AP BIOLOGY

Detailed explanation-1: -An insertion changes the DNA sequence by adding one or more nucleotides to the gene. As a result, the protein made from the gene may not function properly. A deletion changes the DNA sequence by removing at least one nucleotide in a gene.

Detailed explanation-2: -An insertion mutation occurs when an extra nucleotide is added to the DNA strand during replication. This can happen when the replicating strand “slips, ” or wrinkles, which allows the extra nucleotide to be incorporated (Figure 2). Strand slippage can also lead to deletion mutations.

Detailed explanation-3: -An insertion mutation, also known as a gene insertion or DNA insertion, is a type of mutation where additional nucleotides are inserted into the DNA. DNA is the genetic material of the cell. It contains all of the instructions for cell structure and function.

Detailed explanation-4: -Insertion/Deletion Mutations When a nucleotide is wrongly inserted or deleted from a codon, the affects can be drastic. Called a frameshift mutation, an insertion or deletion can affect every codon in a particular genetic sequence by throwing the entire three by three codon structure out of whack.

Detailed explanation-5: -Frameshift Mutation A frameshift mutation in a gene refers to the insertion or deletion of nucleotide bases in numbers that are not multiples of three. This is important because a cell reads a gene’s code in groups of three bases when making a protein.