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DNA Replication Questions
Q.
DNA replication is described as semiconservative because:
Each daughter molecule has one parental and one newly synthesized strand
Both parental strands stay together in one daughter
Both daughter strands are entirely new
Only one daughter molecule is produced
Explanation:
Each daughter DNA molecule contains one parental (conserved) strand and one newly synthesized strand.
Q.
The Meselson-Stahl experiment used which isotope to demonstrate semiconservative replication?
Phosphorus-32 (32P)
Nitrogen-15 (15N)
Carbon-14 (14C)
Sulfur-35 (35S)
Explanation:
Meselson and Stahl (1958) labeled DNA with heavy nitrogen (15N) and tracked its distribution in successive generations using density gradient centrifugation.
Q.
Sites on DNA where replication initiates are called:
Origins of replication
Telomeres
Promoters
Centromeres
Explanation:
Origins of replication are specific DNA sequences recognized by initiator proteins that recruit the replication machinery.
Q.
The Y-shaped structure where DNA is being unwound and copied is called the:
Replication fork
Okazaki fork
Replisome
Promoter region
Explanation:
The replication fork is the site where parental DNA is separated into two template strands and new DNA is synthesized.
Q.
Which enzyme unwinds the DNA double helix at the replication fork?
DNA polymerase
Primase
Ligase
DNA helicase
Explanation:
DNA helicase uses ATP hydrolysis to break hydrogen bonds between base pairs and separate the two strands.
Q.
Which enzyme synthesizes RNA primers during DNA replication?
Primase
Topoisomerase
DNA polymerase III
DNA ligase
Explanation:
Primase is an RNA polymerase that creates short RNA primers, providing a 3'-OH for DNA polymerase to extend.
Q.
DNA polymerase can only add nucleotides to which end of a growing strand?
The 5' end
Both ends simultaneously
Only the middle of the strand
The 3' end
Explanation:
DNA polymerases synthesize DNA strictly in the 5'→3' direction, adding to the free 3'-OH end of the growing chain.
Q.
The strand synthesized continuously toward the replication fork is called the:
Leading strand
Coding strand
Lagging strand
Template strand
Explanation:
The leading strand is synthesized in the same direction as fork movement (5'→3'), so it grows continuously with a single primer.
Q.
The strand synthesized discontinuously in short fragments is called the:
Leading strand
Non-template strand
Sense strand
Lagging strand
Explanation:
The lagging strand is synthesized away from the fork direction in short Okazaki fragments, each requiring its own primer.
Q.
The short DNA fragments synthesized on the lagging strand are called:
Watson fragments
Klenow fragments
Okazaki fragments
Kornberg fragments
Explanation:
Okazaki fragments are typically 100–200 nt in eukaryotes and 1000–2000 nt in prokaryotes; they are later joined by DNA ligase.
Q.
The enzyme that joins Okazaki fragments together is:
Topoisomerase
DNA helicase
DNA polymerase I
DNA ligase
Explanation:
DNA ligase seals the nick between adjacent fragments by forming a phosphodiester bond between the 3'-OH and 5'-phosphate.
Q.
In E. coli, which DNA polymerase is primarily responsible for chromosomal DNA replication?
DNA polymerase IV
DNA polymerase II
DNA polymerase III
DNA polymerase I
Explanation:
DNA polymerase III is the main replicative enzyme in E. coli, with high processivity and 3'→5' proofreading exonuclease activity.
Q.
In E. coli, which DNA polymerase removes RNA primers and fills the resulting gaps?
DNA polymerase III
Primase
DNA polymerase II
DNA polymerase I
Explanation:
DNA polymerase I possesses a unique 5'→3' exonuclease activity that removes RNA primers while simultaneously extending the DNA chain.
Q.
Which exonuclease activity enables DNA polymerase to remove mismatched nucleotides during replication?
5'→3' exonuclease activity
Endonuclease activity
3'→5' exonuclease activity
Helicase activity
Explanation:
The 3'→5' exonuclease activity provides proofreading, removing incorrectly incorporated nucleotides and increasing replication fidelity.
Q.
Single-strand binding proteins (SSBs) function during replication to:
Add supercoils to DNA
Cleave phosphodiester bonds
Prevent re-annealing of separated DNA strands
Synthesize RNA primers
Explanation:
SSBs coat single-stranded DNA to prevent premature re-annealing and to protect the strands from nucleases.
Q.
In bacteria, which enzyme introduces negative supercoils ahead of the replication fork?
DNA gyrase
DNA polymerase I
DNA helicase
DNA ligase
Explanation:
DNA gyrase (a type II topoisomerase) uses ATP to introduce negative supercoils, relieving positive torsional stress generated by fork progression.
Q.
Telomerase functions to:
Synthesize mitochondrial DNA
Cleave Okazaki fragments
Extend chromosome ends using an RNA template
Remove RNA primers
Explanation:
Telomerase is a reverse transcriptase that uses its own RNA template to extend telomeric repeats at chromosome ends, compensating for end-replication loss.
Q.
Eukaryotic chromosomes typically have how many origins of replication per chromosome?
Exactly one origin
No fixed origins
Multiple origins
Two origins only
Explanation:
Eukaryotic chromosomes are long and replicate from multiple origins, allowing genome duplication within a single S phase.
Q.
Replication that proceeds in both directions away from a single origin is described as:
Unidirectional replication
Rolling circle replication
Bidirectional replication
Conservative replication
Explanation:
Bidirectional replication creates two replication forks moving in opposite directions from each origin, doubling the rate of genome duplication.
Q.
The high fidelity of DNA replication (error rate ~1 in 10^9) is achieved by:
Random chance alone
Only base selection by DNA polymerase
Base selection, proofreading, and mismatch repair
Only post-replication repair
Explanation:
Base selection, 3'→5' proofreading exonuclease activity, and post-replication mismatch repair together produce the extremely low error rate observed.
Q.
Which of the following is NOT required for DNA replication?
RNA polymerase
Primase
dNTPs
DNA template
Explanation:
RNA polymerase is the enzyme for transcription. DNA replication requires a template, primers, dNTPs, and the replisome proteins, not RNA polymerase.
Q.
Okazaki fragments are found on which strand?
Neither strand
Leading strand
Lagging strand
Both strands equally
Explanation:
Okazaki fragments are exclusively synthesized on the lagging strand because this strand must be synthesized in short segments away from fork movement.
Q.
Primers in DNA replication are made of:
RNA
Protein
DNA
Polysaccharide
Explanation:
Primase synthesizes short RNA primers (not DNA) because DNA polymerases can only extend an existing 3'-OH group, which RNA primers provide.
Q.
The replisome is best described as:
A DNA repair enzyme
The multiprotein complex that carries out DNA replication
A type of topoisomerase
A ribosome-bound complex
Explanation:
The replisome is the multiprotein machine at the replication fork composed of helicase, primase, DNA polymerases, and accessory factors.
Q.
Which of the following organisms uses a theta (θ) structure during DNA replication?
Mitochondria only
Bacteria with circular chromosomes
Eukaryotic linear chromosomes
Retroviruses only
Explanation:
Theta replication occurs in circular DNA molecules such as bacterial chromosomes and plasmids, producing a characteristic θ-shaped intermediate.