DNA Replication and Repair

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MCAT Biology › DNA Replication and Repair

Questions 1 - 10
1

A culture of human tissue is being grown in a lab to study mitosis. A solution containing radioactively labelled cytosines was added to the culture in the middle of prophase, and then growth was halted at the end of telophase. Where would the scientists see radioactively labelled DNA?

No where

In the nuclei of every cell

Only in the nuclei of half of the cells

In the cells produced at the end of telophase—only the daughter cells

In the mother cells only—not in the cells produced at the end of telophase

Explanation

DNA is replicated in S phase. Prophase is a part of mitosis, or M phase. Since all of the DNA that would be present at the end of telophase had already been synthesized in S phase, none of the radioactively labelled cytosines would be incorporated into the DNA of any cells in the culture.

2

Which answer choice correctly matches the molecule with its function in DNA replication?

Topoisomerase—untangles supercoils

Single-stranded binding proteins—prevents reannealing of DNA during replication

Topoisomerase—prevents reannealing of DNA during replication

Single-stranded binding proteins—untangles supercoils

Polymerase—adds nucleotides to new strands

Primase—unzips DNA

Polymerase—adds RNA primers prior to replication

Primase—adds nucleotides to new strands

DNase—adds nucleotides to new strands

Single-stranded binding proteins—untangles supercoils

Explanation

Topoisomerase functions to untangle the supercoiling of DNA, which is when DNA overwinds into itself. This mechanism facilitates the unwinding action of helicase during replication. Single-stranded binding proteins bind to the two unzipped DNA strands to prevent them from prematurely coming back together into a whole molecule; otherwise replication would be interrupted.

The other proteins discussed serve the following functions.

Polymerase—adds nucleotides to new strands

Primase—adds RNA primers prior to replication

DNase—cleaves and degrades DNA molecules

3

Which base pair requires the most amount of energy to break?

G-C

A-T

G-T

T-C

T-G

Explanation

The guanine and cytosine base pairing forms 3 hydrogen bonds. Both adenine and thymine form only 2 hydrogen bonds. Thus the G-C base pair has the strongest interactions, and requires the most amount of energy to break.

4

Which base pair requires the least amount of energy to break?

A-T

G-C

G-T

T-C

T-G

Explanation

The adenine and thymine base pairing forms 2 hydrogen bonds. Both cytosine and guanine form three hydrogen bonds. Thus the A-T base pair has the weakest interaction, and requires the least amount of energy to break.

5

The central nervous system consists of the brain and the spinal cord. In general, tracts allow for the brain to communicate up and down with the spinal cord. The commissures allow for the two hemispheres of the brain to communicate with each other. One of the most important commissures is the corpus callosum. The association fibers allow for the anterior regions of the brain to communicate with the posterior regions. One of the evolved routes from the spinal cord to the brain is via the dorsal column pathway. This route allows for fine touch, vibration, proprioception and 2 points discrimination. This pathway is much faster than the pain route. From the lower limbs, the signal ascends to the brain via a region called the gracile fasciculus. From the upper limbs, the signal ascends via the cuneate fasciculus region in the spinal cord.

The dorsal column pathway is a fast and advanced signaling system. Some researchers believe that this pathway evolved not to long ago. If this transformation required the change in the DNA, how might this have occurred?

I. Point mutation

II. Frame shift

III. Nonsense mutation

I, II, and III

I only

II only

III only

I and II

Explanation

All of these choices may cause a change in the DNA. A point mutation involves a single base pair change in the DNA or the RNA. A frameshift mutation involves a deletion or insertion, in which any number of base pairs are inserted or deleted, which causes a shift in the reading frame of the DNA (not RNA). A nonsense mutation involves the change in DNA that results in a premature stop codon in the mRNA.

6

Several enzymes are required for DNA replication. What is the class of enzymes that is required for unwinding the DNA at the replication fork?

DNA helicase

DNA polymerase

Topoisomerase

Telomerase

Explanation

DNA helicases use ATP to break the hydrogen bonds that separate complementary strands of DNA. During DNA replication, DNA helicases move along the DNA backbone with the replication fork and are responsble for unwinding the DNA at the fork.

7

Compared to RNA polymerase, DNA polymerase has a much lower error rate for nucleotide incorporation. What structural difference between the two polymerases accounts for this?

