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DNA Manipulation Techniques: Cutting and Copying

Learn about the ways to manipulate DNA, including cutting it with restriction enzymes and copying specific sequences through Polymerase Chain Reaction (PCR). Explore the use of restriction maps and gel electrophoresis in genetic engineering and mutation studies.

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DNA Manipulation Techniques: Cutting and Copying

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  1. Ways to Manipulate DNA • CUTTING

  2. Restriction enzymes cut DNA. • Restriction enzymes act as “molecular scissors.” • come from various types of bacteria • allow scientists to more easily study and manipulate genes • cut DNA at a specific nucleotide sequence called a restriction site

  3. Different restriction enzymes cut DNA in different ways. • each enzyme has a different restriction site

  4. Restriction maps show the lengths of DNA fragments. • Gel electrophoresis is used to separate DNA fragments by size. • A DNA sample is cut with restriction enzymes. • Electrical current pulls DNA fragments through a gel.

  5. Smaller fragments move faster and travel farther than larger fragments. • Fragments of different sizes appear as bands on the gel.

  6. A restriction map shows the lengths of DNA fragments between restriction sites. • only indicate size, not DNA sequence • useful in genetic engineering • used to study mutations

  7. Ways to manipulate DNA • Copying

  8. target sequence of DNA PCR uses polymerases to copy DNA segments. • PCR makes many copies of a specific DNA sequence in a few hours. • PCR amplifies DNA samples. • PCR is similar to DNA replication.

  9. DNA strands primer1 polymerase primer 2 nucleotides PCR is a three-step process. • PCR uses four materials. • DNA to be copied • DNA polymerase • A, T, C, and G nucleotides • two primers

  10. DNA strands primer1 polymerase primer 2 nucleotides • The three steps of PCR occur in a cycle. • heat is used to separate double-stranded DNA molecules • primers bind to each DNA strand on opposite ends of the segment to be copied • DNA polymerase binds nucleotides together to form new strands of DNA

  11. Each PCR cycle doubles the number of DNA molecules.

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