Exam 15: Gene Mutation and Molecular Medicine

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The addition of _______ groups to their DNA is one method used by bacteria to prevent their own DNA from being cut by restriction enzymes.

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methyl

An example of a gain of function missense mutation is a mutation of the TP53 gene. Normally, this protein inhibits cell division, but certain mutations in the TP53 gene

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A

The study of allele-specific cleavage differences detects genetic diseases by examining patterns of activity of _______ enzymes.

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restriction

In one type of cancer, myelogenous leukemia, certain white blood cells undergo a gain-of-function mutation resulting in a totally new protein. The treatment involves

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Which of the following mutations is not a chromosomal mutation?

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Individuals with PKU have an abnormal

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Sickle-cell disease is an inherited disease caused by an alteration of a single amino acid in a protein. Specifically,

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Genetic diagnosis by DNA testing

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Which of the following types of variation involves changes at a single nucleotide base?

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Gel electrophoresis

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Which of the following statements regarding short tandem repeats (STRs) is false?

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Restriction fragment banding patterns

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Nitrites, a human-made preservative for meats, and aflatoxin, a natural product produced by the mold Aspergillus, are similar in that

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You have characterized over 100 mutations in a partic-ular gene that are linked to a certain disease. The mutations you have identified are all due to a single base change in one codon of the gene encoding protein X. Which DNA technique would you use to analyze patients who might have this disease?

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Which of the following types of variations would be most detectable by gel electrophoresis if the differences in the DNA were between two recognition sites for a restriction enzyme?

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For gene therapy to be most effective, genes should

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The type of mutation that stops translation of a protein results in a shortened protein because translation does not proceed beyond the mutation. An example is thalassemia, which is

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An RFLP

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Most restriction sites are _______ base pairs long.

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A genetic disease that is caused by a deletion in the X chromosome is

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