BIOL 3113 Lecture Notes - Lecture 11: Gene Duplication, Transfer Dna, Dna Replication

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skyoyster943

13 May 2020

School

University of Oklahoma

Department

BIOL

Course

BIOL 3113

Professor

Barbara S

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Document Summary

Although a stable genome is essential for the existence of both the individual and the species, the origin of the differences between individuals and the origin of species depends on the ability of the genome to undergo change. Genetic changes that offer an organism a selective advantage are the most likely to be preserved. *mutation within a gene - point mutations: change a single nucleotide, duplicate or delete one or more nucleotides in gene dna sequence, usually a results of rare mistakes made during dna replication or failures in dna repair after dna damage. *gene duplication: existing gene, its part or large segment of dna can be duplicated, it creates a set of closely related genes in a single cell. After additional mutations in cell progeny, duplicated genes can assume functions distinct from those of the original gene. Source of genetic novelty for evolving organisms: duplications of oncogenes- common cause of many cancers.

Related Questions

Cystic fibrosis is caused by mutations in the CFTR gene, whichencodes for a chloride channel. You are studying cystic fibrosispatients to determine what mutation they possess in the CFTR gene.The difference between the mutant and wild type CFTR genes can beuncovered by examining the CFTR:

(1 point - partial possible)

DNA

mRNA

protein

You decide to identify the CFTR mutation by analyzing thegenomic DNA of your patients compared to genomic DNA of healthyindividuals. You specifically are looking to see whether a specificgene truncation has occurred in the patients. You will determinethis using hybridization techniques. Which of the following willallow you to accomplish this?

(1 point - partial possible)

Using an RNA probe complementary to the region not removed bythe truncation.

Using an RNA probe complementary to the region removed by thetruncation.

Using an DNA probe complementary to the region not removed bythe truncation.

Using an DNA probe complementary to the region removed by thetruncation.

You would like to ensure that this experiment (to determinewhether patients have a specific CFTR gen truncation usinghybridization) is properly controlled. Which of the followingsamples must you include?

(1 point - partial possible)

The genome of a healthy individual who does not have CFTR.

The genome of a CFTR patient known to have the specifictruncation you are trying to identify.

The genome of a CFTR patient with a point mutation in a separateregion of the gene but without the disease truncation.

The genome of a healthy individual married to a CFTR patientwith the specific truncation you are trying to identify.

The genome of a patient with muscular dystrophy, which can bedue to a trucation in the dystrophin gene.

To conduct the hybridization experiment, you are trying todecide between using a DNA or RNA probe. Which would be a betterchoice and why?

(1 point)

An RNA probe because RNA has uracil bases.

An RNA probe because it could also be used in a translationexperiment.

A DNA probe because it is more stable than RNA.

A DNA probe because RNA cannot bind to DNA.

Which of the following will lower the Tm of a given DNAstrand?

(1 point - partial possible)

Increasing the percentage of GC base pairs.

Raising the pH of the solution from extremely acidic toneutral.

Decreasing the salt concentration in the DNA solution from 50mMNaCl to 5mM NaCl.

None of the above.

Imagine Hershey/Chase had used an RNA virus (genome composed ofRNA) instead of a DNA virus in their experiment. Wouldradioactivity still have been found in the pellet?

(1 point)

A.No, because only DNA can be labeled with radioactivity.

B.No, because the RNA genome would not enter the bacteria uponinfection.

C. No, because while DNA and RNA nucleotides are similar, theyare not identical.

D. Yes, because DNA and RNA nucleotides are similar.

Griffith and Avery's transformation experiments allowed us toidentify that DNA is our genetic information. Which of thefollowing scenarios would result in bacterial cells that arecapable of killing mice upon injection?

(1 point - partial possible)

A. Heat killed non-virulent bacteria is added to a live virulentbacteria strain.

B. Heat killed virulent bacteria is added to a heat killednon-virulent bacteria strain.

C. A heat killed virulent bacteria that is treated with anuclease, is then added to a non-virulent bacteria strain.

D.Heat killed mouse cells are added to a non-virulentbacteria.

