Genetics
A short stretch of human DNA in 3D: turn the double helix, unzip it, watch it copy itself and watch a gene being read. The course goes from genes and base pairs to chromosomes, Mendel's peas, Punnett squares, mutations and the tools used to copy, read and edit DNA. It is general information, not medical or genetic-counselling advice.
About this course
Friedrich Miescher first observed DNA in the late 1800s, but for decades most scientists thought it too simple to carry hereditary information and expected proteins to do the job. In 1953 the work of James Watson, Francis Crick, Maurice Wilkins and Rosalind Franklin showed it is a double helix. Franklin's X-ray diffraction images were the key data that Watson and Crick used to build their model. Watson, Crick and Wilkins received the Nobel Prize in 1962; Franklin had died in 1958, and the prize is not awarded after death.
The seven units go from the molecule to the tools. Genes and DNA come first: one human cell holds about 3 billion bases, and only about 1 percent of them spell out proteins. Base pairs follow, where each step of the ladder rises 0.34 nm and ten steps make a 3.4 nm turn. Chromosomes explain how about 2 meters of DNA fit in a cell. Then Mendel: in 1865 he reported crosses of nearly 30,000 pea plants, but almost nobody took notice until other scientists rediscovered his work in 1900. Punnett squares predict that two Yy plants give green seeds one time in four. Mutations show that changing one A to a T in the 20th base of the beta-globin gene gives the variant behind sickle cell disease, and DNA technology notes that 30 rounds of PCR make about a billion copies. The 3D DNA model lets you turn the helix, unzip it and watch it copy. A second lab sets up crosses of Vv × Vv plants.
This is general information, not medical or genetic-counselling advice.
Before you start
Genes live in cells, so Cells is the natural place to begin if the nucleus and chromosomes are new to you. For Mendel's crosses and Punnett squares you only need simple fractions, such as one in four, which Fractions covers.
When you finish
Afterwards you can name the three parts of a nucleotide, pair A with T and C with G, and explain why a codon needs three bases. You can predict the 3 to 1 ratio in Mendel's peas, fill in a Punnett square for a YyRr cross, recognise a point mutation such as the one behind sickle cell disease, and count PCR copies after a number of cycles.
- 1Genes and DNAOne human chromosome set holds about 3 billion DNA base pairs; about 1 percent of its sequence codes for proteins.
- 2Base pairsEach step of the DNA ladder rises 0.34 nm, and ten steps make one full turn of 3.4 nm.
- 3ChromosomesStretched end to end, the DNA in a single human cell would reach about 2 meters.
- 4Mendel's pea plantsIn 1865 a monk in Brno reported crosses of nearly 30,000 pea plants, and the same 3 to 1 ratio kept turning up.
- 5Punnett squaresA 2 by 2 grid predicts that two Yy pea plants give green seeds one time in four.
- 6MutationsChange one A to a T in the 20th base of the beta-globin gene, and the result is the variant behind sickle cell disease.
- 7DNA technologyThirty rounds of PCR turn one piece of DNA into about a billion copies.
Sources for this course (11)
- NHGRI "Deoxyribonucleic Acid (DNA) Fact Sheet" (genome.gov/about-genomics/fact-sheets/Deoxyribonucleic-Acid-Fact-Sheet)
- "Chromosomes Fact Sheet" (genome.gov/about-genomics/fact-sheets/Chromosomes-Fact-Sheet)
- "Human Genome Project" and its timeline (genome.gov/human-genome-project, genome.gov/human-genome-project/timeline)
- "Telomere-to-Telomere" (genome.gov/about-genomics/telomere-to-telomere)
- "Polymerase Chain Reaction (PCR) Fact Sheet" (genome.gov/about-genomics/fact-sheets/Polymerase-Chain-Reaction-Fact-Sheet)
- "What is Genome Editing?" (genome.gov/about-genomics/policy-issues/what-is-Genome-Editing)
- "Human Genomic Variation" (genome.gov/about-genomics/educational-resources/fact-sheets/human-genomic-variation)
- OpenStax Biology 2e , 12.1 "Mendel's Experiments and the Laws of Probability", 12.2 "Characteristics and Traits", 14.2 "DNA Structure and Sequencing", 14.6 "DNA Repair" (openstax.org/books/biology-2e)
- MedlinePlus Genetics "HBB gene" and "Sickle cell disease" (medlineplus.gov/genetics)
- NCBI RefSeq NM_000518.5 (HBB coding sequence) and ClinVar VCV000015333 (c.20A>T, p.Glu7Val)
- Nobel Prize in Chemistry 2020 summary (nobelprize.org/prizes/chemistry/2020/summary)
Checked: 2026-10-17