Mutation is a change in the DNA sequence of an organism. It can occur due to various factors such as errors during DNA replication, exposure to mutagenic agents (e.g. radiation, chemicals), or environmental factors.
Types of Mutations
There are several types of mutations:
Point Mutation: A single nucleotide base is replaced with another, which can result in different amino acids being coded for in the protein synthesis process.
Insertion: An extra nucleotide base is added into the DNA sequence.
Deletion: A nucleotide base is removed from the DNA sequence.
Frameshift Mutation: Insertion or deletion of nucleotides causes a shift in the reading frame, leading to a completely different protein being produced.
Chromosomal Mutation: Involves changes in the structure or number of whole chromosomes, such as translocations, inversions, or duplications.
It's also helpful to practice analyzing and interpreting examples of mutations in DNA sequences, and understand the methods used to study and detect mutations.
Ask questions to clarify relationships about the role of DNA and chromosomes in coding the instructions for characteristic traits passed from parents to offspring.
Apply concepts of statistics and probability to explain the variation and distribution of expressed traits in a population.