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Ch. 20 - Recombinant DNA Technology
Klug - Concepts of Genetics  12th Edition
Klug12th EditionConcepts of Genetics ISBN: 9780135564776Not the one you use?Change textbook
Chapter 20, Problem 7

Restriction sites are palindromic; that is, they read the same in the 5' to 3' direction on each strand of DNA. What is the advantage of having restriction sites organized this way?

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Understand that DNA is double-stranded and antiparallel, meaning one strand runs 5' to 3' and the complementary strand runs 3' to 5'.
Recognize that a palindromic restriction site reads the same 5' to 3' on both strands, which means the sequence is symmetrical when read in the correct direction on each strand.
Consider how restriction enzymes, which cut DNA at specific sequences, interact with double-stranded DNA. The palindromic nature allows the enzyme to recognize and bind to the same sequence on both strands simultaneously.
Realize that this symmetry ensures the enzyme can make precise cuts at the same position on both strands, producing consistent and predictable fragments.
Conclude that the advantage of palindromic restriction sites is that they facilitate accurate and efficient cutting by restriction enzymes, which is essential for molecular cloning and DNA analysis.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Restriction Enzymes and Recognition Sites

Restriction enzymes are proteins that cut DNA at specific sequences called restriction sites. These sites are typically short, specific sequences where the enzyme binds and cleaves the DNA, enabling precise cutting for molecular cloning and genetic analysis.
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Palindromic DNA Sequences

A palindromic DNA sequence reads the same 5' to 3' on one strand and 5' to 3' on the complementary strand. This symmetry allows restriction enzymes to recognize and bind to both strands simultaneously, ensuring accurate and efficient cutting.
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Advantages of Palindromic Restriction Sites

Palindromic restriction sites enable restriction enzymes to produce consistent and predictable cuts, often generating sticky or blunt ends. This facilitates the joining of DNA fragments during cloning, improving the efficiency of recombinant DNA technology.
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Related Practice
Textbook Question

The human insulin gene contains a number of sequences that are removed in the processing of the mRNA transcript. In spite of the fact that bacterial cells cannot excise these sequences from mRNA transcripts, explain how a gene like this can be cloned into a bacterial cell and produce insulin.

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Textbook Question

Although many cloning applications involve introducing recombinant DNA into bacterial host cells, many other cell types are also used as hosts for recombinant DNA. Why?

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Textbook Question

Using DNA sequencing on a cloned DNA segment, you recover the nucleotide sequence shown below. Does this segment contain a palindromic recognition sequence for a restriction enzyme? If so, what is the double-stranded sequence of the palindrome, and what enzyme would cut at this sequence?

CAGTATGGATCCCAT

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Textbook Question

List the advantages and disadvantages of using plasmids as cloning vectors. What advantages do BACs and YACs provide over plasmids as cloning vectors?

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Textbook Question

What are the advantages of using a restriction enzyme whose recognition site is relatively rare? When would you use such enzymes?

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Textbook Question

In 1975, the Asilomar Conference on Recombinant DNA was organized by Paul Berg, a pioneer of recombinant DNA technology, at a conference center at Asilomar State Beach in California. Physicians, scientists, lawyers, ethicists, and others gathered to draft guidelines for safe applications of recombinant DNA technology. These general guidelines were adopted by the federal government and are still in practice today. Consider the implications of recombinant DNA as a new technology. What concerns might the scientific community have had then about recombinant DNA technology? Might those same concerns exist today?

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