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4BI1

Genetics & Inheritance

Reproduction and Inheritance · 6 question types

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4BI1 Topics

Reproduction11%
Genetics & Inheritance17%
  1. Key Genetic Terms
  2. DNA Structure
  3. RNA Structure
  4. Protein Synthesis: from Gene to Protein
  5. Monohybrid Inheritance and Punnett Squares
  6. Codominance: When Both Alleles Show
  7. Sex Chromosomes and Sex Determination
  8. Family Pedigrees
  9. Mutations
  10. Sex-linked Inheritance
  11. Sources of Variation: Mitosis vs Meiosis, and Random Fertilisation
  12. Genetic vs Environmental Variation
Natural Selection & Evolution14%

Frequency legend

High (≥14%)
Above avg (10 to 13%)
Average (<10%)

Exam Frequency Analysis

Past paper frequency (2018 to 2024)

This topic accounts for approximately 17% of your exam marks.

increasing
Very High
Increasing17%

Genetic crosses, Punnett squares, and dominant/recessive allele questions appear on almost every paper.

Inheritance is a topic where the right words matter. Most exam questions on genetics rely on you knowing what a gene, an allele, a genotype and a phenotype are, and being able to use these terms precisely.

The big eight

TermWhat it means
DNAThe chemical that carries all the genetic information of an organism. Stands for deoxyribonucleic acid
ChromosomeA long, tightly-coiled molecule of DNA found in the nucleus. Humans have 23 pairs in every body cell
GeneA short section of DNA on a chromosome. Each gene codes for one specific protein
AlleleOne of the different versions of the same gene. A gene might have two or more alleles
GenotypeThe combination of alleles an individual has for a particular gene (e.g. BB, Bb, bb)
PhenotypeThe observable characteristic that results from a particular genotype (e.g. brown eyes, blood group A)
DominantAn allele whose effect is seen in the phenotype even when only one copy is present. Written as a capital letter (e.g. B)
RecessiveAn allele whose effect is only seen in the phenotype when both copies are present. Written as a lowercase letter (e.g. b)

Homozygous and heterozygous

The two alleles you carry for a given gene can be the same or different:

  • Homozygous: both alleles are the same (e.g. BB or bb)
  • Heterozygous: the two alleles are different (e.g. Bb)

If you are heterozygous and one allele is dominant, the dominant version is the one you show in your phenotype. The recessive allele is still there in your genotype, but it is masked by the dominant one.

An example: the PTC tasting gene. Some people can taste a bitter chemical called phenylthiocarbamide (PTC, found naturally in some vegetables like sprouts); others can't taste it at all. The ability to taste PTC is controlled by one gene with two alleles:

  • T = can taste PTC (dominant)
  • t = cannot taste PTC (recessive)
GenotypePossible allelesPhenotype
TTT from each parentTaster (homozygous dominant)
TtT from one parent, t from the otherTaster (heterozygous; T masks t)
ttt from each parentNon-taster (homozygous recessive)

Note that two different genotypes (TT and Tt) produce the same phenotype (taster). The only way to be a non-taster is to have two copies of the recessive allele.

Other terms you should know

  • Genome: the whole of an organism's DNA, taken together. Every chromosome, every gene, every base. Sequencing the entire human genome was completed in 2003.
  • Diploid: a cell with two complete sets of chromosomes (e.g. a human body cell with 23 pairs = 46 chromosomes). Written as 2n.
  • Haploid: a cell with one complete set of chromosomes (e.g. a human sperm or egg with 23 chromosomes). Written as n.
  • Variation: differences between individuals of the same species. Variation can be genetic (caused by different alleles), environmental (caused by lifestyle, diet, accidents), or a mix of both.

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DNA Structure