The human genome consists mostly of non-coding DNA. Which of thefollowing are benefits of this?

(1 point - partial possible)

A. Random DNA mutations generally won't affect RNA and proteinfunction.

B. It is faster to duplicate the genome when these arepresent.

C. The existence of introns can lead to multiple variations ofproteins encoded by a single gene.

D. Abundant non-coding genome is a protective feature againstthe consequences of transposition of mobile elements.

bronzewater-buffalo862

Question 1

1 pts

Cystic fibrosis is caused by nonsense and missense mutations in the CFTR gene, which encodes for a chloride channel. You are studying cystic fibrosis patients to determine what mutation they possess in the CFTR gene. The difference between the mutant and wild type CFTR genes can be uncovered by examining the CFTR:

	DNA
	mRNA
	protein
	tRNA

Question 2

1 pts

You decide to identify the CFTR mutation by analyzing the genomic DNA of your patients compared to healthy individuals. You specifically are looking to see whether a specific 3' gene truncation has occurred in the patients. You will determine this using hybridization techniques with samples from healthy and CF patients. Which of the following will allow you to accomplish this?

	Using an RNA probe complementary to the region not removed by the truncation.
	Using an RNA probe complementary to the region removed by the truncation.
	Using an DNA probe complementary to the region not removed by the truncation.
	Using an DNA probe complementary to the region removed by the truncation.

Question 3

1 pts

You would like to ensure that this experiment (to determine whether patients have a specific CFTR gene truncation using hybridization) is properly controlled. Which of the following samples must you test?

	The genomic DNA of a healthy individual who does not have cystic fibrosis.
	The genome of a CFTR patient known to have the specific truncation you are trying to identify.
	The genome of a CFTR patient with a missense mutation but full length gene.
	The genome of a healthy individual married to a CFTR patient with the specific truncation you are trying to identify.
	The genome of a patient with muscular dystrophy, which can be due to a trucation in the dystrophin gene.

Question 4

1 pts

To conduct the hybridization experiment, you are trying to decide between using a DNA or RNA probe. Which would be ideal to use and why?

	As both are composed of nucleic acids, using either would result in identical results.
	An RNA probe because RNA has uracil bases.
	An RNA probe because it could also be used in a translation experiment.
	A DNA probe because it is more stable than RNA.
	A DNA probe because RNA cannot bind to DNA.

Question 5

1 pts

Which of the following will lower the Tm of a given DNA strand?

	Increasing the percentage of GC base pairs.
	Raising the pH of the solution from neutral to basic.
	Decreasing the buffer concentration from 50mM NaCl to 5mM NaCl.
	None of the above.

Question 6

1 pts

One step of the Hershey/Chase experiment involved blending the virus/cell mixture before centrifugation and probing the pellet for radioactivity. Why was the blending step necessary?

	To collect the bacteria at the bottom of the tube.
	To break open the bacteria to release the genome.
	To separate the bacteria from the bacteriophages.
	To be able to detect the radioactivity.

Question 7

1 pts

Imagine Hershey/Chase had used an RNA virus (genome composed of RNA) instead of a DNA virus in their experiment. Would radioactivity still have been found in the pellet?

	No, because only DNA can be labeled with radioactivity.
	No, because the RNA genome would not enter the bacteria upon infection.
	No, because while DNA and RNA nucleotides are similar, they are not identical.
	Yes, because DNA and RNA nucleotides are similar.
	Yes, because genome in any form (DNA, RNA, protein) would be labeled similarly.

Question 8

1 pts

Griffith and Avery's transformation experiments allowed us to identify that DNA is our genetic information. Which of the following scenarios would result in bacterial cells that are capable of killing mice upon injection?

	Heat killed non-virulent bacteria is added to a live virulent bacteria strain.
	Heat killed virulent bacteria is added to a heat killed non-virulent bacteria strain.
	A heat killed virulent bacteria that is treated with a nuclease, is then added to a non-virulent bacteria strain.
	Heat killed mouse cells are added to a non-virulent bacteria.

Question 9

1 pts

The human genome consists mostly of non-coding DNA. Which of the following are benefits of this?

