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Published byDamon Sanders Modified over 9 years ago
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What is a mutation? A mutation is any change in genetic material. There are many ways for mutations to occur. Common point mutations are...
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1. Substitution: one base is switched for another
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2. Insertion: an extra base is inserted (put into) the DNA sequence
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3. Deletion: a base is removed from the DNA sequence
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Insertions and deletions are called frame shift mutations because they can cause a shift in the grouping of codons changing an entire amino acid sequence.
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Chromosomal Mutations change the number or structure of chromosomes. Example: Down Syndrome results from an extra chromosome on pair #21
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Genetic Disorders from Mutations Colorblindness Huntington’s disease Cystic Fibrosis Spinabifida Hemophilia Muscular dystrophy Sickle Cell Anemia Turner Syndrome
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Significance of Mutations Mutations can be… 1.harmful. –genetic disorders, deformities, death 2.beneficial. –resistance to disease, better camouflage, stronger muscles; important for evolution! 3.neutral. –No effect
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What causes mutations? 1.Just happen for multiple reasons, many are unknown 1.Mutagens: external (environmental) triggers that cause gene mutations. –Chemicals (like in cigarettes & asbestos) –Radiation (like x-rays, UV light exposure, & gamma radiation from nuclear energy.) –Viruses
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