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Essential Cell Biology 5th edition

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Questions

293

• MicroRNAs (miRNAs) control gene expression by base-pairing with

specific mRNAs and inhibiting their stability and translation.

• Cells have a defense mechanism for destroying “foreign” doublestranded

RNAs, many of which are produced by viruses. It makes use

of small interfering RNAs (siRNAs) that are produced from the foreign

RNAs in a process called RNA interference (RNAi).

• The recent discovery of thousands of long noncoding RNAs in

mammals has revealed new roles for RNAs in assembling protein

complexes and regulating gene expression.

KEY TERMS

cell memory

combinatorial control

differentiation

DNA methylation

epigenetic inheritance

gene expression

induced pluripotent stem

(iPS) cells

long noncoding RNA

microRNA (miRNA)

positive feedback loop

post-transcriptional control

promoter

regulatory DNA sequence

regulatory RNA

reporter gene

RNA interference (RNAi)

small interfering RNA (siRNA)

transcription regulator

transcriptional activator

transcriptional repressor

QUESTIONS

QUESTION 8–4

A virus that grows in bacteria (bacterial viruses are called

bacteriophages) can replicate in one of two ways. In the

prophage state, the viral DNA is inserted into the bacterial

chromosome and is copied along with the bacterial genome

each time the cell divides. In the lytic state, the viral DNA

is released from the bacterial chromosome and replicates

many times in the cell. This viral DNA then produces viral

coat proteins that together with the replicated viral DNA

form many new virus particles that burst out of the bacterial

cell. These two forms of growth are controlled by two

transcription regulators, the repressor (product of the cI

gene) and Cro, both of which are encoded by the virus. In

the prophage state, cI is expressed; in the lytic state, Cro is

expressed. In addition to regulating the expression of other

genes, cI represses the Cro gene, and Cro represses the cI

gene (Figure Q8–4). When bacteria containing a phage in

the prophage state are briefly irradiated with UV light, cI

protein is degraded.

A. What will happen next?

B. Will the change in (A) be reversed when the UV light is

switched off?

C. What advantage might this response to UV light provide

to the virus?

Figure Q8–4

cI gene

PROPHAGE

STATE

cI gene

Cro protein

NO cI GENE

TRANSCRIPTION

cI protein

Cro gene

NO Cro GENE

TRANSCRIPTION

Cro gene

LYTIC

STATE

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