20 +11 Flashcards

1
Q

What is the polymerase chain reaction (PCR)?

A

It amplifies a gene by copying it over and over again.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are the three basic steps in PCR?

A

Denaturation, Annealing, extension

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is DNA sequencing?

A

Figuring out the order of the nucleotides in a gene.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

How are restriction enzymes like transcription factors? How are they different?

A

They are like transcription factors because they are used to regulate cell processes. They are different because the transcription factors are located on the DNA strands and the restriction enzymes aren’t attached.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

How could reverse transcriptase be used to produce clones of genes without introns?

A

Reverse transcriptase transcribes the DNA backwards so that the cDNA can find its complementary intron.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Why would a researcher want clones of genes without introns?

A

This would be beneficial if they want to study only the sequences that are leaving the cell.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What does reverse transcriptase do?

A

It transcribed DNA into mRNA backwards.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

How could reverse transcriptase be used to reveal which genes in a cell’s genome were expressed at a given time?

A

It could be used with cDNA to remove the introns. Only the exons would be left and these are the sequences that are expressed.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

How can in vitro mutagenesis be used to study the function of a gene in an organism? How does this create a “knock out” organism?

A

It can be used by introducing a mutation into a cloned gene and then inserting that gene into a cell. It disables the other copies of that gene in the cell.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

How can RNA interference be used to study the function of a gene in an organism?

A

Synthetic RNA can be used to mimic the processes in which the cell uses interfering RNA to degrade mRNA or stop translation.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is a SNP?

A

An SNP is called single nucleotide polymorphism. It is when 1% of the population has a base pair variation at one site.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Describe three applications of PCR.

A

forensic analysis
ecological study
copy genes for genetic engineering
evolution study

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Describe three applications of DNA sequencing.

A

understanding genetics-phenotype
medical (disease origin/risk, understanding cell physiology, personalized medicine)
understanding development
evolutionary relationships

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is meant by “cloning a gene”?

A

Cloning a gene makes a copy of a specific gene.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is the utility of cloning a human gene into a plasmid?

A

Plasmids replicate independently, so this would allow the gene to clone faster.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is meant by “cloning an organism”?

A

Cloning an organism inserts its DNA into an embryo so that it will have the same phenotype and genotype as
the cloned organism.

17
Q

What is the utility of coning an organism?

A

The purpose is to create genetically identical organisms.

18
Q

What sort of organisms produce restriction enzymes and what is their function?

A

Bacteria and archaea produce restriction enzymes and they cut DNA at specific points on the sequence.

19
Q

How are restriction enzymes used when conducting gene splicing?

A

They can cut out unwanted sequences from the DNA so that only certain parts are used for the experiment.

20
Q

How are restriction enzymes selected to create “sticky ends” when a gene is moved from its normal chromosome, into the chromosome of another organism?

A

Sticky ends are the single stranded ends created by restriction enzymes. They can bond with the complementary sticky end of a strand in another chromosome.

21
Q

Even though the SNP shown in figure 20.14 is not part of the gene being studied, how does checking for it. Does a person still tend to indicate if that individual is carrying the normal or diseased gene?

A

If the person has the SNP, then they are unlikely to have the disease gene.

22
Q

What are pluripotent stem cells and why are they special?

A

They are able to develop into many different cell types

23
Q

What is unique about totipotent stem cells?

A

The cells can generate a complete new organism

24
Q

How does the ability to convert adult pluripotent stem cells into totipotent stem cells avoid controversy?

A

avoid taking cells from the embryo

25
Q

What is controversial about human gene therapy?

A

Unnatural, unknown side effects, against some people’s beliefs

26
Q

How is “CRISPR” better for cutting DNA than restriction enzymes like EcoR1?

A

It can be more specific than restriction enzymes

27
Q

Why are gap junctions and plasmodesmata needed for cell to cell communication if cells are adjacent to one another?

A

They both provide a pathway through the cell membrane.

28
Q

How is synaptic signaling more precise than signaling through gap junctions/plasmodesmata?

A

Synaptic signaling uses neurotransmitters to act as a chemical signal. This allows only the target cell to accept the signal. Cap junctions and plasmodesmata are only holes in which cellular contents can pass. Unwanted materials might also pass through when this method is used

29
Q

How is paracrine signaling different from endocrine signaling?

A

Paracrine signaling is an example of local signaling and endocrine signaling is long-distance signaling.

30
Q

Why do G protein coupled receptors need to have both hydrophobic and hydrophilic regions?

A

This is because they are integral proteins that reside in the cytoplasm but need a hydrophobic region so that they can attach to the cell membrane.

31
Q

How can a receptor protein function if it is located inside a cell (vs in the plasma membrane)?

A

It floats around until a hormone attaches to it. It then enters the nucleus to active/deactivate certain genes.

32
Q

How can the transduction of a signal through a cell in many steps lead to the signal becoming much stronger (amplified)?

A

This is because more enzymes each time.

33
Q

How is it that a hormone distributed through the bloodstream to the whole body alters the activity of certain cells, but has no effect on other cells?

A

Not all cells have the receptor for that hormone.

34
Q

How is it that a hormone distributed through the bloodstream can have opposite effects on different cell types? (Ex. epinephrine increases the activity of skeletal muscle but decreases the activity of smooth muscle).

A

The receptor protein may be complementary to different genes so that different responses can occur.

35
Q

Towards which charge does DNA migrate during electrophoresis?

A

It migrates towards the positive charge.

36
Q

Which part of each nucleotide is electrically charged?

A

The phosphate groups are negatively charged.

37
Q

What variables determine how far a band moves in the gel?

A

The size of the DNA fragments and how much charge it has.

38
Q

How can a segment of interest be detected on a pcr gel with many bands? (CATCATCATCATCATCATCATCATCATCAT)

A

If the DNA probe contains the complementary sequence (GTAGTAGTAGTAGTAGTAGTAGTAGTAGTA) it will attach to the DNA.

39
Q

If you put one drop of saliva into a DNA loading well, you would not have enough DNA to get identifiable bands. How could you get enough DNA from a drop of saliva in order to detect sequences of interest in DNA?

A

You could perform PCR on the DNA to amplify it.