Genetic Analysis: An Integrated Approach (2nd Edition)
Genetic Analysis: An Integrated Approach (2nd Edition)
2nd Edition
ISBN: 9780321948908
Author: Mark F. Sanders, John L. Bowman
Publisher: PEARSON
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Chapter 12, Problem 30P

A geneticist searching for mutations uses the restriction endonucleases SmaI and PvuII to search for mutations that eliminate restriction sites. SmaI will not cleave DNA with CpGmethylation. It cleaves DNA at the restriction digestion sequence

Chapter 12, Problem 30P, A geneticist searching for mutations uses the restriction endonucleases SmaI and PvuII to search for , example  1

5'-CCC GGG-3'

3'-GGG CCC-5'

Chapter 12, Problem 30P, A geneticist searching for mutations uses the restriction endonucleases SmaI and PvuII to search for , example  2

PvuII is not sensitive to CpG methylation. It cleaves DNA at the restriction sequence

Chapter 12, Problem 30P, A geneticist searching for mutations uses the restriction endonucleases SmaI and PvuII to search for , example  3

5'-CAG CTG-3'

3'-GTC GAC-5'

Chapter 12, Problem 30P, A geneticist searching for mutations uses the restriction endonucleases SmaI and PvuII to search for , example  4

a. What common feature do SmaI and PvuII share that would be useful to a researcher searching for mutations that disrupt restriction digestion?

b. What process is the researcher intending to detect with the use of these restriction enzymes?

c. Explain why CpG dinucleotides are hotspots of mutation.

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The recognition sequence for the restriction enzyme TaqI is T↓CGA. Indicate the products of the reaction of TaqI with the DNA sequence shown.
Given the following double-stranded fragment of DNA: 5'- ACTTGGCAGGCCTTCGATCC-3' 3'- TGAАССGTCСGGAAGCTAGG-5' A hypothetical restriction endonuclease recognizes a 6bp sequence with two-fold symmetry (typical for restriction enzymes) found in this fragment and catalyzes cleavage of this DNA on both strands between GG nucleotides within the recognition sequence. This nuclease exhibits b-type cleavage (atypical for restriction enzymes). Draw the double-stranded sequence of each fragment after cleavage showing any phosphates left on the ends.
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Genetic Analysis: An Integrated Approach (2nd Edition)

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