	Random DNA mutations generally won't affect RNA and protein function.
	It is faster to duplicate the genome when these are present.
	The existence of introns can lead to multiple variations of proteins encoded by a single gene.
	It is unlikely transposons would exist in the genome if there was too much protein coding DNA.

Question 10

1 pts

Andrew Murray's sister, Andrea, is adding to her brother's work on chromosomes. She is using cells that are unable to synthesize adenine (âade) and histidine (âhis). The plasmid she is currently working with consists of an origin of replication and the Ade gene.

Following her transformation of the plasmid into her yeast, what media will the cells be plated on to select for cells that have picked up the plasmid?

	Media containing histidine
	Media containing adenine
	Media lacking adenine
	Media lacking histidine

tealcockroach755

	Using an RNA probe complementary to the region not removed by the truncation.
	Using an RNA probe complementary to the region removed by the truncation.
	Using an DNA probe complementary to the region not removed by the truncation.
	Using an DNA probe complementary to the region removed by the truncation.

To conduct the hybridization experiment, you are trying to decide between using a DNA or RNA probe. Which would be ideal to use and why?

	As both are composed of nucleic acids, using either would result in identical results.
	An RNA probe because RNA has uracil bases.
	An RNA probe because it could also be used in a translation experiment.
	A DNA probe because it is more stable than RNA.
	A DNA probe because RNA cannot bind to DNA.

Imagine Hershey/Chase had used an RNA virus (genome composed of RNA) instead of a DNA virus in their experiment. Would radioactivity still have been found in the pellet?

	No, because only DNA can be labeled with radioactivity.
	No, because the RNA genome would not enter the bacteria upon infection.
	No, because while DNA and RNA nucleotides are similar, they are not identical.
	Yes, because DNA and RNA nucleotides are similar.
	Yes, because genome in any form (DNA, RNA, protein) would be labeled similarly.

The human genome consists mostly of non-coding DNA. Which of the following are benefits of this?

	Random DNA mutations generally won't affect RNA and protein function.
	It is faster to duplicate the genome when these are present.
	The existence of introns can lead to multiple variations of proteins encoded by a single gene.
	It is unlikely transposons would exist in the genome if there was too much protein coding DNA.

You accidentally add a mutant dNTP (which has an H instead of an OH connected to the 3â carbon) to a reaction where DNA is being replicated. Which of the following is true of this mutant dNTP?

	It can be incorporated into DNA strand but cannot form a phosphodiester bond with an incoming wild type dNTP
	It can be incorporated into a DNA strand but cannot base pair with a complementary nucleotide
	It can be incorporated into a DNA strand and can form a phosphodiester bond with an incoming dNTP, but only if it is another mutant dNTP
	It cannot be incorporated into a DNA strand.

Following her transformation of the plasmid into her yeast, what media will the cells be plated on to select for cells that have picked up the plasmid?

	Media containing histidine
	Media containing adenine
	Media lacking adenine
	Media lacking histidine

She starts by attempting to add the centromere DNA into a plasmid containing the origin of replication. Unfortunately, when adding the centromere sequence, the origin of replication is removed, thus leaving a plasmid with only a centromere and selection marker. Following plasmid transformation, what growth result will she see on her plates?

	No colonies
	Little colonies
	Big colonies

She fixes the mistakes from the previous experiment and now has a complete plasmid (selection marker, origin of replication, centromere). She then inserts telomere sequences into the plasmid. How will this impact her transformation?

	It will not impact her transformation
	Her transformation will no longer work because plasmids donât require telomeres
	She will now see much larger colonies
	She will now see fewer but larger colonies
	She will now see smaller colonies

In the Meselson/Stahl experiment, E. coli were first grown in media containing heavy nitrogen, 15N, and then transferred to light nitrogen, 14N, at the beginning of the experiment.

Imagine that their data showed that replication occurs in a conservative manner instead of semi-conservative. What fraction of the DNA helices will consist of mixed DNA after 4 rounds of replication in this case?

	None
	More than 75%
	25-50%
	51-75%
	Less than 25%

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BIOL 3113 Lecture Notes - Lecture 11: Gene Duplication, Transfer Dna, Dna Replication

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