MCAT DNA repair mechanisms practice questions

Practice questions on DNA repair mechanisms for MCAT preparation, covering various types of repair systems and their significance in genetics.

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What is Base Excision Repair (BER)?

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A DNA repair mechanism that corrects single-base lesions in DNA.

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1. What is Base Excision Repair (BER)?

Terms in this Study Set(64)

Base Excision Repair (BER)(16)

What is Base Excision Repair (BER)?

A DNA repair mechanism that corrects single-base lesions in DNA.

Key enzyme in BER?

DNA glycosylase: removes damaged bases.

True or False: BER can fix bulky DNA adducts.

False. BER specifically targets small base lesions.

Fill in the blank: The first step in BER involves __________.

Recognition and removal of damaged base.

What follows DNA glycosylase action in BER?

AP endonuclease cleaves the sugar-phosphate backbone.

Compare BER and NER.

BER: single base damage; NER: bulky lesions.

Cause → Effect: DNA damage caused by reactive oxygen species leads to __________.

Base mutations repaired by BER.

Which enzyme fills in the gap after base removal in BER?

DNA polymerase synthesizes the new nucleotide.

True or False: DNA ligase seals nicks in the DNA backbone during BER.

True. DNA ligase is crucial for completing the repair.

What is the role of AP endonuclease?

It creates a nick in the DNA backbone at the apurinic/apyrimidinic site.

Short Example: How does DNA glycosylase identify damaged bases?

It scans DNA and recognizes altered base structures.

Which type of damage is commonly repaired by BER?

Deamination, oxidation, and alkylation of bases.

Fill in the blank: In BER, after the gap is filled, __________ joins the ends.

DNA ligase.

List the steps in BER.

- Base removal - AP site formation - Nicking - Gap filling - Ligation

True or False: BER is error-prone and leads to mutations.

False. BER is generally accurate in correcting errors.

What is the role of DNA polymerase in BER?

It synthesizes the correct base to replace the removed one.

Nucleotide Excision Repair (NER)(16)

What is Nucleotide Excision Repair (NER)?

NER is a DNA repair mechanism that removes bulky DNA lesions, such as those caused by UV light.

List the key steps in NER.

- Damage recognition - Excision of damaged DNA - DNA synthesis - Ligation of DNA strands

True or False: NER only repairs single-strand breaks.

False. NER repairs bulky lesions and helix-distorting damage, not just single-strand breaks.

What enzyme is responsible for recognizing DNA damage in NER?

XPC protein complex recognizes damaged DNA and initiates NER.

Fill in the blank: The endonuclease that excises damaged DNA in NER is called ____.

XPF/ERCC4 and XPG/ERCC5.

Cause → Effect: What happens when NER is defective?

Increased susceptibility to UV-induced skin cancers, such as xeroderma pigmentosum.

Compare NER and Base Excision Repair (BER) processes.

NER repairs bulky lesions; BER fixes non-helix-distorting base damage.

What is the role of DNA polymerase in NER?

DNA polymerase synthesizes new DNA to fill in gaps after excision.

Name a key protein involved in the NER pathway.

XPC protein is crucial for damage recognition.

True or False: NER can fix all types of DNA damage.

False. NER is specific for bulky lesions; it cannot repair all damage types.

What happens during the 'incision' step of NER?

Endonucleases cut the DNA strand on both sides of the damaged segment.

Fill in the blank: NER is particularly important for repairing damage from _____.

UV radiation.

What is the function of the helicase in NER?

The helicase unwinds the DNA to allow access for repair enzymes.

Describe the role of ligase in NER.

Ligase seals the nicks in the DNA backbone after repair synthesis.

List two diseases associated with defective NER.

- Xeroderma pigmentosum - Cockayne syndrome

What type of damage does NER primarily address?

Helix-distorting damage such as thymine dimers.

Mismatch Repair (MMR)(16)

What is mismatch repair (MMR)?

MMR is a DNA repair mechanism that corrects base pair mismatches that occur during DNA replication.

Key enzymes involved in MMR?

