Skip to content
Dabour HubLEARN · PRACTICE · EXPLORESign inStudent

3.2.2Genetics

Predicting Genetic Inheritance

5 min read 9 parts Lesson 5 of 9 2 quizzes

0%read

Section 1 of 9Monohybrid crosses

Monohybrid test cross Tt x tt
Monohybrid Cross Simulation - Tall (T) vs Short (t)
monohybrid cross landscape
Monohybrid Cross: Tall (T) vs Short (t) Plants

A monohybrid cross follows the inheritance of one gene with two alleles. A genetic diagram shows the parents, the gametes they produce, and the possible offspring. Follow these steps every time:

1
Define the alleles, giving a letter and stating which is dominant (for example T = tall, t = short).
2
Write the parental genotypes.
3
Write the gametes. Each gamete has one allele, because the pair separates in meiosis.
4
Draw a Punnett square with one parent's gametes along the top and the other's down the side.
5
Fill in the offspring genotypes, then give the phenotypes and the ratio.

Section 2 of 9Example: heterozygous parents

asexual reproduction
Homologous chromosome pairs: homozygous and heterozygous

Cross two heterozygous plants, Tt x Tt. The gametes from each parent are T or t.

Tt
TTTTt
tTttt

The genotypes occur in the ratio 1 TT : 2 Tt : 1 tt.

3 : 1 ratio
The phenotypes are three tall to one short, a 3 : 1 ratio.
The probability of any offspring being short is 1 in 4 (25%).
Each fertilisation is independent, so even if the first three children are tall, the chance of the next being short is still 25%.

Section 3 of 9Other crosses

Homozygous dominant x homozygous recessive (TT x tt) gives all Tt, all tall (F1). Heterozygous x homozygous recessive (Tt x tt) gives 1 Tt : 1 tt, a 1 : 1 ratio of tall to short; this is the test cross. Homozygous dominant x anything gives all offspring showing the dominant phenotype.

Ratios are predictions based on probability. Small families rarely show exact ratios, but in large numbers of offspring the observed results come closer to the predicted ones, the same reason that Mendel counted so many plants.

Section 4 of 9Family pedigrees

Pedigree chart (affected/unaffected males and females)
Family pedigree chart with affected and unaffected members

A family tree (pedigree) can show how an inherited condition passes through a family.

Family pedigrees
Squares are usually males and circles females; shaded shapes show affected people.
Recessive
If two unaffected parents have an affected child, the condition must be caused by a recessive allele and both parents must be carriers (Cc).
The chance that the next child of two carriers is affected is 1 in 4, and 1 in 2 that the child is an unaffected carrier.
If an affected child has only one affected parent in each generation, a dominant allele might be involved.

Cystic fibrosis is a standard example. A person with the condition has the genotype ff; their parents are both Ff. Cystic fibrosis affects roughly 1 in 2500 births in the UK and 1 in 25 people carry the allele.

Section 5 of 9Probability and decisions

Genetic diagrams give probabilities, not certainties.

Probability and decisions
A 25% risk means each pregnancy has a 1 in 4 chance, not that exactly one in four children will be affected.
Couples at risk of passing on a serious condition can get genetic counselling and may choose testing or screening of embryos.
When describing a result, express it as a ratio (3:1), fraction (3/4), percentage (75%) or probability (0.75), as the question asks.

Keep a clear layout, show the gametes in circles if your teacher uses them, and always state the phenotype in words. Markers look for the key, parent genotypes, gametes, offspring genotypes and final ratio, so missing one can lose a mark even when the square is correct.

Section 6 of 9Using ratios and sample sizes

Surface Area : Volume — 3D Step-by-Step Simulation

To turn a predicted ratio into numbers, divide the total by the sum of the parts.

1
For a 3:1 ratio from 200 offspring there are four parts, so each part is 50, giving 150 of the dominant phenotype and 50 of the recessive.
2
Real results rarely match exactly.
3
If a breeder obtains 140 tall and 60 short plants, the result is close to the prediction,
  • and the difference is explained by chance in which gametes meet at fertilisation.
4
A very different result, such as 100:100, would suggest the cross was not as predicted, perhaps because the tall parent was not heterozygous,
  • which the breeder could test.

You may meet a question where a result is given as a ratio of genotypes, as a ratio of phenotypes, or as a probability. Check the question carefully, and always show the working: the key, parent genotypes, gametes, Punnett square, offspring genotypes and the final statement in words.

Section 7 of 9Exam-style questions

Cystic fibrosis inheritance: carrier parents Punnett square
Punnett Square - Cystic Fibrosis Inheritance (Ff x Ff)
Punnett Square — Continuous Flow Simulation
DNA sequence comparison between species
DNA sequence comparison between species
Pedigree showing nonnuclear maternal inheritance
Punnett square and offspring ratio 3 tall : 1 short
Test Cross: Unknown Tall Plant × tt
  1. In cats, the allele for black fur (B) is dominant to the allele for ginger fur (b). Two heterozygous black cats are mated. Draw a genetic diagram to show the possible offspring and state the probability that a kitten is ginger. [5]5 marks

  2. Two parents without cystic fibrosis have a child with the condition. Explain how this is possible. [3]3 marks

  3. A heterozygous tall plant is crossed with a short plant. In total 60 offspring are produced. Predict the number of short plants. [2]2 marks

Section 8 of 9Key terms

TermMeaning
Monohybrid crossA genetic cross that looks at the inheritance of one gene.
Punnett squareA grid showing all possible combinations of gametes in a cross.
Genetic diagramA diagram showing parents, gametes and offspring of a cross.
RatioA comparison of the numbers of each phenotype, such as 3:1.
ProbabilityThe chance of an outcome happening.
PedigreeA family tree showing the inheritance of a feature.
CarrierA person with one copy of a recessive allele who does not show the condition.
Test crossA cross with a homozygous recessive to find an unknown genotype.

Section 9 of 9Exam technique

1
Putting two alleles in a single gamete; each gamete has one.
2
Forgetting a key to show which letter is dominant.
3
Believing that if one child in a family has a recessive condition, the next three will be unaffected.
4
Giving only genotypes and forgetting to state the phenotype ratio.
5
Using different letters for the two alleles.
\n