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MUTATIONS Changes in DNA can cause changes in phenotype. Changes in the DNA sequence of nucleotides is called a mutation. Some mutations have little or no effect on an organism, others are harmful or fatal, a few can even be beneficial. There are two types of mutation: 1. Chromosomal involves the entire chromosome. 2. Gene - involves individual genes on a chromosome. 4 types of chrom. mutations: Deletion - chromosome breaks apart, and a piece is lost. Duplication - chromosome breaks apart, and the piece incorporates into the homologous chromosome. Translocation - chromosome breaks apart, and the piece incorporates into a non-homologous chromosome. Inversion - chromosome breaks and reattaches in reverse order. There are 3 types of gene mutations: Frameshift - deletion or insertion of nucleotides that disrupts codons. Point or Substitution - change that occurs in only one nucleotide. Cancer is uncontrolled, abnormal cell division Caused when genes that control production of new cells do not shut off. A gene that causes a cell to become cancerous is called an oncogene. Three ways a gene can become an oncogene: Mutation of a growth factor gene An error in DNA replication A change in a gene’s location