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
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7 DNA mutation, DNA repair and transposable elements
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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
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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
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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
- 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
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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
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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
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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
- spontaneous vs. induced
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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"
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What is a "tautomer" ? (2)
- Alternate chemical forms in which DNA or RNA bases can exist
- Keto (normal) --> Enol (rare)
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