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Monohybrid Inheritance

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Monohybrid Inheritance Section 11 Monohybrid Inheritance Gregor Mendel (1822-1884): - Used varieties of pea plant - Ensured large numbers were used - Studied only 1 ... – PowerPoint PPT presentation

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Title: Monohybrid Inheritance


1
Monohybrid Inheritance
  • Section 11

2
Monohybrid Inheritance
  • Gregor Mendel (1822-1884)
  • - Used varieties of pea plant
  • - Ensured large numbers were used
  • - Studied only 1 characteristic
  • - Observed 31 phenotypic ratio
  • Principle of segregation the alleles of a gene
    exist in pairs but when gametes are formed, the
    numbers of each pair pass into different gametes.
    Thus each gamete contains only one allele of each
    gene.

3
  • Homozygous (TT) or (tt) 2 of the same allele
  • Heterozygous (Tt) 2 different alleles

4
Law of probability
  • Most monohybrid crosses give roughly 31
    phenotypic ratio
  • 1 in 4 chance of a recessive allele being
    expressed
  • 200 animals roughly 150 have 1 phenotype, 50
    will have another
  • Since fertilisation is random rarely 31 exactly

5
Monohybrid Inheritance in humans
  • Family trees used to predict genetic trends
  • E.g. tongue rolling
  • Rhesus D antigen
  • D-antigen found on some blood cells
  • Present Rhesus positive blood (Rh)
  • Absent Rhesus negative (Rh-)
  • Rh- people produce anti-D antibodies
    sensitised
  • Antigen-D present (DD/Dd)
  • Antigen-D absent (dd)

6
Monohybrid Inheritance in humans
  • Albinism
  • Inability to make melanin pigment for skin,
    eyes, hair etc.
  • Is a recessive trait
  • AA or Aa normal
  • aa albino
  • Other examples
  • - Cystic Fibrosis (mucus secretion)
  • - Phenylketonuria (PKU)
  • - both are recessive traits

7
Monohybrid Inheritance in humans
  • Huntingdons Chorea
  • Determined by a dominant allele
  • Only expressed after average of 38 years old
  • 50 chance of children of Huntingdons sufferer
    getting the disorder
  • 1 in 20,000 cases

8
Incomplete dominance sickle cell anaemia
  • Mutation of haemoglobin gene haemoglobin S
    synthesised
  • Homozygous (SS) Sickle cell anaemia
  • - reduced oxygen carrying capacity
  • - blood cells malformed (sickle-shaped)
  • Heterozygous (HS) Sickle cell trait
  • - both types of haemoglobin present
  • - neither H or S are dominant (incomplete
    dominance)
  • - sickle cell malaria resistance

9
Incomplete / Co-Dominance
  • Incomplete both alleles expressed in the
    phenotype, but unevenly
  • - sickle-cell more H than S expressed
  • Co-Dominance - both alleles equally expressed in
    the phenotype
  • - AB blood exactly 5050 split
  • - MN blood - another blood type antigen
  • - no antibodies produced
  • - equal expression (equal
    dominance

10
Multiple Alleles
  • 3 or more alleles for a characteristic
  • 3 alleles 6 possible genotypes
  • No. of phenotypes depend on the type of dominance
  • complete, incomplete or co-dominance
  • E.g ABO blood 6 genotypes, 4 phenotypes
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