B9 GeneticsRecap & Recall · Y8
First lesson back

Genetics — Recap & Recall

DNA structure · Inheritance · Punnett squares · Sex determination · Genetic disorders
Whiteboards out. We check what’s stuck first, then for each idea you try to recall it before we reveal it, and practise straight away. Finish in your books.
Diagnostic · hinge questions

Whiteboards out — 1, 2, 3 or 4?

Don’t recap yet. Use the spread of answers to decide what to dwell on. Click Reveal for the answer and what each wrong choice tells you.

Section A · DNA structure

The shape of DNA

Drag to rotate the model
DNA is a polymer — a long chain of repeating nucleotides, twisted into a double helix. The two sides are a sugar–phosphate backbone.

Recall first

On your whiteboard, before we reveal

(1) Sketch the shape of DNA. (2) What are the two sides made of? (3) Write the four bases and which one pairs with which.

  • DNA is found in the nucleus, packaged into chromosomes.
  • Its shape is a double helix — a twisted ladder.
  • The two sides (the backbone) are made of sugar and phosphate.
  • The rungs are pairs of bases. There are four: A  T  C  G.
  • The bases pair up: A–T and C–G (complementary base pairing).
  • One repeating unit — sugar + phosphate + base — is a nucleotide.
  • The order (sequence) of the bases is the genetic code.

Quick task · pair the bases

Tap a base, then tap the slot to show its partner. Then press Check.

Independent practice A

Score: 0 / 0
Section B · Genes, alleles, genotype & phenotype

The language of inheritance

Build the schema · chromosome → gene → alleles

Drag to rotate
A homologous pair — one chromosome inherited from each parent. They carry the same genes in the same places.
Left chromosome: B — brown allele
Right chromosome: b — blue allele
Alleles are different versions of the same gene.

Try it · how dominance decides the phenotype

Pick the two alleles a person inherits and watch the eye colour. Brown (B) is dominant.

Allele from parent 1
Allele from parent 2
Genotype: Bb  ·  Phenotype: Brown eyes
Real eye colour is controlled by several genes — we simplify to one gene here to learn how dominance works.

Recall first

On your whiteboard, before we reveal

Define each in your own words: gene · allele · dominant · recessive · genotype · phenotype · homozygous · heterozygous.

  • Gene — a section of DNA that codes for a characteristic.
  • Allele — a different version of a gene.
  • Dominant (F) — shows in the phenotype with just one copy.
  • Recessive (f) — only shows when two copies are present (ff).
  • Genotype — the alleles an organism has (e.g. Ff).
  • Phenotype — the characteristic you actually see.
  • Homozygous — two of the same allele (FF or ff). Heterozygous — two different (Ff).

Quick task · match the term to its meaning

Tap a card, then tap where it goes. Tap a filled space to send it back. Then Check.

Independent practice B

Score: 0 / 0
Section C · Punnett squares

Predicting the offspring

Recall first

On your whiteboard, before we reveal

Write the steps for completing a Punnett square. Then predict: for Ff × Ff, what is the ratio of offspring?

  1. Write both parents’ genotypes.
  2. Find each parent’s gametes (one allele each).
  3. Draw a 2×2 grid — gametes on top and side.
  4. Combine to fill every cell, then count the ratio.
  5. State the probability for each pregnancy.
Worked: Ff × FfFF, Ff, Ff, ff → 3 unaffected : 1 affected → 1 in 4 (25%) each pregnancy.

Quick task · build the Punnett square (Ff × Ff)

The gametes are given. Tap a genotype card, then tap a cell. Then Check.

F
f
F
f

Independent practice C

Score: 0 / 0
Section D · Sex determination

Boy or girl?

Recall first

On your whiteboard, before we reveal

Which sex chromosomes make a female and a male? And who determines the baby’s sex — the mother or the father?

  • Sex chromosomes: XX = female, XY = male.
  • Mother is XX → every egg carries an X.
  • Father is XY → sperm carries an X or a Y.
  • So the father’s sperm determines the sex.
  • XX × XY → 50% XX : 50% XY → roughly 50:50.

Independent practice D

Score: 0 / 0
Section E · Genetic disorders

When alleles cause disorders

Recall first

On your whiteboard, before we reveal

What is a carrier? What is the difference between a dominant and a recessive disorder? What does embryo screening involve?

  • Genetic disorders are caused by faulty alleles passed from parents.
  • Recessive — cystic fibrosis: need two faulty alleles (ff) to be affected.
  • Carrier (Ff): one faulty allele, healthy, can pass it on. Two carriers → 1 in 4 affected.
  • Dominant — polydactyly (extra fingers/toes): one faulty allele is enough.
  • Embryo screening (IVF + PGD): IVF embryos are tested for the faulty allele before one is implanted. Raises ethical questions on both sides.

Independent practice E

Score: 0 / 0
Misconception · address it now

“1 in 4” — what it really means

A pupil says…

“A 1 in 4 chance means one in every four of their children will have cystic fibrosis.”

Actually…

1 in 4 is the probability for each pregnancy, worked out fresh every time — like flipping a coin. Two carriers could have four affected children, or none at all. The dice don’t remember the last roll.

Closer

Say it, then write it

30-second oracy

Explain to your partner: what is the difference between a carrier and an affected person?

Use the words allele · recessive · genotype.

📓 Now open your books and complete the Genetics — Recall & Apply worksheet. Show your Punnett square for Q5 and attempt the Challenge.