Mendelian genetics

Introductory Biology. Also known as: biol 101, biol 1101, biol 1406, bio 101, bio 1010, biol 111, general biology i, biology for majors i, principles of biology, biology 1

Alleles, dominance, Punnett squares and probability, plus incomplete dominance and sex linkage.

Key terms

  • Gene: a unit of heredity. Allele: a version of a gene.
  • Genotype: the allele combination (for example Aa). Phenotype: the observable trait.
  • Homozygous: two identical alleles (AA or aa). Heterozygous: two different alleles (Aa).
  • Dominant alleles (capital letter) show in the phenotype when present. Recessive alleles (lowercase) show only when two copies are present.

Mendel's laws

Gregor Mendel experimented with pea plants and found:

  1. Law of segregation: the two alleles for a gene separate when gametes form, so each gamete carries one.
  2. Law of independent assortment: alleles of different genes sort independently (true for genes on different chromosomes).

Punnett squares

A Punnett square shows possible offspring from the gametes of each parent.

Worked example

In peas, tall (T) is dominant to short (t). Cross two heterozygous plants (Tt × Tt).

  1. Each parent produces gametes T and t in equal numbers.
  2. The square gives: TT, Tt, Tt, tt.
  3. Genotype ratio: 1 TT : 2 Tt : 1 tt.
  4. Phenotype ratio: 3 tall : 1 short, so 25 percent are short.

Now cross Tt × tt (a test cross): the offspring are 1/2 Tt and 1/2 tt, so half are tall and half short. A test cross uses a homozygous recessive partner to reveal the genotype of an organism with the dominant phenotype. If any short offspring appear, the tall parent must be Tt.

Using probability

Independent events multiply. If Tt × Tt, the chance of two children (or plants) both being short is 1/4 × 1/4 = 1/16. The chance that a given offspring is short is always 1/4, whatever happened to earlier ones; chance has no memory.

Beyond simple dominance

  • Incomplete dominance: the heterozygote is intermediate. Crossing red and white snapdragons can give pink.
  • Codominance: both alleles show fully, as in the AB blood type.
  • Polygenic traits: many genes contribute, as with human height and skin colour.

Sex linkage

The X chromosome carries many genes the Y does not. Males (XY) have only one X, so a single recessive allele on it shows. This is why X-linked recessive conditions such as red-green colour blindness are more common in males. A son inherits his X from his mother, never from his father.

Common mistakes

  • Treating "dominant" as "most common". Dominance describes expression, not frequency.
  • Mixing up genotype and phenotype.
  • Forgetting that each child's probability is independent.

Practice questions

  1. Two heterozygous parents (Aa × Aa) have a child. What is the chance of the recessive phenotype?

  2. The genotype of an organism is its…

  3. An organism with two identical alleles for a gene is…

  4. In a cross of Aa × aa, what fraction of offspring show the recessive phenotype?

  5. A test cross is used to…

  6. Crossing red and white snapdragons gives pink offspring. This is…

Full reading: Biology 2e (OpenStax), licence Creative Commons Attribution-NonCommercial-ShareAlike (CC BY-NC-SA). Explanations and questions on this page were written by CoLabEx; no text is copied from the book.

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Mendelian genetics explained: Introductory Biology study guide | CoLabEx