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Genetic Technology

Explore the world of genetic engineering and recombinant DNA technology to increase allele frequencies in populations. Learn about transgenic organisms, restriction enzymes, vectors, gene cloning, and animal cloning techniques. Discover the process of inserting foreign DNA into vectors and transferring them into host cells for rapid reproduction and gene replication. Delve into the history of animal cloning and the potential benefits and challenges associated with genetic manipulation. Uncover the advancements and limitations of genetic technology in the realm of DNA manipulation.

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Genetic Technology

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  1. Genetic Technology

  2. Section 13.2 Summary – pages 341 - 348 Genetic Engineering • 1. Genetic engineering is a faster and more reliable method for increasing the frequency of a specific allele in a population by cutting fragments of DNA from one organismand inserting the fragments into a host organism of the same or a different species.

  3. (It is a way to increase the frequency of a specific allele by putting pieces of DNA from one organism into another)

  4. Section 13.2 Summary – pa341 - 348 Genetic Engineering • 2. You also may hear genetic engineering referred to as recombinantDNA technology. • 3. Recombinant DNA is made by connecting or recombining, fragments of DNA from different sources.

  5. Section 13.2 Summary – pages 341 - 348 Transgenic organisms contain recombinant DNA • 4. Plants and animals that contain functional recombinant DNA from an organism of a different type are known as transgenic organisms because they contain foreign DNA.

  6. Section 13.2 Summary – pages 341 - 348 5. Transgenic organisms contain recombinant DNA • The first step of the process is to isolate the foreign DNA fragment that will be inserted. • The second step is to attach the DNA fragment to a carrier. • The third step is the transfer into the host organism.

  7. Section 13.2 Summary – pages 341 - 348 Restriction enzymes cleave (cut) DNA • To isolate a DNA fragment, small pieces of DNA must be cut from a chromosome. • 6. Restriction enzymes are bacterial proteins that have the ability to cut both strands of the DNA molecule at a specific nucleotide sequence.

  8. Section 13.2 Summary – pages 341 - 348 Cut Cleavage Restriction enzymes cleave (cut) DNA Insertion Sticky ends

  9. Section 13.2 Summary – pages 341 - 348 Vectors transfer DNA • 7. A vector is the means by which DNA from another species can be carried into the host cell. • Vectors may be biological or mechanical.

  10. Section 13.2 Summary – pages 341 - 348 Vectors transfer DNA • 8. Biological vectors include viruses and bacterial plasmids. • 9. A plasmid, is a small ring of DNA found in a bacterial cell.

  11. Vectors transfer DNA • 10. Two types of mechanical vectors carry foreign DNA into a cell’s nucleus

  12. Section 13.2 Summary – pages 341 - 348 Vectors transfer DNA • One, a micropipette, is inserted into a cell;. the other is a microscopic metal bullet coated with DNA that is shot into the cell from a gene gun

  13. Section 13.2 Summary – pages 341 - 348 Insertion into a vector • If a plasmid and foreign DNA have been cleaved with the same restriction enzyme, the ends of each will match and they will join together, reconnecting the plasmid ring. • The foreign DNA is recombined into a plasmid or viral DNA with the help of a second enzyme.

  14. Section 13.2 Summary – pages 341 - 348 Gene cloning • After the foreign DNA has been inserted into the plasmid, the recombined DNA is transferred into a bacterial cell. • 11. An advantage to using bacterial cells to clone DNA is that they reproduce quickly; therefore, millions of bacteria are produced and each bacterium contains hundreds of recombinant DNA molecules.

  15. Section 13.2 Summary – pages 341 - 348 Gene cloning • 12. Clones are genetically identical copies. • Plasmids also can be used to deliver genes to animal or plant cells, which incorporate the recombinant DNA.

  16. Section 13.2 Summary – pages 341 - 348 Gene cloning • 13. Each time the host cell divides it copies the recombinant DNA along with its own.

  17. Section 13.2 Summary – pages 341 - 348 Gene cloning Recombined DNA Foreign DNA (gene for human growth hormone) Cleavage sites Recombined plasmid Bacterial chromosome E. coli Plasmid Human growth hormone

  18. Section 13.2 Summary – pages 341 - 348 Cloning of animals • Although their techniques are inefficient, scientists are coming closer to perfecting the process of cloning animals.

  19. What animals have been cloned? • Scientists have been cloning animals for many years. • In 1952, the first animal, a tadpole, was cloned. • Dolly the Sheep was cloned in 1997. • www.ornl.gov/sci/techresources/Human_Genome/elsi/cloning.shtml#animalsQ

  20. Before the creation of Dolly, the first mammal cloned from the cell of an adult animal, clones were created from embryonic cells. • Since Dolly, researchers have cloned a number of large and small animals including sheep, goats, cows, mice, pigs, cats, and rabbits. All these clones were created using nuclear transfer technology. • Hundreds of cloned animals exist today, but the number of different species is limited. Attempts at cloning certain species have been unsuccessful.

  21. The most productive and useful plants and animals can be cloned to help humans. • The drawback is using older DNA because it will have accumulated damage over the years. The clone will likely show signs of age early.

  22. In the Star Wars movies, all of the storm troopers were clones of this one indidual who was a good soldier. This is science fiction, but the application is the same.

  23. Section 13.2 Summary – pages 341 - 348 Polymerase chain reaction • 14. A method called polymerase chain reaction (PCR) has been developed in order to replicate DNA outside living organisms, • This method uses heat to separate DNA strands from each other.

