Study Guide And Solutions Manual For Genetic Analysis: An Integrated Approach
Study Guide And Solutions Manual For Genetic Analysis: An Integrated Approach
3rd Edition
ISBN: 9780134832258
Author: Mark F. Sanders, John L. Bowman, Peter Mirabito
Publisher: PEARSON
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Chapter 12, Problem 25P

What is the likely effect of each of the following mutations of the trpLregion on attenuation control of trp operon gene transcription? Explain your reasoning.

a. Region 3 is deleted.

b. Region 4 is deleted.

c. The entire trpL region is deleted.

d. The start (AUG) codon of the trpL polypeptide is deleted.

e. Two nucleotides are inserted into the trpLregion immediately after the polypeptide stop codon.

f. Twenty nucleotides are inserted into the trpLregion immediately after the polypeptide stop codon.

g. Ten nucleotides are inserted between regions 2 and 3 of trpL .

h. Two nucleotides are inserted immediately following the polypeptide start codon

i. The entire polypeptide coding sequence of trpLis deleted.

j. The eight uracil nucleotides immediately following region 4 are deleted.

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Students have asked these similar questions
. a. How many ribosomes are required (at a minimum)for the translation of trpE and trpC from a singletranscript of the trp operon?b. How would you expect deletion of the two tryptophan codons in the RNA leader to affect theexpression of the trpE and trpC genes?
Gene expression in bacteria is controlled by the operon model.  a) Why is the operon model important? b) Why is the trp operon known as a repressible operon?
You have isolated two different mutants (reg1 and reg2) causing constitutive expression of the emu operon (emu1 emu2). One mutant contains a defect in a DNA-binding site, and the other has a loss-of-function defect in the gene encoding a protein that binds to the site. Is the DNA-binding protein a positive or negative regulator of gene expression? Explain. To determine which mutant has a defect in the site and which one has a mutation in the binding protein, you decide to do an analysis using F′ plasmids. Assuming you can assay levels of the Emu1 and Emu2 proteins, what results do you predict for the two strains (i and ii; see descriptions below) if reg2 encodes the regulatory protein and reg1 is the regulatory site? Explain. F′ (reg1− reg2+ emu1− emu2+)/reg1+ reg2+ emu1+ emu2− F′ (reg1+ reg2− emu1− emu2+)/reg1+ reg2+ emu1+ emu2−

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Study Guide And Solutions Manual For Genetic Analysis: An Integrated Approach

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