MSA CHAPTER 12 TEST Flashcards

1
Q

Explain what recombinant DNA is

A

Recombinant DNA is formed when scientists combine nucleotide sequences for two different sources.

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2
Q

Explain gene cloning.

A
  1. plasmid is isolated
    1. cell’s DNA is isolated
    2. plasmid is cut with restriction enzyme
    3. cell’s DNA is cut with the same restriction enzyme
    4. targeted fragment/plasmid DNA is mixed
    5. DNA ligase joins the fragments of genetic material together
    6. Recombinant plasmid is taken up by bacterium in transformation
    7. Bacteria reproduces
    8. Harvested proteins may be used indirectly
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3
Q

What is a vector?

A

A vector is a gene carrier

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4
Q

Explain what DNA ligase is.

A

an enzyme that glues genetic fragments together, forms a covalent bond

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5
Q

Explain transformation.

A

Transformation is the uptaking of foreign DNA from the surrounding environment

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6
Q

What do restriction enzymes do? and where do they come from?

A

Restriction enzymes are used to cut DNA into smaller fragments. They come from bacteria

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7
Q

What are “sticky ends”?

A

Sticky ends are the ends of a DNA double helix at which unpaired nucleotides of one strand extends beyond the other.

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8
Q

Why are “sticky ends” important? What makes them sticky?

A

Sticky ends are important because they ensure that the DNA fragment is inserted in the plasmid in the right direction.

sticky ends are named “sticky” because they are able to form base pairs with any DNA molecule with the complementary sticky end

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9
Q

Explain the shotgun approach to gene cloning.

A

The shotgun approach to gene cloning is a method for determining the DNA sequence of an entire genome. After the genome is cut into small fragments, each fragment is sequenced and placed in the proper order.

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10
Q

What is a genomic library?

A

-A genomic library is the whole collection of all the cloned DNA fragments from a genome.

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11
Q

What are the ways to construct a genomic library?

A

plasmid library, bacteriophages, bacterial artificial chromosome

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12
Q

Explain what reverse transcriptase does? What is unique about the product formed?

A

everse transcriptase is an enzyme that reverses transcription. Instead of turning DNA into RNA, RNA it turned to DNA. This process happens after RNA splicing where all the introns are removed leaving behind only exons to be joined.

What is unique about this is forming cDNA or complementary DNA. cDNA is like a regular DNA molecule except that it contains no introns and only contains exons making it easier to work with than a regular DNA molecule.

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13
Q

What is cDNA? Not just the name, how is it formed? What is it composed of?

A

cDNA is a DNA molecule made from using mRNA as a template and the enzyme reverse transcriptase. It is composed like a regular DNA molecule except with no introns

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14
Q

What is a nucleic acid probe? Give two examples of how scientists can detect them.

A

A nucleic acid probe is molecule used to find a specific gene or nucleotide sequence. 1 way to find them is to putting a radioactive probes on DNA. 2nd way is to put DNA in a probe solution.

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15
Q

What does a vaccine do?
What is it composed of?

A

Vaccines stimulate the immune system to mount a lasting defense against a pathogen.

A vaccine is composed of a harmless variant or a derivative of a pathogen, such as a bacterium or a virus.
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16
Q

What is Golden Rice

What makes it gold

A

Golden rice is a transgenic variety of rice that produces yellow grains containing beta-carterone, used by our bodies to make vitamin A

The rice is gold because it was created with daffodil genes

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17
Q

What is a transgenic organism?

A

A transgenic organism is an organism that contains genes from another organism

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18
Q

What is necessary for gene therapy to be permanent for the individual person? What about for further generations?

A

In order for gene therapy to be permanent, the normal gene must be transferred to somatic cells that can continuously multiply. It can be permanent in further generations if gene therapy is used on sex cells that undergo fertilization.

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19
Q

What is DNA profiling?

A

DNA profiling is a procedure that analyzes DNA samples to determine if they come for the same individual.

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20
Q

What is PCR and what does it do?

What does amplifying DNA mean?

How does Amplifying DNA work?

A

PCR is a technique by which a specific segment of a DNA molecule can be targeted and quickly amplified.

Copying it many times.

To amplify DNA, the DNA must go through a process called PCR or polymerase chain reaction. -

21
Q

How does gel electrophoresis separate DNA fragments?

A

The DNA is negative and the electric pull of the positive end of the gel electrophoresis bring the smaller fragments towards it to separate it.

22
Q

Explain STR analysis.

A

Short Tandem Repeat analysis is the most useful method in molecular biology. The STR is a microsatellite, consisting of a unit of two to thirteen nucleotides repeated hundreds of times in a row on a DNA strand.

23
Q

Approximately what percentage of human DNA is noncoding?

A

Approximately 98% of human DNA is noncoding.

24
Q

What are transposable elements?

A

Transposable elements are sequences that can move about in the genome (jumping genes). Often times they are the cause of mutations.

