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True/False
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Multiple Choice
A) transcriptionally.
B) translationally.
C) posttranslationally.
D) at any point on the enzymatic production pathway.
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Multiple Choice
A) activity of a catabolite repressor protein on multiple pathways
B) antisense RNA silencing
C) feedback inhibition with allosteric proteins
D) presence of corepressors and inducers which are molecules undetected by transcriptomics
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Multiple Choice
A) attenuation
B) feedback inhibition
C) riboswitches
D) transcription factors
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Multiple Choice
A) the varied strengths metabolite-regulating compounds can have with the enzyme such as hydrogen bonding, covalent bonding, and van der Waals attractions.
B) having multiple independently functional subunits.
C) the structural strength enzymes have once properly folded compared to short-lived and easily degradable transcripts during translational regulation.
D) weak chemical modifications of the enzyme rather than harsh protein-protein or protein-DNA interactions.
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True/False
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True/False
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Multiple Choice
A) Advanced 3D modeling techniques of mRNA folding would be necessary because complementary nucleotide binding predictions would not be useful.
B) Locate short regions of an individual transcript with several complementary sites.
C) Identify homologous sRNAs in other organisms.
D) Identify several complementary mRNAs encoded in the genome.
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Multiple Choice
A) activators
B) activators and inducers
C) repressors
D) repressors and corepressors
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True/False
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Multiple Choice
A) major groove
B) minor groove
C) histone complex
D) primary supercoil
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Multiple Choice
A) lag phase
B) early to middle log phase
C) late log to early stationary phase
D) middle to late stationary phase
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