- MutS: detects mismatches - MutL: links detection to repair - MutH: cleaves the daughter strand

True or False: MMR corrects DNA damage caused by environmental factors.

False. MMR specifically corrects replication errors, not damage from environmental sources.

Fill in the blank: MMR prevents the __________ of mutations during DNA replication.

accumulation

Compare MMR and NER.

MMR fixes replication errors, while NER repairs bulky DNA lesions and distortions.

What triggers the activation of MMR?

The presence of mismatched base pairs detected by MutS proteins.

Role of MutH in MMR?

MutH identifies the newly synthesized DNA strand and cleaves it to initiate repair.

What types of mismatches does MMR correct?

MMR corrects insertions, deletions, and base substitutions that lead to mismatched pairs.

True or False: MMR is essential for all organisms.

True. MMR is conserved across many species and is crucial for DNA fidelity.

What happens if MMR is defective?

Defective MMR can lead to increased mutation rates and is associated with certain cancers, such as Lynch syndrome.

Cause → Effect: MMR deficiency leads to __________.

increased microsatellite instability

What is the role of exonuclease in MMR?

Exonuclease removes the erroneous nucleotides after MutH has cleaved the strand.

Identify a key difference between MMR and Base Excision Repair.

While MMR corrects mismatched bases, Base Excision Repair fixes damaged or inappropriate bases.

Short example of MMR in action.

During DNA replication, if adenine pairs with cytosine, MutS will detect this mismatch and activate repair mechanisms.

True or False: MMR operates only in prokaryotes.

False. MMR is present in both prokaryotic and eukaryotic cells.

Name one disease associated with MMR defects.

Lynch syndrome (hereditary non-polyposis colorectal cancer).

Double-Strand Break Repair (DSBR)(16)

What is a double-strand break (DSB)?

A DSB is a type of DNA damage where both strands of the DNA helix are severed, potentially leading to genomic instability.

True or False: Non-homologous end joining (NHEJ) is error-prone.

True. NHEJ can introduce mutations because it directly ligates broken ends without template guidance.

Homologous recombination (HR) requires what type of DNA?

It requires a homologous template, usually the sister chromatid, to accurately repair the break.

Fill in the blank: NHEJ is most active during _____ phase.

G1 phase.

Comparison: NHEJ vs. HR.

- NHEJ: fast, error-prone. - HR: slower, high fidelity.

What proteins are key in NHEJ?

Key proteins include Ku70/80, DNA-PKcs, and Ligase IV.

Cause → Effect: DSBs can lead to cancer.

Unrepaired DSBs can cause chromosomal rearrangements, leading to tumorigenesis.

What role does RAD51 play in HR?

RAD51 facilitates strand invasion of the homologous template and promotes DNA pairing.

True or False: HR requires cell cycle specificity.

True. HR primarily occurs in the S and G2 phases when sister chromatids are available.

What enzymes initiate NHEJ?

Ku proteins recognize DSBs and recruit DNA-PKcs to the site.

Fill in the blank: The 5' overhangs are filled in during _____.

NHEJ process.

How does HR ensure fidelity in DNA repair?

HR uses a homologous template to guide accurate repair, reducing errors.

What happens during the exonuclease step in HR?

Exonucleases trim the ends of the broken DNA to create single-stranded overhangs for strand invasion.

Define: DNA-PKcs.

DNA-PKcs is a kinase that plays a critical role in the NHEJ pathway by phosphorylating target proteins.

What is the significance of the Holliday junction?

The Holliday junction is a key intermediate in HR, allowing for the exchange of genetic material between homologous chromosomes.

Differentiate between DSB repair pathways: NHEJ vs. HR.

- NHEJ: faster, no template. - HR: slower, uses template.

Questions in this Study Set(64)

1. What is Base Excision Repair (BER)?

A.A mechanism that corrects single-base lesions in DNA.
B.A process that repairs double-strand breaks.
C.A method for repairing bulky DNA adducts.
D.A system for fixing replication errors.