DNA polymerase contains a proof-reading domain that allows it to recognize incorrect base-pair insertion before moving on; RNA polymerase does not.

RNA molecules are proofread after they are synthesized, whereas DNA molecules are not.

RNA is much less stable that DNA, and this instability makes it much harder for RNA polymerase to proofread as it incorporates bases into the sequence.

RNA polymerase incorporates the nucleic acids into sequences in such a way that they are more tightly bound to their partner nucleic acid, thus making it much more difficult to replace incorrect insertions.

Explanation

RNA polymerase does not contain a proof reading domain, making it much more error prone than DNA polymerase. This domain in DNA polymerase prevents incorrect nucleotide insertion, reducing the errors made in DNA replication.

8

Which of the following choices represents the structure of DNA from least organized to most organized?

Deoxyribose, nucleoside, nucleotide, DNA double helix, nucleosome, chromatin

Deoxyribose, nucleoside, nucleotide, DNA double helix, chromatin, nucleosome

Nucleotide, deoxyribose, nucleotide, DNA double helix, chromatin, nucleosome

Deoxyribose, nucleoside, chromatin, DNA double helix, nucleotide, nucleosome

None of these

Explanation

Deoxyribose is the sugar in the backbone of DNA. Next, a nitrogenous base is attached to the deoxyribose, which together, is called a nucleoside. A nucleoside with one or more phosphate groups attached is called a nucleotide. The double stranded DNA coils around histone proteins; this complex is called a nucleosome. Lastly the DNA gets further packaged and condensed into chromatin.

9

Which of the following is the first to act during DNA replication?

Helicase

DNA polymerase

Primase

DNA ligase

Explanation

Helicase is the first component of the DNA replication machinery to act during replication. It works by "unzipping" the double-stranded DNA so that replication can subsequently occur. Following the work of helicase, primase creates a primer to which the DNA polymerase will subsequently add deoxynucleotides and elongate the strand. DNA ligase acts at the end of replication by joining together the Okazaki fragments of the lagging strand.

10

Prions are the suspected cause of a wide variety of neurodegenerative diseases in mammals. According to prevailing theory, prions are infectious particles made only of protein and found in high concentrations in the brains of infected animals. All mammals produce normal prion protein, PrPC, a transmembrane protein whose function remains unclear.

Infectious prions, PrPRes, induce conformational changes in the existing PrPC proteins according to the following reaction:

PrPC + PrPRes → PrPRes + PrPRes

The PrPRes is then suspected to accumulate in the nervous tissue of infected patients and cause disease. This model of transmission generates replicated proteins, but does so bypassing the standard model of the central dogma of molecular biology. Transcription and translation apparently do not play a role in this replication process.

This theory is a major departure from previously established biological dogma. A scientist decides to test the protein-only theory of prion propagation. He establishes his experiment as follows:

Homogenized brain matter of infected rabbits is injected into the brains of healthy rabbits, as per the following table:

Rabbit 1 and 2: injected with normal saline on days 1 and 2

The above trials serve as controls.

Rabbit 3 and 4: injected with homogenized brain matter on days 1 and 2

The above trials use unmodified brain matter.

Rabbit 5 and 6: injected with irradiated homogenized brain matter on days 1 and 2

The above trials use brain matter that has been irradiated to destroy nucleic acids in the homogenate.

Rabbit 7 and 8: injected with protein-free centrifuged homogenized brain matter on days 1 and 2

The above trials use brain matter that has been centrifuged to generate a protein-free homogenate and a protein-rich homogenate based on molecular weight.

Rabbit 9 and 10: injected with boiled homogenized brain matter on days 1 and 2

The above trials use brain matter that have been boiled to destroy any bacterial contaminants in the homogenate.

In the material used with Rabbits 5 and 6, irradiation was used to destroy DNA. In functioning, normal cells, what types of genes typically code for DNA repair proteins?

I. Tumor suppresor genes

II. Proto-onco genes

III. Pro-apoptotic genes

I, only

I and II, only

I, II, and III

I and III, only

II and III, only

Explanation

Tumor suppresor genes, like p53 and Rb, usually code for DNA repair enzymes. Proto-oncogenes typically code for cell growth factors or receptors, and pro-apoptotic proteins would not lead to DNA repair, but would prevent tumor development via cell death pathways.

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