Question

In: Biology

Pick the correcty answer If a mutation that inactivated telomerase occurred in a cell (telomerase activity...

Pick the correcty answer

If a mutation that inactivated telomerase occurred in a cell (telomerase activity in the cell = zero), what do you expect the outcome to be?

The position of the centromere would shift at each replication cycle, eventually leading to mutations in the genetic information and cell death.
The number of tandem repeats would increase with each replication cycle, eventually leading to a large unstable chromosome and cell death.
The telomeres would shorten at each replication cycle, eventually leading to loss of essential genetic information and cell death.
DNA primase would be unable to bind to the 5 end of the template strand, eventually causing a reduction in chromosome size and cell death.

Somatic or body cells have very little telomerase. As a result, the telomeres within these (proliferating) cells _____ with each cell division.

shorten
lengthen
remain constant in size
can either shorten or lengthen
None of the answers is correct.

A researcher is studying telomerase in four types of mouse cells: brain cells, skin cells, blood cells, and gametes (sperm/eggs). What do you suspect she will find?

telomerase activity/amount will be highest in skin cells
telomerase activity/amount will be highest in brain cells
telomerase activity/amount will be highest in blood cells
telomerase activity/amount will be highest in gametes (sperm/eggs)
telomerase activity/amount will be the same in all of the cell types
Examples of hybridization of single-stranded DNAs used in Chapter 10 include:
primers used in DNA sequencing and in PCR
sticky-end cloning
probes used in Southern and Northern blotting and in diagnosis of mutations
All of the answer options are correct.
Examples of proteins that bind to DNA and then act on it, found in Chapter 10, include:
restriction enzymes
Taq DNA polymerase
DNA ligase
All of the answer options are correct.
Why is ligase needed to make recombinant DNA?
It enables the donor fragments and the vector DNA molecules to initially hybridize.
It is responsible for forming the complementary sticky ends of the donor fragments and the vector DNA.
It is only used when blunt-ended vectors are used to form recombinant plasmids.
It creates phosphodiester bonds at the sites where inserted DNA and vector have attached by complementary base pairing.
It is used in the isolation of recombinant plasmids from those plasmid vectors that did not take up donor DNA.
What would be the immediate consequence in the cloning process if someone forgot to add ligase?
There would be no hybridization between the vectors and the donor DNA fragments.
No complementary sticky ends would form in either the vectors or the donor DNA molecules.
Blunt-ended vectors would be able to form covalent bonds with donor DNA.
The inserted DNA and the vector would be held together only by hydrogen bonds, so recombinant plasmids would lose the inserted DNA.
Recombinant plasmids could not be separated from nonrecombinant plasmids.

In the PCR process, if we assume that each cycle takes five minutes, how many-fold amplifications would be accomplished in one hour?

12-fold
32-fold
512-fold
4096-fold
The position of the gene for the protein actin in the haploid fungus Neurospora is known from the complete genome sequence. If you had a slow-growing strain that you suspected of being an actin mutant and you wanted to verify that it was one, would you (1) clone the mutant by using convenient restriction sites flanking the actin gene and then sequence it, or (2) amplify the mutant sequence by using PCR and then sequence it?
The better choice is to clone and sequence the actin gene to confirm that it has mutated. This is a dependable method provided that suitable restriction sites are available.
The better choice is to amplify the actin gene sequence from the mutant and sequence it to confirm that it has mutated. PCR requires fewer steps, and it can be completed more quickly. However, it requires the production of suitable primers.
Why is it necessary to use a special DNA polymerase (Taq polymerase) in PCR?
because the reaction starts with very small amounts of DNA template
because the polymerase has to be able to remain active after heating to 95 degrees Celsius
because the reaction uses primers which are not usually required for DNA replication
because the amount of template increases with each cycle