2. What occurs during a double-strand break (DSB) in DNA?

A.Both strands of the DNA helix are severed.
B.Only one strand of the DNA helix is severed.
C.DNA is completely degraded.
D.Replication of DNA stops entirely.

3. What is the primary function of mismatch repair (MMR)?

A.To correct base pair mismatches during DNA replication
B.To repair DNA damage caused by UV light
C.To remove damaged nucleotides
D.To fix double-strand breaks

4. What is the primary function of Nucleotide Excision Repair (NER)?

A.To remove bulky DNA lesions
B.To repair single-strand breaks
C.To fix mismatched base pairs
D.To repair DNA replication errors

5. Which enzyme is primarily responsible for removing damaged bases in BER?

A.DNA glycosylase
B.DNA polymerase
C.DNA ligase
D.AP endonuclease

6. Which repair pathway is typically used for DSBs in the G1 phase of the cell cycle?

A.Non-Homologous End Joining (NHEJ)
B.Homologous Recombination (HR)
C.Base Excision Repair (BER)
D.Nucleotide Excision Repair (NER)

7. Which enzyme is primarily responsible for detecting mismatched base pairs in MMR?

A.MutS
B.MutL
C.MutH
D.Exonuclease

8. Which of the following enzymes is critical for the incision step in NER?

A.XPG
B.DNA polymerase
C.Ligase
D.Helicase

9. True or False: BER can repair bulky DNA adducts.

A.True
B.False
C.Depends on the adduct
D.Only if they are small

10. What is the role of the Ku proteins in NHEJ?

A.They recognize double-strand breaks.
B.They participate in DNA replication.
C.They help in transcription regulation.
D.They initiate the cell cycle.

11. True or False: MMR repairs DNA lesions caused by oxidative damage.

A.True
B.False
C.It depends on the severity
D.Only in prokaryotes

12. True or False: NER is effective for repairing cytosine deamination.

A.True
B.False
C.Not applicable
D.Only in special cases

13. Fill in the blank: The first step in BER involves __________.

A.Recognition and removal of damaged base.
B.Gap filling with new nucleotides.
C.Sealing the DNA ends.
D.Creating a double-strand break.

14. Which of the following statements is true about NHEJ?

A.It is a fast but error-prone repair mechanism.
B.It requires a homologous template for repair.
C.It occurs primarily in the S phase of the cell cycle.
D.It always results in a precise repair of DNA.

15. Fill in the blank: MMR corrects __________ that occur during DNA replication.

A.mismatches
B.double-strand breaks
C.chromosomal rearrangements
D.bulk DNA lesions

16. What role does helicase play in the NER pathway?

A.Unwinds the DNA helix
B.Synthesizes new DNA strands
C.Recognizes DNA damage
D.Seals nicks in the DNA

17. What occurs immediately after DNA glycosylase acts in BER?

A.AP endonuclease cleaves the sugar-phosphate backbone.
B.DNA ligase seals the DNA.
C.DNA polymerase synthesizes the new base.
D.The damaged base is reinserted.

18. What is the function of the enzyme DNA-PKcs in DSB repair?

A.It phosphorylates proteins involved in NHEJ.
B.It removes damaged bases from DNA.
C.It promotes homologous recombination.
D.It seals nicks in DNA strands.

19. How do MMR and Nucleotide Excision Repair (NER) differ?

A.MMR fixes replication errors; NER repairs bulky DNA lesions
B.MMR repairs double-strand breaks; NER fixes mismatches
C.Both repair the same types of DNA damage
D.NER is only present in prokaryotes

20. Which of the following conditions is associated with defective NER?

A.Xeroderma pigmentosum
B.Base excision repair syndrome
C.Huntington's disease
D.Sickle cell anemia

21. How does BER differ from Nucleotide Excision Repair (NER)?

A.BER repairs single base damage; NER repairs bulky lesions.
B.BER is error-prone; NER is accurate.
C.NER operates only in prokaryotes; BER is for eukaryotes.
D.NER repairs mismatched bases; BER does not.