25
Define proteomics.
Proteomics is the study of whole sets of proteins and their interactions.
26
Compare the number of proteins vs the number of genes in the human body.
the number of different proteins in humans far exceeds the number of genes. about 100000 proteins verses 21000 genes.
27
Gene sequencing of Neanderthals allowed scientists to say what about their physical appearance?
Males have pale skin and red hair. While as adults Neanderthals would be lactose tolerant.
28
What three different places can recombinant cell come from? Why is it necessary to use different types of cells?
Recombinant cells can be yeast, bacteria, or other cells. Bacteria are the easiest cells to use because they are not complicated. Yeast cells may be used because they are eukaryotic. In some cases other cells, for example mammalian cells, need to be used because the are as complex as the protein trying to be mass-produced.
29
Why is it a good idea to use human cells to grow human proteins?
Yes, because of you used any other kind of organisms protein in our body then our body would reject it and cause harm to us
30
What is genomics? Give examples of organisms that have had their genome mapped?
Genomics is the study of genomes and what makes them up. Mice and humans both have their genomes mapped.
31
Explain how plasmids are used in gene cloning.
Plasmids are able to carry certain genes/ gene of interest to allow for gene cloning.
32
Explain how restriction enzymes are used to “cut and paste” DNA into plasmids.
Restriction enzymes are used to “cut & paste” DNA into plasmids by recognizing specific sites. They do not cut randomly, the cut at very specific locations due to nucleotide base pair matching.
33
Explain how a cDNA library is constructed and how it is different from genomic libraries constructed using plasmids or phages.
cDNA libraries are made transcribing a second strand of DNA onto the strand made from reverse transcription. cDNA libraries are shorter than genomic libraries because cDNA only has the exons
34
Explain how a nucleic acid probe can be used to identify a specific gene.
Nucleic acid probes have a set of base pairs that is complementary with a set on the gene of interest. If the probe sticks to the gene then the specific gene had been found.
35
Explain how different organisms are used to mass-produce proteins of human interest?
Different organisms mass produce proteins of human interest through cloning. This organisms could be phages, plasmids, or BACs
36
Explain how DNA technology has helped to produce insulin, growth hormone, and vaccines.
Recombinant cells are useful to make proteins. We do this by transferring a gene into a bacterium, yeast, or other cells. Without knowing how to make recombinant cells we would not be able to make insulin, growth hormones, or vaccines, which could result in a lot of deaths that are avoidable with this technology
37
Explain how genetically modified (GM) organisms are transforming agriculture.
Genetically modified organisms are transforming agriculture by improving food production, pest resistance, and nutritional value of crops.
38
Describe the risks posed by the creation and culturing of GM organisms and the safeguards that have been developed to minimize these risks.
The risks posed by the creation and culturing of GM organisms is cancer, it may be hazardous to humans and other organisms, may lead to allergic reactions, may disease the crops easily and lead to good crops being diseased as well, and may reduce the genetic diversity. The safeguards is evaluated for potential risks, and possibly require a label.
39
Describe the benefits and risks of gene therapy in humans. Discuss the ethical issues that these techniques present.
The benefits of gene therapy are that it is can be used to treat diseases by finding an alteration of a person's gene. The risks are that it may harm other cell and can decrease genetic diversity/ the need of evolution. Ethical issues such as: How will the gene be created at the right time and place? How can it be performed without harming other cells/cell functions? Will it lead to efforts to control genetic makeup of human population, designer babies How will it affect genetic diversity/evolution?
40
Describe the basic steps of DNA profiling.
Polymerase chain reaction is a technique used in molecular biology to amplify a copy of a segment of DNA across several magnitudes.
41
Explain how gel electrophoresis is used to sort DNA and proteins.
Gel electrophoresis is used to sort DNA and proteins by separating them. DNA fragments are separated according to their size. Proteins can be separated by their size and their charge.
42
Explain how short tandem repeats are used in DNA profiling.
Short tandem repeats are favored by many forensic scientists. Short tandem repeats are short sequences that are repeated several times in different loci of someone’s DNA. Forensic scientists usually observe 10 different locis on different chromosomes to determine the relation of evidence to someone’s DNA.
43
Describe the diverse applications of DNA profiling.
DNA profiling can be used to prove people guilty or innocent. Solve questions of who’s the baby’s parent? Identify victims of accidents. Inquiry the origin of nonhuman materials
44
Explain how restriction fragment analysis is used to detect differences in DNA sequences.
Restriction length analysis is used to detect differences in DNA sequences by producing DNA fragments by restriction enzymes and sorting these fragments by gel electrophoresis.
45
Explain why it is important to sequence the genomes of humans and other organisms.
It’s important because it’s a step forward for scientists to understand how the genome works as a whole, how they work together to direct the growth, development, and maintenance of an organism as a whole.
46
Describe the structure and possible functions of the non-coding sections of the human genome.
Human DNA is comprised of abundant repeats that extend for many sections. DNA consists mostly of repetitive elements scattered with nonrepetitive sequences. These non-coding sections are responsible for coding proteins.
47
Explain how the human genome was mapped.
The human genome was mapped through an association called The Human Genome Project. It is an international program with the goal of determining the sequence of nucleotide base pairs that make up human DNA. This is how the identifying and mapping of the human genome happened.
48
Compare the fields of genomics and proteomics.
Proteomics is the study of the proteome of an organism. Proteome refers to the entire protein set coded by the genome. Genomics is the study of the genome of an organism.
49
Describe the significance of genomics to the study of evolutionary relationships and our understanding of the special characteristics of humans.
Genomics is the study of the structure of all genes and its relative position on the chromosome. It also studies the function of all genes and the role of genes in regulating metabolic activities in the cell. This idea helps us understand evolution because it gives us a simple way to compare organisms and possibly figure out if they come from a common ancestor.