GENETIC ANALYSIS: AN INTEG. APP. W/MAS
GENETIC ANALYSIS: AN INTEG. APP. W/MAS
2nd Edition
ISBN: 9781323142790
Author: Sanders
Publisher: Pearson Custom Publishing
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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 map of plasmid pUC19 is shown below.  The restriction site coordinate is the position of the 5’base on the top strand of each site sequence.  The restriction enzyme sites are in bold type if there is only one site in pUC19. Please list the fragments in order of size, largest to smallest, which will result from a complete digestion by the restriction enzyme PvuII. Please list the fragments in order of size, largest to smallest, which will result from a complete digestion by the restriction enzyme DrdI.
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.
This is a restriction map for the 250 base pair plasmid pSage. Restriction sites for the restriction endonuclease Nhel are 7, 69 and 160. What are the sizes of the restriction fragments produced? Check all that apply. p SAGE Nhel 7 250 bp Nhền 160 Nhel 69 62 69 91 160 97

Chapter 12 Solutions

GENETIC ANALYSIS: AN INTEG. APP. W/MAS

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