Chapter 20: DNA Technology
AP Biology
Stoneleigh-Burnham School
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Judith S. de Nuño
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Chapter Objectives

    1. Explain how advances in recombinant DNA technology have helped scientists study the eukaryotic genome
    2. Describe the natural function of restriction enzymes
    3. Describe how restriction enzymes and gel electrophoresis are used to isolate DNA fragments
    4. Explain how the creation of sticky ends by restriction enzymes is useful in producing a recombinant DNA molecule
    5. Outline the procedures for producing plasmid and phage vectors
    6. Explain how vectors are used in recombinant DNA technology
    7. List and describe the 2 major sources of genes fro cloning
    8. Describe the function of reverse transcriptase in retroviruses and explain how they are useful in recombinant DNA technology
    9. Describe ho genes of interest can be identified with the use of a probe
    10. Explain the importance of DNA synthesis and sequencing to modern studies of eukaryotic genomes
    11. Describe how bacteria can be induced to produce eukaryotic gene products
    12. List some advantages for using yeast in the production of gene products
    13. List and describe 4 complementary approaches used to map the human genome
    14. Explain how RFLP analysis and PCR can be applied to the Human Genome Project
    15. Describe how recombinant DNA technology can have medical applications such as diagnosis of genetic disease, development of gene therapy, vaccine production, and development of pharmaceutical products
    16. Describe how gene manipulation has practical applications for agriculture
    17. Describe ho plant genes can be manipulated using the Ti plasmid carried by Agrobacterium as a vector
    18. Explain how foreign DNA may be transferred into o monocotyledonous plants
    19. Describe how recombinant DNA studies and the biotechnology industry are regulated with regards to safety and policy matters

 

Chapter Terms:

genetic engineering

recombinant DNA

biotechnology

nucleic acid probe

gene cloning

restriction enzymes

antisense nucleic acid

restriction fragments length polymorphisms (RFLPs)

cloning vector

nucleic acid hybridization

denaturation

expression vector

restriction site

complementary DNA (cDNA)

electroporation

genomic library

cDNA library

polymerase chain reaction (PCR)

in vitro mutagenesis

gel electrophoresis

Southern blotting

restriction fragment

artificial chromosomes

in situ hybridization

Ti plasmid

Human Genome Project

chromosome walking

DNA microarray assays

vaccine

DNA fingerprint simple tandem repeats (STRs)

 

Chapter Outline Framework

  1. DNA Cloning
    1. DNA technology makes it possible to clone genes for basic research and commercial applications
    2. Restriction enzymes are used to make recombinant DNA
    3. Genes can be cloned in recombinant DNA vectors
    4. Cloned genes are stored in DNA libraries
    5. The polymerase chain reaction (PCR) clones DNA entirely in vitro
  2. Analysis of Cloned DNA
    1. Restriction fragment analysis detects DNA differences that affect restriction sites
    2. Entire genomes can be mapped at the DNA level
  3. Practical Applications of DNA Technology
    1. DNA technology is reshaping medicine and the pharmaceutical industry
    2. DNA technology offers forensic, environmental, and agricultural applications
    3. DNA technology raises important safety and ethical questions

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