22. Which of the following is NOT a phase where Homologous Recombination (HR) is active?

A.G1 phase
B.S phase
C.G2 phase
D.M phase

23. What initiates the MMR process?

A.Presence of mismatched base pairs
B.UV radiation exposure
C.Chemical mutagens
D.DNA polymerase activity

24. Fill in the blank: The first step in NER involves _____.

A.Damage recognition
B.DNA synthesis
C.Ligation
D.Excision of damaged DNA

25. What type of DNA damage is commonly repaired by BER?

A.Deamination, oxidation, and alkylation of bases.
B.Double-strand breaks.
C.Bulky adducts from environmental toxins.
D.Replication errors.

26. During which step of HR do exonucleases play a critical role?

A.Trimming DNA ends to create overhangs.
B.Sealing broken DNA ends.
C.Recognizing double-strand breaks.
D.Ligating DNA ends together.

27. What function does MutH serve in the MMR process?

A.It cleaves the newly synthesized DNA strand
B.It detects mismatches in DNA
C.It repairs double-strand breaks
D.It synthesizes new DNA strands

28. What happens during the excision phase of NER?

A.The damaged DNA is synthesized anew
B.Endonucleases cut out the damaged section
C.Nicks are sealed in the DNA strand
D.Helicase unwinds the DNA

29. Which enzyme fills in the gap after base removal in Base Excision Repair?

A.DNA polymerase
B.DNA ligase
C.RNA polymerase
D.Topoisomerase

30. Which protein is essential for strand invasion during HR?

A.RAD51
B.Ku70/80
C.DNA-PKcs
D.Ligase IV

31. Which of the following types of mismatches is MMR NOT designed to correct?

A.Base substitutions
B.Double-strand breaks
C.Insertions
D.Deletions

32. Which of the following is NOT a step in the NER process?

A.Ligation
B.Damage recognition
C.Synthesis of RNA
D.Excision of damaged DNA

33. True or False: DNA ligase is crucial for completing the repair process in BER.

A.True
B.False
C.Only in eukaryotes
D.Only during NER

34. What is one consequence of unrepaired double-strand breaks?

A.Increased genomic stability.
B.Development of cancer.
C.Enhanced DNA replication fidelity.
D.Improved gene expression.

35. True or False: MMR is conserved across all life forms.

A.True
B.False
C.Only in bacteria
D.Only in multicellular organisms

36. How does NER differ from Base Excision Repair (BER)?

A.NER handles bulky lesions, while BER deals with base modifications
B.Both repair the same type of DNA damage
C.NER is slower than BER
D.Both involve the same enzymes

37. What is the primary role of AP endonuclease in BER?

A.It creates a nick in the DNA backbone at the apurinic/apyrimidinic site.
B.It synthesizes new DNA.
C.It identifies damaged bases.
D.It ligates DNA ends.

38. What distinguishes HR from NHEJ in terms of accuracy?

A.HR uses a homologous template.
B.HR is faster than NHEJ.
C.NHEJ requires a template.
D.NHEJ is always accurate.

39. What is a consequence of defective MMR?

A.Increased mutation rates
B.Enhanced DNA replication speed
C.Improved cellular repair mechanisms
D.Decreased cell division

40. What is the effect of a defective NER system on skin health?

A.Increased risk of skin cancer
B.Decreased collagen production
C.Improved skin elasticity
D.Reduced sensitivity to UV light

41. How does DNA glycosylase recognize damaged bases?

A.It scans DNA and recognizes altered base structures.
B.It uses RNA templates.
C.It relies on the presence of non-canonical bases.
D.It requires ATP for energy.

42. What happens at the Holliday junction during HR?

A.Genetic material is exchanged between homologous chromosomes.
B.DNA replication is initiated.
C.NHEJ is initiated.
D.Single-stranded DNA is formed.

