Why can deleting one base after the start codon change later amino acids?
One DNA base is replaced by another within a protein-coding sequence. Which description identifies the mutation and a possible coding effect?
Proofreading during DNA copying and later mismatch repair can correct copying errors before they persist as mutations.
Circle one: True False
A DNA substitution changes an internal mRNA codon from CAA to UAA, before the usual stop. CAA encodes glutamine; UAA means stop. What happens during translation?
A DNA substitution changes an mRNA codon from CAA to CAG. Both encode glutamine. What happens at this position in the amino acid sequence?
Mutation A changes an active-site amino acid and tests show reduced substrate binding. Mutation B changes an amino acid elsewhere, with unchanged folding and activity in the same tests. Which comparison matches the results?
A DNA substitution replaces one base without changing the base count. The enzyme has one amino acid replacement and its usual chain length, but no longer binds its substrate. Which possible mechanism fits these observations?
A DNA substitution changes one amino acid in a protein, yet the organism's observed trait stays the same. Which explanation fits both observations?