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AP Bio: Ch.20: DNA Technology and Genomics Flashcards

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1158754357genetic engineeringthe process of manipulating genes and genomes0
1158754358biotechnologythe process of manipulating organisms or their components for the purpose of making useful products1
1158754359restriction enzymesused to cut strands of DNA at specific locations (called restriction sites/sequences); they are derived from bacteria2
1158754360when a DNA molecule is cut by restriction enzymes, the result will always be a set ofrestriction fragments which will have at least one single-stranded end, called a sticky-end3
1158754361sticky-ends can formhydrogen bonds with complementary single-stranded pieces of DNA; these unions can be sealed with the enzyme DNA Ligase4
1158754362recombinant DNADNA that is artificially made, using DNA from different sources--and often different species; for example: the introductions of a human gene into an E. Coli bacterium5
1158754363gene cloningthe process where scientists can produce multiple copies of specific segments of DNA; they can then work within the lab6
1158754364plasmidsextra small, circular, double-stranded pieces of DNA found in viral, yeast, or bacterial cells used extensively in biotechnology and recombinant DNA7
1158754365the plasmids serve as a"vehicle" for transporting genes from one organism to another (transformation) so multiple copies can be made (gene cloning)8
1158754366gene cloning yieldsmultiple copies of a gene or other DNA segments9
1158754367the cloning of DNA occurs in how many steps510
1158754368step 1identify and isolate the gene of interest and a cloning vector; the vector of the plasmid (usually bacterial) that will carry the DNA sequence to be cloned11
1158754369step 2cut both the gene of interest and the vector with the same restriction enzyme; this gives the plasmid and the human gene matching sticky-ends12
1158754370step 3join the 2 pieces of DNA from recombinant plasmids by mixing the plasmids with the DNA fragments; the human DNA fragments can be sealed into the plasmid using DNA ligase13
1158754371step 4get the plasmid vector carrying the gene of interest into the host cell; the plasmids are taken up by bacterium by transformation14
1158754372step 5select for cells that have been transformed; the bacterial cels carrying the clones must be identified or selected; this can be done by linking the gene to an antibiotic resistance gene or a reporter gene such as GFP (green flourescent protein)15
1158754373In the transformation lab, we will useampicillin-resistant plasmid; any bacterial cells that did not pick up the plasmid by transformation will be killed when grown on agar with the antibiotic ampicillin16
1158754374what are 3 example applicationsinsulin production, human growth hormone production, and the production of other proteins that make crops resistant to pests17
1163508300gene can't be above a certain size or a plasmidwon't work18
1163508301mRNA must not need splicing to remove introns becausewe are placing it directly into a cell to be expressed (bacteria can't remove introns19
1163508302but if we still want a bacterial cell to make a human protein that does not need mRNA processing, we can make acDNA copy of the gene and insert that instead20
1163508303cDNA is created usingreverse transcriptase to turn a processed mRNA (coding for a certain protein) back into a DNA to insert into the bacterial plasmid21
1163508304another biotechnology tool we use isPCR22
1163508305PCR (polymerase chain reaction)a method used to greatly amplify a particular piece of DNA without the use of cell23
1163508306PCR is used to amplify DNA when the source isimpure or scanty (as it would be at a crime scene--a little amount of DNA)24
1163508307what are the steps for PCRheat up, add primer, add Taq polymerase and let it cool to continue the cycle to make more copies25
1163508308Taq polymerase is good at withstandinghigh temperatures26
1163508309DNA technology allows us to study thesequence, expression, and function of a gene27
1163508310Gel electrophoresisa lab technique that is used to separate macromolecules (anything with a negative charge), primarily DNA and proteins, on the basis of their size and charge with the use of an electrical current28
1163618296in separating DNA, (that has been cut into fragments with restriction enzymes), the negative charges on phosphates in the molecule cause DNA tomove more toward the positive pole29
1163618297the gel allows smaller molecules to movemore easily than larger fragments of DNA. The DNA fragments are separated by size30
1163618298you have to use the _______restriction enzyme on eachsmall; person31
1163618299the smaller the fragment, thefaster it moves down32
1163618300the dye is used tovisualize the fragments of DNA33
1163618301what are 3 forensic applicationslinks suspect bodily to the crime scene, but doesn't prove they committed the crime, results take much longer than TV shows, and analysis of old evidence is reversing some sentences34
1163618302cloning organisms may lead to production ofstem cells fro reseach and other applications35
1163618303in animal cloning, the nucleus of an egg isremoved and replaced with the diploid nucleus of a body cell, a process termed nuclear transplantation36
1163618304the ability of a body cell to successfully form a clonedecreases with embryotic development and cell differentiation37
1163618305the major goal of most animal cloning isreproduction, but not for humans38
1163618306in humans, the major goal is the production ofstem cells39
1163618307a stem cell can bothreproduce itself indefinitely and, under the proper conditions, produce other specialized cells; stem cells have enormous potential for medical applications40
1163618308the practical applications of DNA technology affect our lives in6 ways41
11636183091.Diagnosis of disease: if the sequence of a particular virus' DNA or RNA is known, PCR can be used toamplify patient's blood samples to detect even small traces of the virus42
1163618310different alleles have different DNAsequences43
1163618311these different sequences can be found usingrestiction enzymes that yield different lengths of DNA fragments or restriction fragment length polymorphisms (RFLP)44
1163618312The difference in banding patterns after electrophoresis allows for diagnosis of thedisease, or even a carrier of the disease45
11636183132. Gene therapy: the alteration of an afflicted individual'sgenes; gene therapy holds a great potential for treating disorders traceable to a single, defective gene, such as cystic fibrosis46
11636183143. the production of pharmaceuticals:gene splicing and cloning can be used to produce large amounts of particular proteins in the lab47
11667703664. forensic applicationsDNA samples taken from the blood, skin cells, or hair of alleged criminal suspects can be amplified with PCR and compared to DNA collected from the crime scene. DNA fingerprints (electrophorotic bands that are unique to each individual) can be compared and used to identify people at the crime scene48
11667703675. environmental cleanupscientists engineer metabolic capabilities into microorganisms, which are then used to treat environmental problems such as removing heavy metals from toxic mining sites, or engineering bacteria to digest oil49
11667703686. Agricultural applicationscertain genes that produce desirable traits have been inserted into crop plants to increase their productivity and efficiency, we have genetically engineered rice to contain vitamin A, saving about 60,000 children in Asia per year from death due to this deficiency50
1166770369An organism that has acquired by artificial means one or more genes from another species or variety is termed agenetically modified organism (GMO)51

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