Mutationby madhuhewa&judygarza
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Transcript of Mutationby madhuhewa&judygarza
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Mutations
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• What is the definition of mutation?-A mutation is a change or any mistake in DNA sequence
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Mutants…
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Types of mutations:
• Point Mutations• Frameshift Mutations• Chromosomal Mutations
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Point mutations:
• Point mutations are single-base changes in a gene’s DNA sequence.
• These include: -Missense mutations -Nonsense mutations -Silent mutations
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Point mutations: Missense mutation
• Missense mutation: Change in a single amino acid within a protein.
• This does change in protein.Example:
Normal: THE DOG BIT THE CAT Mutated: THE DOG BIT THE CAR
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Point Mutations: Nonsense mutation
• Nonsense mutation: Nonsense mutations make a premature stop codon that causing the protein to be shortened.
• Nonsense mutation does change the resulting protein.
Example: Normal: THE DOG BIT THE CAT Mutated: THE DOG BIT
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Point Mutations: Silent mutation
• Silent mutation: Silent mutations change the DNA sequence(not the amino acid sequence).
• Silent mutation does not change the resulting protein and no effect on an organism.
Example: Normal: THE DOG BIT THE CAT Mutated: THE DOG BIT THE KAT
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Frameshift Mutations
• Frameshift Mutations: Frameshift Mutation is insertion or deletion of one or more bases into or from the DNA sequence.
• This effect on every amino acid in the protein and it makes protein nonfunctional.
Example:
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Frameshift Mutation:
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Chromosomal Mutations:
4 types of chromosomal Mutations:• Translocation: A chromosomal segment is
transferred to a new position on the same or another chromosome
• Deletion: the loss or absence of one or more nucleotides from a chromosome
• Inversion: Part of a chromosome breaks out and is reinserted backwards
• Insertion: Part of the chromosome is broken off and attaches to the sister chromatid.
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Chromosomal Mutations:
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Causes of Genetic Mutations:
• Sometimes it happens for no reason (Spontaneous Mutations).
• Environmental Causes: -UV light - Radiation - X-rays -Some Chemicals
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Genetic Disorders:
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Cystic Fibrosis
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Osteogenesis Imperfecta
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Multiple Neurofibromastosis
• genetically-inherited disorder• Multiple begins tumors that form in
skin
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Klinefelter’s Syndrome• Males have XXY sex chromosomes:
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Twin-to-Twin Transfusion Syndrome
• Due to placental abnormality, one twin receives too much blood and the other does not receive enough.
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Fragile X Syndrome