offspring (blood type is a
  typical example)
• Alleles also may exhibit incomplete
  dominance (an example will follow
  later in this presentation)
• Alleles may also be sex-linked
  where the alleles are on the sex
  chromosomes
Important Genetic Terminology
   • Dominant Allele—results in the expression of
     this trait in the offspring
   • Recessive Allele—trait is only expressed in
     offspring if there are two recessive alleles
   • Heterozygous—presence of one dominant and
     one recessive allele
   • Homozygous—presence of two dominant or
     two recessive alleles
   • Phenotype—the resulting expression of the
     two alleles in the offspring
   • Genotype—the actual genetic composition of
     the two alleles in the offspring
Punnett Square
• Graphical way of predicting possible
  genetic outcomes (both genotypes and
  phenotypes) in offspring from parents
• In a Punnett square the alleles from
  each parent are shown on the top and
  left side of the square
• The possible genotypes are then
  calculated in the individual boxes in the
  Punnett square
• Allows the calculation of ratios of
  genotypes and phenotypes of the
  offspring
Examples of Punnett Squares
    (on the blackboard)
     •   Example of a single trait cross
     •   Example of a cross with two traits
     •   Example of a sex-linked cross
     •   Example of co-dominant cross
     •   Example of incomplete dominant
         cross
The End

Dna and genetics_basic_power_point__1-14-11[1]

  • 1.
    DNA and Genetics The Basics 7th Science Mr. Bombick
  • 2.
    Major DNA Subunit •Nucleotide contains a base, a sugar, and a phosphate • The four bases in DNA are Adenine (A), Thymine (T), Guanine (G), and Cytosine (C)
  • 3.
    DNA Structure • Eachstrand of the double stranded DNA is comprised of nucleotides connected by the phosphates • The double strand of DNA is held together by hydrogen bonding between complementary bases • A (adenine) is paired with T (thymine) • G (guanine) is paired with C (cytosine)
  • 4.
    DNA organization inthe cell • One double strand of DNA is compacted within the nucleus by coiling around specific proteins to produce chromatin • Chromatin is further compacted into chromosomes
  • 5.
    Information contained inDNA • DNA contains many genes • Genes are sections of DNA that contain the code for proteins • One gene is responsible for one protein • Proteins are responsible for the different genetic traits in individuals
  • 6.
    DNA Mutations • Amutation is a change in a specific region of a gene • The mutation results in an alteration in the type of protein (or whether a protein is made at all) coded by the gene • Mutations can be caused by a variety of environmental or physiological factors
  • 7.
    DNA Replication • DNAis replicated just prior to when a non-sex cell undergoes cell division • The double-stranded DNA is split down the middle of the bases for a short length of the DNA • Nucleotides are inserted (with the appropriate base pairing) into the exposed single strand • Completion of replication results in two identical double-stranded DNA molecules
  • 8.
    Human Chromosome Organization • Humans have 23 pairs of chromosomes (46 chromosomes) • During non-germ cell division (mitosis) the 23 pairs of chromosomes are copied resulting in each of the two new cells having 23 pairs of chromosomes • During germ cell division (meiosis) each germ (sperm or egg) ends up with only 23 chromosomes • (use board to illustrate an example of differences resulting from mitosis and meiosis)
  • 9.
    Importance of Meiosisin Genetics • Meiosis results in each germ cell (egg or sperm) having half of the chromosomes of the normal cell (for humans this would be 23 chromosomes) • Fertilization (combination of egg and sperm) will result in the normal number of chromosomes in the cell (for humans this would be 46 chromosomes) • Therefore, half of the chromosomes will come from the male and half of the chromosomes will come from the female
  • 10.
    Basis of Genetics •Probability • Nature of the trait (gene or allele) • Behavior of chromosomes in the process of meiosis
  • 11.
    Movement of Chromosomesin Meiosis • Meiosis is a process by which the chromosome number is reduced by one-half of the typical number of chromosomes in a cell • Therefore, each germ cell (egg or sperm) contains one-half of the number of chromosomes • Fertilization will result in the normal number of chromosomes (for humans this equals 46)
  • 12.
    Segregation of Alleles • An allele is a form of a gene (a region of the chromosome that “codes” for a specific protein) • In a simple situation, two types of alleles might consist of dominant or recessive alleles • In meiosis the two alleles of the male or female end up segregated so only one allele is contained in the germ cell (egg or sperm)
  • 13.
    Types of Alleles •Simplest case is where alleles are dominant or recessive • Alleles also may be co-dominant where both alleles are expressed in the offspring (blood type is a typical example) • Alleles also may exhibit incomplete dominance (an example will follow later in this presentation) • Alleles may also be sex-linked where the alleles are on the sex chromosomes
  • 14.
    Important Genetic Terminology • Dominant Allele—results in the expression of this trait in the offspring • Recessive Allele—trait is only expressed in offspring if there are two recessive alleles • Heterozygous—presence of one dominant and one recessive allele • Homozygous—presence of two dominant or two recessive alleles • Phenotype—the resulting expression of the two alleles in the offspring • Genotype—the actual genetic composition of the two alleles in the offspring
  • 15.
    Punnett Square • Graphicalway of predicting possible genetic outcomes (both genotypes and phenotypes) in offspring from parents • In a Punnett square the alleles from each parent are shown on the top and left side of the square • The possible genotypes are then calculated in the individual boxes in the Punnett square • Allows the calculation of ratios of genotypes and phenotypes of the offspring
  • 16.
    Examples of PunnettSquares (on the blackboard) • Example of a single trait cross • Example of a cross with two traits • Example of a sex-linked cross • Example of co-dominant cross • Example of incomplete dominant cross
  • 17.