Exam 7: Gene Expression and Control

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What does it mean that the genetic code is "highly conserved"?

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A

  In the figure above, the process indicated by number 1 is _____, while the process indicated by number 2 is _____. In the figure above, the process indicated by number 1 is _____, while the process indicated by number 2 is _____.

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C

Which RNA acts as an enzyme?

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B

Many ribosome-inactivating proteins are not toxic to humans because _____.

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Which of the following carries amino acids to ribosomes?

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Transcription factors bind to _____.

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Internationally, the use of ricin as a weapon is banned in most countries according to the ____.

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In sickle cell anemia, what happens to the hemoglobin molecule that causes the red blood cell to sickle?

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Eukaryotic post-transcriptional modifications occur in the _____.

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During elongation, ribosomes catalyze formation of a ____ bond between an amino acid and the growing polypeptide.

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A ribosome contains _____.

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Mutations in an exon region of a gene are most likely to _____.

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Match each term with the most appropriate description.
Premises:
a tRNA triplet complementary to a mRNA codon
Responses:
translation
anticodon
rRNA
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Premises:
Responses:
a tRNA triplet complementary to a mRNA codon
translation
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Which process is responsible for the conversion of DNA information into messenger RNA?

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As the polypeptide is elongating during translation, what is the ribosome doing?

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Transcription starts at a region of DNA called a(n)_____.

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The difference between normal and sickle-cell hemoglobin is _____.

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The activity of the ribosome in translation is analogous to a(n)_____.

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How many different amino acids are found in humans?

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Identify the type of mutation associated with the following questions and statements. Some answers may be used more than once.
Premises:
Which type of mutation replaces glutamic acid with valine in beta globin proteins in individuals with sickle-cell anemia?
Responses:
Base-pair substitution
Deletion only
Frame-shift mutation
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Premises:
Responses:
Which type of mutation replaces glutamic acid with valine in beta globin proteins in individuals with sickle-cell anemia?
Base-pair substitution
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