One feature that virtually all plasmid vectors have in common is the polylinker (also called a multiple cloning site). This is important because

it helps select transformants from nontransformants.
it carries convenient restriction enzyme sites into which the DNA to be cloned may be inserted.
it allows the vector to replicate independent of host.
All of the answer options are correct.
Virtually all plasmid vectors have a selectable marker. This is important because
it helps select transformants from nontransformants.
it carries convenient restriction enzyme sites into which the DNA to be cloned may be inserted.
it allows the vector to replicate independent of host.
All of the answer options are correct.
Prototrophy is often the phenotype selected to detect transformants. Prototrophic cells are used for donor DNA extraction; then this DNA is cloned and the clones are added to an auxotrophic recipient culture. Successful transformants are identified by plating the recipient culture on minimal medium and looking for colonies. What experimental design would you use to make sure that a colony that you hope is a transformant is not, in fact, a revertant (mutation back to prototrophy by a second mutation in the originally mutated gene) of the auxotrophic mutation?
Use an auxotroph that cannot revert as the recipient, such as one that contains a deletion.
Include a selectable marker on the vector that is added to the auxotrophic recipients. Then use the selection conditions to confirm that the colony is a transformant.
Sequence the gene of interest isolated from a putative transformant to determine if additional mutations have occurred.
All of the answer options are correct.

Solutions

Expert Solution

If a mutation that inactivated telomerase occurred in a cell (telomerase activity in the cell = zero), what do you expect the outcome to be?

The answer is - The telomeres would shorten at each replication cycle, eventually leading to loss of essential genetic information and cell death.

All eukaryotic chromosomes end in telomeres. The terminal that is extreme 5 prime end of each strand fails to replicate. This occurs because DNA polymerase fails to bind to this terminal ends, actually it slips. So a special enyme called telomerase is employed to catalyze the replication at telomere.

So if there is no telomerase activity then in each cycle of replication few terminal sequences would be lost eventually genetic information would be lost.

Somatic or body cells have very little telomerase. As a result, the telomeres within these (proliferating) cells _____ with each cell division.

The answer is - shorten.

A researcher is studying telomerase in four types of mouse cells: brain cells, skin cells, blood cells, and gametes (sperm/eggs). What do you suspect she will find?

The answer is - telomerase activity/amount will be highest in gametes (sperm/eggs).

In normal somatic cells telomerase activity is not observed. So they can replicate a definite number of time after that they will under go apoptosis. But germ cells that is sperm or egg shows telomerase activity.


Related Solutions

What would happen in a cell that had a mutation that inactivated the protein WASP?
What would happen in a cell that had a mutation that inactivated the protein WASP?
Whats the effect of the reeler mutation on cell-cell interaction
Whats the effect of the reeler mutation on cell-cell interaction
Tasko is an antimicrobial that interferes with telomerase activity in fungal pathogens. Explain the effects of...
Tasko is an antimicrobial that interferes with telomerase activity in fungal pathogens. Explain the effects of this drug on the yeast and why it is an effective drug.
Question 20 An example of a suppressor mutation would be A mutation that suppresses cell growth...
Question 20 An example of a suppressor mutation would be A mutation that suppresses cell growth An intergenic mutation that increases the activity of a protein performing a different function as the mutated protein An intragenic mutation that restores the inactive protein's structure An intergenic mutation that activates a transcription factor that increases the expression of a normal protein Question 23 The mechanism for reactive oxygen species to cause mutation is the reactive oxygen species stabilize different tautomeric forms of...
Which of the following cell types express telomerase to maintain their telomere lengths and extend their...
Which of the following cell types express telomerase to maintain their telomere lengths and extend their replication abilities? Select one: - somatic cells - neurons - liver cells - stem cells
Cells lacking telomerase can grow for several cell divisions without obvious defects. However, after more cell...
Cells lacking telomerase can grow for several cell divisions without obvious defects. However, after more cell divisions, such cells tend to show chromosomes that have fused together. Propose an explanation for the formation of the chromosomes.
Could you explain to me how TRAP assay works? I want to detect telomerase activity of...
Could you explain to me how TRAP assay works? I want to detect telomerase activity of breast cancer cell after the cell treated with anti-tumor (curcumin).
Explain how the sickle cell mutation results in the symptoms of the disease?
Explain how the sickle cell mutation results in the symptoms of the disease?
Why is a mutation in a signaling pathway not sufficient to create a cancer cell.
Why is a mutation in a signaling pathway not sufficient to create a cancer cell.
A accidental genetic mutation in the lab mice has occurred and affects the glycogen degradation pathway....
A accidental genetic mutation in the lab mice has occurred and affects the glycogen degradation pathway. Dr. Wilson is studying this unexpected mutation and has taken samples of their livers. What he found was excessive glycogen storage but the glycogen structure was unusual. There was a lot of glycogen but size of each glycogen molecule was smaller and each chain end had 4 glucose units (alpha 1,4 bonds) and then a SINGLE glucose attached as a branch point (alpha 1,6...
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT