Codominance & Sex-Linked Characteristics (Cambridge (CIE) IGCSE Biology): Revision Note

Codominance: Extended

Extended Tier Only

Codominance

• Codominance occurs when both alleles in heterozygous organisms contribute to the phenotype

• Inheritance of blood group is an example of codominance

• There are three alleles of the gene governing the inheritance of blood group:

  • Alleles I^A and I^B are codominant

  • Both I^A and I^B are dominant to I^O

• I represents the gene and the superscript A, B and O represent the alleles

• I^A results in the production of antigen A in the blood

• I^B results in the production of antigen B in the blood

• I^O results in no antigens being produced in the blood

• As only two alleles can be inherited by an individual (one from the mother, one from the father), the three alleles can combine to produce the following genotypes and phenotypes:

• Genetic diagrams can be used to predict the outcome of crosses that involve codominant alleles:

• For example: ‘Show how a parent with blood group A and a parent with blood group B can produce offspring with blood group O’

• The parent with blood group A must have the genotype I^AI^O

• The parent with the blood group B must have the genotype I^BI^O

• These are the only possible genotypes (as opposed to both being homozygous) as they are able to produce a child with blood group O and so the child must have inherited an allele for group O from each parent

• Parents with these blood types have a 25% chance of producing a child with blood type O

Sex-linked characteristics: Extended

Extended Tier Only

• Alleles on the same chromosome are said to be linked

• When alleles that control a particular characteristic are found on the sex chromosomes, we describe the inheritance that results as ‘sex linked’

• In almost all cases, there are only alleles on the X chromosome as the Y chromosome is much smaller

• Because males only have one X chromosome, they are much more likely to show sex-linked recessive conditions (such as red-green colour blindness and haemophilia)

• Females, having two copies of the X chromosome, are likely to inherit one dominant allele that masks the effect of the recessive allele

• A female with one recessive allele masked in this way is known as a carrier; she doesn’t have the disease, but she has a 50% chance of passing it on to her offspring

• If that offspring is a male, he will have the disease

• The results of a cross between a normal male and a female who is a carrier for colour blindness is as follows:

• In the cross above, there is a 25% chance of producing a male who is colour blind, a 25% chance of producing a female carrier, a 25% chance of producing a normal female and a 25% chance of producing a normal male