Genetics
- Monohybrid cross (Aa × Aa)
- genotypes 1 : 2 : 1, phenotypes 3 : 1
- Dihybrid cross
- phenotypes 9 : 3 : 3 : 1
- Hardy–Weinberg
- p + q = 1, p² + 2pq + q² = 1
- Independent genes
- multiply the probabilities
Formula sheets, the key method steps for every topic and 4 practice problems, with full solutions at the back.
Tall (A) is dominant over short (a), and round seeds (B) over wrinkled (b). The genes are on different chromosomes. For the cross AaBb × aabb, what is the probability P that an offspring is short, wrinkled seeds?
A recessive condition affects 9% of a population in Hardy–Weinberg equilibrium. What fraction f of the population are carriers (heterozygous)?
What directly drives ATP synthase to make ATP in mitochondria?
In the most common cystic fibrosis mutation (ΔF508), the CFTR protein is made but is missing from the cell membrane. Why?
Answer: P = 0.25
Mendelian genetics: each parent passes on one allele of each gene, chosen at random. A Punnett square lists every combination of gametes, each equally likely. A dominant allele (capital letter) shows whenever it is present; a recessive one only in the homozygous form. Genes on different chromosomes are inherited independently, so their probabilities multiply.
Answer: f = 0.42
Hardy–Weinberg: in a large, randomly mating population with no selection, the allele frequencies p (dominant) and q (recessive), p + q = 1, give genotype frequencies p², 2pq and q².
Answer: A · Protons flowing back into the matrix down their gradient
The electron transport chain pumps protons into the intermembrane space. Their flow back through ATP synthase turns it and powers ATP synthesis.
Answer: D · The misfolded protein is held in the ER and degraded
Loss of one phenylalanine makes CFTR misfold. ER quality control retains it and sends it for proteasomal degradation, so little reaches the membrane.
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