20.1 – 1 look at the illustration of “cloning a human gene in a bacterial plasmid” (figure...

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20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells in step 5 did not contain ampicillin, cells containing no plasmid would be allowed to grow into colonies. What color would those colonies be, and why?

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Page 1: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.1 – 1Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells in step 5 did not contain ampicillin, cells containing no plasmid would be allowed to grow into colonies. What color would those colonies be, and why?

Page 2: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

Cloning a human gene in a bacterial plasmid

Page 3: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

Cloning a human gene in a bacterial plasmid

Bacterial cell

Human cell

Page 4: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

Isolate DNA

Bacterial plasmid

Human chromosomes

lacZ gene

ampr gene

Page 5: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

Restriction enzymes

Bacterial plasmid

gene of interest

ampr gene

broken

lacZ

gene

Page 6: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

Mix together

Page 7: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

Mix together

Page 8: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

Add bacteria

Page 9: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

Add bacteria

Page 10: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

Grow on ampicillin

Page 11: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

Grow on ampicillin

Page 12: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

Add lactose mimic

Page 13: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

Add lactose mimic

Page 14: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.1 – 1Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells in step 5 did not contain ampicillin, cells containing no plasmid would be allowed to grow into colonies. What color would those colonies be, and why?

Page 15: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.1 – 1White (No functional lacZ gene is present.)

Page 16: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.1 – 2Imagine you want to study human β-globin, a protein found in red blood cells. To obtain sufficient amounts of the protein, you decide to clone the β-globin gene. Would you construct a genomic library or a cDNA library? What material would you use as a source of DNA or RNA?

Page 17: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.1 – 2A cDNA library, made using mRNA from developing red blood cells, which would be expected to contain many copies of β-globin mRNA’s.

Page 18: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.1 – 3What are two potential difficulties in using plasmid vectors of human proteins from cloned genes?

Page 19: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.1 – 3Some human genes are too large to be incorporated into bacterial plasmids. Bacterial cells lack the means to process RNA transcripts, and even if the need for RNA processing is avoided by using cDNA, bacteria lack enzymes to catalyze the post-translational processing that many human proteins undergo.

Page 20: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.2 – 1Suppose you carry out electrophoresis on a sample of genomic DNA isolated from an individual and treated with a restriction enzyme. After staining the gel with a DNA-binding dye, what would you see? Explain.

Page 21: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.2 – 1Any restriction enzyme will cut DNA in many places, generating such a large number of fragments that they would appear as a smear rather than distinct bands when the gel is stained after electrophoresis.

Page 22: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.2 – 2Explain why restriction fragment length polymorphisms (RFLPs) can serve as genetic markers even though they produce no visible phenotypic differences.

Page 23: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.2 – 2RFLPs are inherited in a Mendelian fashion, and variations in RFLPs among individuals can be detected by Southern blotting.

Page 24: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.3 – 1What is a major difference between a genetic (linkage) map and a physical map of a chromosome?

Page 25: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.3 – 1In a genetic linkage map, genes and other markers are ordered with respect to each other, but only the relative distances between them are known. In a physical map, the actual distances between markers, expressed in base pairs, are known.

Page 26: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.3 – 2In general, how does the approach to genome mapping used in the Human Genomic Project differ from the shotgun approach?

Page 27: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.3 – 2The three-stage approach employed in the Human Genome Project involves genetic mapping, physical mapping, and then sequencing of short, overlapping fragments that previously have been ordered relative to each other.

continued…

Page 28: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.3 – 2The shotgun approach eliminates the genetic mapping and physical mapping stages; instead, short fragments generated by multiple restriction enzymes are sequenced and then subsequently ordered by computer programs that identify overlapping regions.

Page 29: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.4 – 1Current estimates are that the human genome contains about 25,000 genes, but there is evidence for many more different polypeptides. What process might explain this discrepancy?

Page 30: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.4 – 1Alternative splicing of RNA transcripts from a gene and post-translational processing of polypeptides.

Page 31: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.4 – 2What is the major value of DNA microarray analysis for studying gene expression?

Page 32: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.4 – 2It allows the expression of thousands of genes to be expressed simultaneously, thus providing a genome-wide view of which genes are expressed in different tissues, under particular conditions, or at different stages of development.

Page 33: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.4 – 3Why is the genetic variation among people so much less than it is among individuals of many other species?

Page 34: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.4 – 3Because the human species arose more recently than many other species, there has been less time for genetic variations in coding and noncoding DNA to accumulate.

Page 35: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.5 – 1What is the advantage of using stem cells for gene therapy?

Page 36: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.5 – 1Stem cells continue to reproduce themselves.

Page 37: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.5 – 2List at least three different properties that have been acquired by crop plants via genetic engineering.

Page 38: 20.1 – 1 Look at the illustration of “Cloning a Human Gene in a Bacterial Plasmid” (Figure 20.4 in the orange book). If the medium used for plating cells

20.5 – 2•Herbicide resistance•Pest resistance•Disease resistance•Delayed ripening•Improved nutritional value