43. Cause → Effect: A deficiency in MMR results in __________.

A.microsatellite instability
B.enhanced DNA repair
C.faster cell growth
D.decreased gene expression

44. Which protein is essential for the recognition of DNA damage in NER?

A.XPC
B.DNA ligase
C.DNA polymerase
D.XPG

45. Fill in the blank: In BER, after the gap is filled, __________ joins the ends.

A.DNA ligase
B.DNA helicase
C.DNA polymerase
D.Topoisomerase

46. Which of the following enzymes initiates the NHEJ process?

A.Ku proteins
B.RAD51
C.DNA ligase
D.Exonucleases

47. What role does exonuclease play in MMR?

A.It removes erroneous nucleotides
B.It synthesizes new DNA
C.It detects mismatches
D.It links detection to repair

48. What types of DNA damage are specifically targeted by NER?

A.Helix-distorting damage
B.Single base mismatches
C.Double-stranded breaks
D.Translocations

49. List the sequence of steps involved in BER.

A.Base removal - AP site formation - Nicking - Gap filling - Ligation
B.Nicking - Base removal - Ligation - Gap filling - AP site formation
C.Ligation - Base removal - AP site formation - Gap filling - Nicking
D.Gap filling - Ligation - Nicking - AP site formation - Base removal

50. In what scenario is HR primarily utilized?

A.During DNA replication when sister chromatids are available.
B.In response to oxidative stress.
C.For repairing single-strand breaks.
D.During RNA transcription.

51. Identify the primary difference between MMR and Base Excision Repair.

A.MMR fixes mismatched bases; Base Excision Repair fixes damaged bases
B.Both mechanisms operate on the same types of errors
C.Base Excision Repair is only for prokaryotes
D.MMR is more error-prone than Base Excision Repair

52. What role does DNA polymerase play in the NER process?

A.Seals nicks in the DNA
B.Synthesizes new DNA to fill gaps
C.Unwinds the DNA
D.Recognizes damaged DNA

53. True or False: BER is generally error-prone and leads to mutations.

A.True
B.False
C.Only under certain conditions
D.Depends on the type of damage

54. What is the primary function of Ligase IV in NHEJ?

A.To ligate broken DNA ends.
B.To trim DNA ends.
C.To facilitate strand invasion.
D.To phosphorylate repair proteins.

55. Provide a short example of MMR in action.

A.During replication, if cytosine pairs with adenine, MutS detects it
B.When DNA is exposed to radiation, repair occurs
C.When a strand break happens, it's fixed
D.Before replication starts, errors are corrected

56. During which phase of NER is ligase used?

A.Damage recognition
B.Excision
C.DNA synthesis
D.Ligation

57. What role does DNA polymerase play in the context of BER?

A.It synthesizes the correct base to replace the removed one.
B.It recognizes damaged bases.
C.It ligates the DNA ends.
D.It creates single-strand breaks.

58. Which process is faster: NHEJ or HR?

A.NHEJ
B.HR
C.Both are equally fast.
D.Neither process is fast.

59. True or False: MMR is only found in eukaryotic cells.

A.True
B.False
C.Only in yeast
D.Only in mammals

60. True or False: NER operates only in the nucleus of eukaryotic cells.

A.True
B.False
C.Only during cell division
D.In both the nucleus and cytoplasm

61. Which of the following statements about Base Excision Repair (BER) is NOT true?

A.BER repairs only single-base lesions in DNA.
B.DNA ligase seals the final nick in the DNA strand during BER.
C.AP endonuclease is involved in the initial recognition of damaged bases.
D.DNA glycosylase initiates the BER process by removing damaged bases.

62. Which of the following statements best describes the Non-Homologous End Joining (NHEJ) repair process?

A.It directly ligates broken DNA ends without a template, making it faster and more error-prone.
B.It requires a homologous template for accurate repair, making it slower and more precise.
C.It only functions during the S phase of the cell cycle when sister chromatids are present.
D.It is initiated by the recognition of single-strand breaks in DNA.

63. Name a disease condition associated with defects in MMR.

A.Lynch syndrome
B.Sickle cell anemia
C.Cystic fibrosis
D.Down syndrome

64. Which of the following best describes the primary damage that Nucleotide Excision Repair (NER) addresses?

A.Bulky, helix-distorting lesions
B.Single-strand breaks
C.Oxidative base damage
D.Mismatched bases

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