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Edexcel GCSE Biology (1BI0) ยท Topic 3: Genetics
Mini-Lesson

Genetics

This mini-lesson walks you through Edexcel Topic 3 — Genetics: sexual vs asexual reproduction; meiosis; DNA structure and the genome; the language of genetics (gene, allele, genotype, phenotype, dominant/recessive); monohybrid crosses with Punnett squares and probabilities; sex determination; variation; and the Human Genome Project.

reproduction & meiosis DNA & inheritance crosses & variation how features pass from parents to offspring

Work through each screen, answer the questions (some are wordy, some are probability calculations) and collect ⭐ stars. Press Start when you're ready.

Reproduction

Sexual vs asexual reproduction

  • Sexual reproduction — two parents; gametes (sex cells) join at fertilisation. It mixes genes, so offspring show variation and are genetically different from their parents and each other.
  • Asexual reproduction — one parent; only mitosis. Offspring are genetically identical clones of the parent, with no variation.

Trade-offs: asexual reproduction is fast and needs no mate, and is good in a stable environment. Sexual reproduction is slower but the variation it creates helps a species survive if the environment changes (raw material for natural selection).

Gametes · meiosis

Meiosis makes gametes

Gametes are made by meiosis, which happens only in the reproductive organs. From one diploid cell (46 chromosomes) it produces four genetically different haploid gametes, each with 23 chromosomes.

46 23232323 diploid cell 4 haploid gametes all genetically different
Meiosis: one division to halve the number, giving 4 different haploid gametes.

Mitosis vs meiosis: mitosis = 2 identical diploid cells (growth/repair). Meiosis = 4 different haploid gametes (sexual reproduction). At fertilisation two gametes (23 + 23) restore the diploid 46.

Quick check

Gametes from meiosis

?A cell in a human ovary divides by meiosis. Which correctly describes the cells produced?
Calculate

Your turn — haploid number

1A human body cell has 46 chromosomes. How many chromosomes are in each sperm cell made by meiosis?
chromosomes
Hint: gametes are haploid — they carry half the diploid number, 46 ÷ 2.
DNA & the genome

DNA structure & the genome

Chromosomes are made of DNA, a double helix of two strands. Each strand is a chain of nucleotides; the rungs are pairs of bases that pair by complementary base pairing:

A pairs with T  ·  C pairs with G
AT CG TA double helix of two strands bases pair: A-T and C-G a gene = a section coding for a protein
DNA is a double helix; a gene is a length of DNA that codes for a protein.

Genome: an organism's genome is its entire set of DNA (all its genes). A gene is a short section of DNA that codes for a particular protein.

Inheritance · key terms

The language of genetics

  • Gene — a section of DNA coding for a protein / feature.
  • Allele — a different version of a gene (e.g. B or b).
  • Genotype — the alleles an organism has (e.g. Bb).
  • Phenotype — the characteristics you can observe (e.g. brown eyes).
  • Homozygous — two same alleles (BB or bb).
  • Heterozygous — two different alleles (Bb).
  • Dominant allele — shows in the phenotype even if only one copy is present (written as a capital, B).
  • Recessive allele — only shows when both alleles are recessive (bb; written lower case).

Watch out: genotype is the alleles (letters); phenotype is the visible feature. A heterozygous individual (Bb) shows the dominant phenotype.

Sort it

Genotype word sort

Tap a genotype or term, then tap the box it belongs to.

🔢 Homozygous

🃏 Heterozygous

👁 Phenotype term

Inheritance · monohybrid cross

Monohybrid crosses & Punnett squares

A Punnett square predicts the offspring of a cross. Here two heterozygous parents (Bb × Bb) for a gene where B (brown) is dominant over b (blue):

B b B b BBBb Bbbb Genotypes: 1 BB : 2 Bb : 1 bb Phenotypes: 3 brown : 1 blue P(brown) = 3/4 = 75% P(blue) = 1/4 = 25%
Bb × Bb gives a 3 : 1 ratio of dominant to recessive phenotypes.

Reading ratios as probability: a 3 : 1 ratio means each offspring has a 3/4 (75%) chance of the dominant phenotype and a 1/4 (25%) chance of the recessive one.

Calculate

Your turn — probability of recessive

2Two Bb parents are crossed (B dominant, b recessive). Using the Punnett square, what is the percentage probability that a child has the genotype bb?
%
Hint: only 1 of the 4 boxes is bb, so probability = 1/4.
Calculate

Your turn — probability of dominant

3For the same Bb × Bb cross, what is the percentage probability that a child shows the dominant (brown) phenotype?
%
Hint: 3 of the 4 boxes (BB, Bb, Bb) show brown, so probability = 3/4.
Calculate

Your turn — a different cross

4A plant with genotype Tt (T = tall, dominant) is crossed with a tt plant. What percentage of the offspring are expected to be short (tt)? (Draw the Punnett square if it helps: Tt × tt.)
%
Hint: Tt × tt gives Tt, Tt, tt, tt — half are tt.
Inheritance · sex determination

Sex determination

Of the 23 pairs of human chromosomes, one pair is the sex chromosomes: XX in females and XY in males. All eggs carry an X; sperm carry either an X or a Y.

X Y X X XXXY XXXY 2 XX (female) : 2 XY (male) = 50% female, 50% male
Whether a Y-carrying or X-carrying sperm fertilises the egg gives a 50 : 50 chance of each sex.
Quick check

Boy or girl?

?Using the XX/XY Punnett square, what determines the sex of a child?
Variation

Variation

Differences between organisms of the same species are called variation. It has two sources:

  • Genetic variation — caused by different alleles (from mutation and from the mixing of genes in sexual reproduction). E.g. natural eye colour, blood group.
  • Environmental variation — caused by surroundings and lifestyle. E.g. a scar, or a plant grown in the shade being shorter.
  • Many features (e.g. height) are affected by both genes and environment.

Mutation: a random change to the DNA base sequence. Most have little or no effect, but occasionally a mutation changes the phenotype and provides new variation for natural selection.

Match it

Match the genetics term

Tap a term on the left, then its meaning on the right.

Term
Meaning
The Human Genome Project

The Human Genome Project

The Human Genome Project (HGP) worked out the order of all the bases in the human genome. Understanding the genome has several benefits:

  • Predicting and preventing disease by identifying genes linked to inherited disorders.
  • Developing new and better medicines and testing which drugs suit an individual.
  • Understanding inherited disorders and human ancestry/evolution.

Concerns to evaluate: genetic information could be misused, for example by insurers or employers, and could cause anxiety or discrimination — so data must be handled ethically.

Recap

The big ideas to know

Reproduction: sexual (2 parents, gametes, variation) vs asexual (1 parent, mitosis, clones)

Meiosis: 1 diploid cell → 4 different haploid gametes (23 chromosomes)

DNA: double helix; nucleotides; bases A-T and C-G; genome = all the DNA

Terms: gene, allele, genotype, phenotype, homozygous/heterozygous, dominant/recessive

Crosses: Bb × Bb → 3 : 1 phenotype ratio; ratios give probabilities (75% / 25%)

Sex: XX female, XY male, 50 : 50 · Variation: genetic + environmental · HGP benefits & concerns

You've covered the core of Edexcel Topic 3 — Genetics. Press Finish to see your score.

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Mini-lesson complete!

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