A genetic mutation refers to a change in the sequence of nucleotides in DNA. This can occur due to copying errors during cell division, exposure to radiation, certain chemicals, or viruses, or can be inherited from a parent. Mutations can be beneficial, neutral, or harmful to an organism.
A mutation that occurs in the homeotic genes can be particularly impactful, as it disrupts the normal development plan of the organism. These mutations can be categorized into different types:
- Point mutations: a single nucleotide change.
- Insertions and deletions: addition or loss of nucleotides in the DNA sequence.
- Frameshift mutations: insertions or deletions that change the 'reading frame' of the gene.
- Chromosomal mutations: larger changes that affect whole sections of a chromosome or entire chromosomes.
Whether a mutation will manifest as a noticeable trait or have subtle effects depends on its nature and the gene affected. In developmental biology, studying mutations in homeotic genes has been profoundly important for understanding how complex organisms are built from a simple set of instructions.