Chapter 20 Flashcards

1
Q

If the medium used for plating cells in step 5 of Figure 20.4 did not contain ampicillin, cells contain- ing no plasmid would be able to grow into colonies. What color would those colonies be and why?

A

White (no functional lacZ gene is present)

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2
Q

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

A

A cDNA library, made using mRNA from developing red blood cells, which would be expected to contain many copies of ß-globin mRNAs .

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3
Q

What are two potential difficulties in using plasmid vectors and bacterial host cells for production of large quantities of human proteins from cloned genes?

A

Some 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.

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4
Q

Suppose 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.

A

Any restriction enzyme will cut genomic 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.

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5
Q

Explain why restriction fragment length polymornhisms (RFLPs) can serve as genetic markers even though they produce no visible phenotypic differences?

A

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

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6
Q

What is the major difference between a gene (linkage) map and a physical map of a chromosome?

A

In 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.

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7
Q

In general, how does the approach to genome ma - ping used in the Human Genome Project differ from the shotgun approach?

A

The 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 (see Figure 20.11). The 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 (see Figure 20.13)

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8
Q

Current estimates are that the human genome con-tains about 25,000 genes, but there is evidence for more different human polypeptides. What processes might explain this discrepancy?

A

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

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9
Q

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

A

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

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10
Q

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

A

Because 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.

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11
Q

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

A

Stem cells continue to reproduce themselves.

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12
Q

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

A

Herbicide resistance, pest resistance, disease resistance, delayed ripening, and improved nutritional value

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13
Q

Which of the following tools of recombinant DNA technology is incorrectly paired with its use?

A

DNA ligase—enzyme that cuts DNA, creating the sticky ends of restriction fragments

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14
Q

Which of the following would using human brain tissue as the starting material?

A

It could be used to create a complete genomic library.

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15
Q

Plants are more readily manipulated by genetic engineering than are animals because

A

a somatic plant cell can often give rise to a complete plant.

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16
Q

A paleontologist has recovered a bit of tissue from the 400-year-old preserved skin of an extinct dodo (a bird). The researcher would like to compare DNA from the sample with DNA from living birds. Which of the following would be most useful for increasing the amount of dodo DNA available for testing?

A

polymerase chain reaction (PCR)

17
Q

Expression of a cloned eukaryotic gene in a prokaryotic cell involves many difficulties. The use of mRNA and reverse transcriptase is part of a strategy to solve the problem of

A

post-transcriptional processing.

18
Q

DNA technology has many medical applications. Which of the following is not done routinely at present?

A

introduction of genetically engineered genes into human gametes

19
Q

Which of the following has the largest genome size and the smallest number of genes per million base pairs?

A

Homo sapiens (human)

20
Q

Which of the following sequences in double-stranded DNA is most likely to be recognized as a cutting site for a restriction enzyme?

A

a RFLP marker.

21
Q

In recombinant DNA methods, the term vector can refer to

A

a plasmid used to transfer DNA into a living eel

22
Q

When using the shotgun approach to genome mapping researchers carry out

A

DNA sequencing of small fragments and then ordering of the fragments to determine the overall nucleotide sequence.