Biology: The Dynamic Science (MindTap Course List)
Biology: The Dynamic Science (MindTap Course List)
4th Edition
ISBN: 9781305389892
Author: Peter J. Russell, Paul E. Hertz, Beverly McMillan
Publisher: Cengage Learning
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Chapter 18, Problem 9TYK
Summary Introduction

Introduction:

Restriction fragment length polymorphism (RFLP) is a molecular technique which is used to identify the differences in DNA (deoxyribonucleic acid) sequences between individuals. The restriction endonuclease is used for cutting the nucleotides at different restriction sites on the DNA, which differentiate bands between two individuals after electrophoresis.

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Certain restriction endonucleases produce cohesive (sticky) ends.  This means that they: a. stick tightly to the ends of the DNA they have cut. b. cut both DNA strands at the same base pair. c.   make a staggered double-strand cut, leaving ends with a few nucleotides of single-stranded DNA protruding.   d. cut in regions of high GC content, leaving ends that can form more hydrogen bonds than ends of high AT content. e. cut in regions of high AT content, leaving ends that can form more hydrogen bonds than ends of high GC content.
The same restriction endonuclease must be used to excise the foreign DNA and bacterial DNA. Select one: True False   Why? Select one: a. It must use different restriction endonucleases because the bacterial and foreign DNA sequences are different. b. It must use same restriction endonuclease so that the restriction sites are identical in both foreign and bacterial DNA. c. It must use same restriction endonuclease so that the restriction sites are different in both foreign and bacterial DNA. d. It must use different restriction endonucleases because the bacterial and foreign DNA sequences are exactly the same.
RELPs: A. are the same length for mutant and normal beta-globin alleles.  b. determine the sequence of bases in a DNA fragment.  c. have short, palindromic sequences of DNA in the middle.  D. are used as vectors. e. are produced by reaction with restriction enzymes and are detected with PCR and gel electrophoresis.
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