  24. Genetic markers are a known location of a gene, which is used as a reference point to describe the location of other genes.

  25. Section 13.2 Summary – pages 341 - 348 Polymerase chain reaction • The machine repeatedly replicates the DNA, making millions of copies in less than a day.

  26. Section 13.2 Summary – pages 341 - 348 Sequencing DNA • In DNA sequencing, millions of copies of a double-stranded DNA fragment are cloned using PCR. Then, the strands are separated from each other. • The single-stranded fragments are placed in four different test tubes, one for each DNA base.

  27. Section 13.2 Summary – pages 341 - 348 Sequencing DNA • Each tube contains four normal nucleotides (A,C, G,T) and an enzyme that can catalyze the synthesis of a complementary strand. • One nucleotide in each tube is tagged with a different fluorescent color. • The reactions produce complementary strands of varying lengths.

  28. Section 13.2 Summary – pages 341 - 348 Sequencing DNA • 15. These strands are separated according to size by 16. gelelectrophoresis producing a pattern of fluorescent bands in the gel. • The bands are visualized using a laser scanner or UV light.

  29. Section 13.2 Summary – pages 341 - 348 Gel Electrophoresis • Restriction enzymes are the perfect tools for cutting DNA. However, once the DNA is cut, a scientist needs to determine exactly what fragments have been formed..

  30. Section 13.2 Summary – pages 341 - 348 Restriction enzymes • Either one or several restriction enzymes is added to a sample of DNA. The restriction enzymes cut the DNA into fragments. DNA fragments

  31. Section 13.2 Summary – pages 341 - 348 The gel • With a consistency that is firmer than dessert gelatin, the gel is molded so that small wells form at one end. Gel • DNA fragments are placed into small wells at the end of a firm block of gel.

  32. Section 13.2 Summary – pages 341 - 348 Power source An electric field • The gel is placed in a solution and an electric field is applied. One end of the gel is positive and the other end is negative. Negative end Positive end

  33. Section 13.2 Summary – pages 341 - 348 The fragments move • The negatively charged DNA fragments travel toward the positive end. Completed gel Shorter fragments Longer fragments

  34. Section 13.2 Summary – pages 341 - 348 The fragments move • 18.The smaller the fragment, the faster it moves through the gel. • The smallest fragments move the farthest from the well.

  35. Making a Gel (summarized)(#17) • 1. Restriction enzymes cut DNA into fragments • 2. DNA fragments are placed into small wells at the end of a firm block of gel which glows under UV light. • 3. One end of the gel is made + (pos.) and the other – (neg.) • 4. Neg. charged DNA fragments move toward the + end.

  36. Section 13.2 Summary – pages 341 - 348 Applications of DNA Technology • The main areas proposed for recombinant bacteria are in industry, medicine, and agriculture. Recombinant DNA in industry • Many species of bacteria have been engineered to produce chemical compounds used by humans.

  37. Section 13.2 Summary – pages 341 - 348 19.Recombinant DNA in industry • Scientists have modified the bacterium E. coli to produce the expensive indigo dye that is used to color denim blue jeans.

  38. Section 13.2 Summary – pages 341 - 348 19. Industrial Applications of DNA Technology • The production of • cheese • paper • laundry detergents • sewage treatment

  39. Section 13.2 Summary – pages 341 - 348 20. Recombinant DNA in medicine • Pharmaceutical companies already are producing molecules made by recombinant DNA to treat human diseases. • Recombinant bacteria are used in the production of human growth hormone to treat pituitary dwarfism and insulin to treat diabetes.

  40. Section 13.2 Summary – pages 341 - 348 20. Recombinant DNA in medicine • Scientists can study diseases and the role specific genes play in an organism by using transgenic animals

  41. Section 13.2 Summary – pages 341 - 348 21. Transgenic animals • . An animal that contains recombinant DNA from other organisms inserted into them is called a transgenic organism.

  42. Section 13.2 Summary – pages 341 - 348 Transgenic animals • Mouse chromosomes also are similar to human chromosomes. • Scientists know the locations of many genes on mouse chromosomes.

  43. Section 13.2 Summary – pages 341 - 348 Transgenic animals • On the same farm in Scotland that produced the cloned sheep Dolly, a transgenic sheep was produced that contained the corrected human gene for hemophilia A. • This human gene inserted into the sheep chromosomes allows the production of the clotting protein in the sheep’s milk.

  44. Section 13.2 Summary – pages 341 - 348 22. Recombinant DNA in agriculture • Recombinant DNA technology has been highly utilized in the agricultural and food industries. • Crops have been developed that are better tasting, stay fresh longer, and are protected from disease and insect infestations.

  45. Section 13.2 Summary – pages 341 - 348 Recombinant DNA in agriculture The Most Common Genetically Modified (GM) Crops 150 140 Millions of hectares 7% 100 72 36% 50 34 25 16% 11% 0 Soybeans Corn Cotton Canola

  46. Section 13.3 Summary – pages 349 - 353 23. Mapping and Sequencing the Human Genome • In 1990, scientists in the United States organized the Human Genome Project (HGP). It is an international effort to completely map and sequence the human genome, the approximately 35 000-40 000 genes on the 46 human chromosomes. • The human genome map shows the sequence of the genes on the 46 chromosomes.

  47. Linkage Maps show the positions of known genes on a chromosome.

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