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Chapter 12: DNA and RNA (12-4) Sometimes mistakes are made—these mistakes are called mutations (latin for mutare, “to change”) Mutations are changes in the DNA sequence that affect genetic information Gene mutations result from changes in a single gene. Chromosomal mutations involve changes in whole or part of chromosomes. Point mutations Affect only ONE nucleotide One amino acid in the chain is wrong Substitution of a nitrogen base (A instead of G, etc) Framshift Mutations Involve a deletion or substitution of a nitrogen base Causes a much bigger problem, because the code is read in 3s This shifts the “reading frame” of the genetic message. Every amino acid is affected after the mutation. Severely affect the function/shape of the protein. Chapter 12: DNA and RNA (12-4) Change in the number or structure of chromosomes Deletion—loss of part or all of the chromosome Duplication—segment of the chromosome is repeated Inversion—the chromosome is oriented in reverse Translocation—when part of one chromosome breaks off and attaches to another non-homologous chromosome.