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Biology AS CIE

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  1. 1-cell-structure
    10 主题
  2. 2-biological-molecules
    19 主题
  3. 3-enzymes
    13 主题
  4. 4-cell-membranes-and-transport
    16 主题
  5. 5-the-mitotic-cell-cycle
    8 主题
  6. 6-nucleic-acids-and-protein-synthesis
    9 主题
  7. 7-transport-in-plants
    11 主题
  8. 8-transport-in-mammals
    16 主题
  9. 9-gas-exchange
    6 主题
  10. 10-infectious-diseases
    6 主题
  11. 11-immunity
    10 主题
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Exam code:9700

Gene mutations & their effect on polypeptides

  • A gene mutation is a change in the sequence of base pairs in a DNA molecule that may result in an altered polypeptide

  • As the DNA base sequence determines the sequence of amino acids that make up a protein, mutations in a gene can sometimes lead to a change in the polypeptide that the gene codes for

  • Most mutations do not alter the polypeptide or only alter it slightly so that its structure or function is not changed

    • This is because the genetic code is degenerate

  • There are different ways that a mutation in the DNA base sequence can occur:

Insertion of nucleotides

  • A mutation that occurs when a nucleotide (with a new base) is randomly inserted into the DNA sequence is known as an insertion mutation

  • An insertion mutation changes the amino acid that would have been coded for by the original base triplet, as it creates a new, different triplet of bases

  • An insertion mutation also has a knock-on effect by changing the triplets (groups of three bases) further on in the DNA sequence

    • This is sometimes known as a frameshift mutation

  • This may dramatically change the amino acid sequence produced from this gene and therefore the ability of the polypeptide to function

Diagram showing mutation effects on genes. Original sequence: tyrosine, serine, leucine. Mutated gene with inserted base: tyrosine, arginine, serine.
An example of an insertion mutation

Deletion of nucleotides

  • A mutation that occurs when a nucleotide (and therefore its base) is randomly deleted from the DNA sequence

  • Like an insertion mutation, a deletion mutation:

    • Changes the amino acid that would have been coded for

    • Has a knock-on effect by changing the groups of three bases further on in the DNA sequence

      • This is another type of frameshift mutation

  • This may dramatically change the amino acid sequence produced from this gene and therefore the ability of the polypeptide to function

Substitution of nucleotides 

  • A mutation that occurs when a base in the DNA sequence is randomly swapped for a different base

  • Unlike an insertion or deletion mutation, a substitution mutation will only change the amino acid for the triplet (a group of three bases) in which the mutation occurs

    • It will not have a knock-on effect (it is not a frameshift mutation)

Diagram showing gene mutation with original sequence coding for tyrosine, serine, leucine, and mutated sequence coding for tyrosine, arginine, leucine.
An example of a substitution mutation

 The effect of gene mutations on polypeptides 

  • Most mutations do not alter the polypeptide or only alter it slightly so that its appearance or function is not changed

  • However, a small number of mutations code for a significantly altered polypeptide with a different shape

  • This may affect the ability of the protein to perform its function

    • For example:

      • If the shape of the active site on an enzyme changes, the substrate may no longer be able to bind to the active site

      • A structural protein (like collagen) may lose its strength if its shape changes

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