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Types of Mutations
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Mutations A mutation is a change in the genome (DNA/RNA) strand
Specifically the sequence (order of the DNA nucleotides) Mutations can cause no change in a protein or they can cause the protein to not function
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Mutations Point mutations-
a change in the genetic code that affects only one nucleotide (base) in the DNA sequence Can sometimes lead to a change in the amino acid sequence If a point mutation occurs that doesn’t change the amino acid coded for, it is what is called a silent mutation.
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Mutations A point mutation can lead to nonsense
Nonsense mutation- results in a stop codon in the middle of the amino acid (protein) and therefore it is completely nonfunctional. Stops the production of proteins, so no protein is made
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Mutations A point mutation can lead to missense
Missense mutation- results in a complete protein, but with at least one amino acid different. Results in a different protein that is less functional than before
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There are 3 basic things that can occur in the nucleotide sequence to result in a sense or nonsense mutation: substitutions, Insertions deletions
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A substitution occurs when one base replaces another base.
An insertion is the addition of a base somewhere in the nucleotide sequence. A deletion is the loss of a nucleotide in the DNA sequence.
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Insertion and deletion can cause a frameshift
Frameshift- when the mRNA nucleotides “shift” or move the whole sequence over Insertion and deletion can cause a frameshift A frameshift can create missense mutations or nonsense
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