Predicting Inheritance: Monohybrid Crosses (AQA A Level Biology): Revision Note

Exam code: 7402

Lára Marie McIvor

Written by: Lára Marie McIvor

Reviewed by: Ruth Brindle

Updated on

Monohybrid crosses

  • Monohybrid inheritance involves tracking the inheritance of one gene with two alleles

    • It uses known genotypes, phenotypes, and the process of meiosis to predict offspring outcomes

  • During gamete formation, each allele from a homologous pair has an equal chance of being passed on

    • This means the zygote has an equal probability of inheriting either parental allele

  • Genetic diagrams (especially Punnett squares) are used to present this information clearly

  • Predicted genotypes are based on probability, not certainty

  • Observed ratios in offspring may differ from predictions due to random fertilisation of gametes

Worked Example

  • One of the genes for the coat colour of horses has the following two alleles:

    • B, a dominant allele → produces a black coat when present

    • b, a recessive allele → produces a chestnut coat when present in a homozygous individual

  • In this example, a heterozygous male is crossed with a heterozygous female

Parental phenotype:   black coat x black coat

Parental genotype:     Bb                   Bb

Parental gametes:      B or b              B or b

Punnett square diagram showing coat colour inheritance with male gametes B, b and female gametes B, b. Results: BB, Bb black coat, bb chestnut coat.
Monohybrid punnett square with heterozygous genotypes table
  • Predicted ratio of phenotypes in offspring – 3 black coat : 1 chestnut coat

  • Predicted ratio of genotypes in offspring – 1 BB : 2 Bb : 1 bb

Codominance

  • When working with codominant alleles, the genetic diagrams can be constructed in a similar way, however, the genotypes are represented using a capital letter for the gene and superscript letters for the alleles (eg. IAIA)

  • There will be more possible phenotypes and so the predicted ratios will be different

Worked Example

  • The gene for blood type has three alleles:

    • A, a dominant allele → produces blood type A

    • B, a dominant allele → produces blood type B

    • O, two recessive alleles → produces blood type O

  • In this example, a blood type A person is crossed with a blood type B person

Parental phenotype:   Blood type A x Blood type B

Parental genotype:     IAIO                  IBIO

Parental gametes:      IA or IO             IB or IO

Monohybrid Punnett Square with Codominance Table, downloadable AS & A Level Biology revision notes
Monohybrid Punnett square with codominant genotypes table
  • Predicted ratio of phenotypes in offspring - 1 Blood type AB : 1 Blood type A : 1 Blood type B : 1 Blood type O

  • Predicted ratio of genotypes in offspring: 1 IAIB : 1 IAIO : 1 IBIO : 1 IOIO

Sex-linkage

  • Sex-linked genes are located on the X chromosome (rarely on Y)

  • Males (XY) have one copy of X-linked genes, so are more likely to express recessive traits

  • For example,

    • XᴬY = unaffected

    • XᵃY = affected

  • Females (XX) have two copies, so can be unaffected, carriers, or affected

  • For example,

    • XᴬXᴬ = unaffected

    • XᴬXᵃ = carrier

    • XᵃXᵃ = affected

  • Males cannot be carriers and do not pass X-linked traits to sons, as they only pass on the Y chromosome

Worked Example

  • Haemophilia is a sex-linked disorder caused by a gene on the X chromosome

  • The gene codes for Factor VIII, a protein essential for blood clotting

    • F = dominant allele → produces normal Factor VIII

    • f = recessive allele → results in no Factor VIII, leading to haemophilia

  • Males only need one copy of f (XᶠY) to be affected, as they have only one X chromosome

  • Females must inherit two copies (XᶠXᶠ) to be affected; heterozygous females (XᶠXF) are carriers

  • Two parents with normal clotting (e.g. XFXᶠ mother and XFY father) can produce a child with haemophilia:

Parental phenotypes: carrier female x normal male

Parental genotypes:      XFXf                              XFY

Parental gametes:      XF or Xf                        XF or Y

Genetics Punnett square showing inheritance of haemophilia, with male and female gametes producing different combinations of normal and haemophilia traits.
Monohybrid punnett square with sex-linkage table
  • Predicted ratio of phenotypes in offspring - 1 female with normal blood clotting : 1 carrier female : 1 male with haemophilia : 1 male with normal blood clotting

  • Predicted ratio of genotypes in offspring: 1 XFXF : 1 XFXf : 1 XFY : 1 XfY

Examiner Tips and Tricks

Tips for drawing Punnet squares

  • Always show your working:

    • Include the possible gametes produced by each parent

    • Do not skip straight to the Punnett square

  • State both the genotype and phenotype of offspring

  • For sex-linked inheritance questions:

    • Read carefully to see if the question refers to all children or a specific sex (e.g. only boys or girls)

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Lára Marie McIvor

Author: Lára Marie McIvor

Expertise: Biology, Psychology & Sociology Subject Lead

Lára graduated from Oxford University in Biological Sciences and has now been a science tutor working in the UK for several years. Lára has a particular interest in the area of infectious disease and epidemiology, and enjoys creating original educational materials that develop confidence and facilitate learning.

Ruth Brindle

Reviewer: Ruth Brindle

Expertise: Biology Content Creator

Ruth graduated from Sheffield University with a degree in Biology and went on to teach Science in London whilst also completing an MA in innovation in Education. With 10 years of teaching experience across the 3 key science disciplines, Ruth decided to set up a tutoring business to support students in her local area. Ruth has worked with several exam boards and loves to use her experience to produce educational materials which make the mark schemes accessible to all students.