🎯 What you'll practice: The central dogma, transcription/translation mechanics, mutation types, and the sickle cell case study.
1-B 2-B 3-C 4-B | 5 = uracil 6 = tRNA 7 = UAA, UAG, UGA 8 = GAG→GTG substitution changes glutamic acid to valine in beta-globin 9 = A point mutation changes only one base and affects at most one amino acid; a frameshift mutation inserts or deletes a base, shifting the reading frame so every codon after it is misread | 10 = Heterozygous carriers (one sickle allele, one normal allele) make enough normal haemoglobin to avoid severe sickling symptoms, but the sickled cells they do have make it harder for the malaria parasite to complete its life cycle inside red blood cells — so carriers survive malaria better than either homozygous genotype, keeping the allele common despite being dangerous when inherited from both parents.