Summary: Studyguide For Igenetics A Molecular Approach By Peter J. Russell, Isbn 9780805346657 | 9781616984571 | Cram101 Textbook Reviews

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Read the summary and the most important questions on Studyguide for Igenetics A Molecular Approach by Peter J. Russell, ISBN 9780805346657 | 9781616984571 | Cram101 Textbook Reviews

  • 7 DNA mutation, DNA repair and transposable elements

  • 7.1.2 Mutations defined

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  • What is the difference between a "somatic mutation"  and a "germ-line mutation" ? (2)

    • Somatic mutation: affects only the individual itself
    • Germ-line mutation: may be passed on, and create mutations in both somatic cells as germ-line cells in next generation
  • What is a "phenotype" ?

    The observable characteristics of an organism are produced by the genotype and its interaction with the environment
  • What is a "genotype" ?

    The complete genetic make up (allele composition) of an organism
  • What is a "nonsense mutation" ?

    A base pair change alters an mRNA codon for an amino acid to a stop (nonsense) codon
    • UAG
    • UAA
    • UGA
  • What is a "neutral mutation" ? (2)

    • Base pair change in a gene that changes a mRNA codon in a way that the resulting amino acid substitution results no detectable change in the function of the protein being translated
    • Subset of missense mutations that does not result in a change of the protein
  • What is a "silent mutation" ? (3)

    • Synonymous mutation
    • Changes a base pair but the altered mRNA codon specifies the same amino acid in the protein
    • Happens often on the 3rd position of a codon
  • What is a "frameshift mutation" ? (3)

    • If 1 or more base pairs are added or deleted from a protein coding gene
    • the reading frame of an mRNA can change downstream of the mutation

    Usually results in a non-functioning protein
    • Stopcodon
    • Polypeptide too long
    • Significant alteration of amino acid sequence
  • How can mutations be classified? (3)

    Cause: 
    • spontaneous vs. induced

    Effect on DNA: 
    • point vs. chromosomal
    • substitution vs. insertion/deletion
    • transition vs. transversion

    Effect on an encoded protein:
    • Nonsense
    • Missense
    • Neutral
    • Silent
    • Frameshift
  • 7.1.3 Spontaneous and induced mutations

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  • Characteristics of DNA replication errors? (5)

    • base pair substitution mutations
    • point mutation
    • change of one base pair to another
    • mismatched base pairs during replication
    • enol form of base (instead of keto form)
    • Repair by "mismatch repair systems"
  • What is a "tautomer" ? (2)

    • Alternate chemical forms in which DNA or RNA bases can exist
    • Keto (normal) --> Enol (rare) 
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