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(DEC 2003)
25. Type of proofreading activity bv DNA
polymerase I in E.coli is
(1) 5’-3’ exonuclease
(2) 5'-3' endonuclease
(3) 3'-5' exonuclease
(4) 3'-5' endonuclease
(DEC 2010)
26. Among the following which iS termed as
proof reading activity of DNA polymerase?
(1) 5'→3' polymerase activity
(2) 3’→5’ polymerase activity
(3) 5'→3' exonuclease activity
(4) 3'→5’ exonuclease activity
(JUNE 2012)
24. Double stranded DNA replicates in a (DEC 2008)
semi-conservative manner. In an in vitro DNA 27. Among the following which activity is
synthesis reaction, dideoxy CTP and, dideoxy absent in bacterial DNA polymerase I
CMP were individually added in excess (in (1) 5’→3’ Polymerase activity
separate reaction tubes) in addition to dNTPs (2) 3’→5’ Polymerase activity
and other necessary reagents. Rate of DNA (3) 5'→3’ Exonuclease activity
Synthesis was measured by incorporation of (4) 3'→5' Exonuclease activity
3H-thymidine. The four graphs drawn below
represent the rate of DNA synthesis in two (DEC 2015)
separate reaction tubes. 28. In eukaryotic replication, helicase loading
Which of the following graphs represents the occurs at all replicators during
expected data? (1) Go phase (2) G1 phase
(3) S phase (4) G2 phase
(DEC 2011) (JUNE 2018)
29. While replicating DNA, the rate of mis- 32. E. coli takes 40 min. to duplicate its
incorporation by DNA polymerase is 1 in 105 genome using a bi-directional mode of
nucleotides. However, the actual error rate in replication. If E. coli were to use
the replicated DNA is 1 in 109 nucleotides uni-directional mode of replication to
incorporated. This is achieved mainly due synthesize a full copy of DNA complementary
to to just one of the strands of the genome, it
(1) spontaneous excision of mis-incorporated would take
Nucleotides (1) 40 min (2) 80 min
(2) 3'→5' proofreading activity of DNA (3) 20 min (4) 60 min
polymerase
(3) termination of DNA polymerase at mis- (JUNE 2016)
incorporated sites 33. In E. coli grown under nutrient rich
(4) 5'→3’ proof reading activity conditions, replication of entire genome takes
about 40 min., yet it can divide every 20 min.
(DEC 2017) This is so because:
30. In all organisms, it is critical that (1) While E. coli divides every 20 min, equal
replication initiation be tightly controlled to transfer of genetic material occurs only in the
ensure that chromosome number and cell alternate rounds of cell divisions.
number remain appropriately balanced. Given (2) A second round of genome replication
below are several statements regarding begins before the completion of first round of
regulation of replication in E. coli. replication, and by the time cell is ready to
A. Hemi-methylation and sequestration of divide, two copies of the genome are
oriC (origin of replication) by a protein called available.
SeqA prevents initiation of replication. (3) Genome replication cell division are not
B. Availability of DnaA protein is an important coordinated with each other.
requirement for initiation of replication. (4) During cell division, only one of the
C. The ratio of ADP : ATP is important as high strands of the genome whose synthesis can
level of ADP is required for initiation of be achieved in 20 min, is transferred to the
replication. daughter cell.
D. Recruitment of Hda protein by sliding
clamp inhibits ATP hydrolysis required for (DEC 2002)
initiation of replication. 34. Speed of DNA replication in mammals is
Which of the above statements are NOT true? 256 bp/sec, so for replication of 3X109 bp
(1) A and B (2) B and C DNA it will take a very long time, but it is
(3) C and D (4) D and A completed within few hours because
(1) Most of DNA is intron
(DEC 2015) (2) High amount of Repetitive DNA
31. It takes 40 minutes for a typical E. coli (3) Multiple origin of replication
cell to completely replicate its chromosome. (4) Only small portion is replicated in one
Simultaneous to the ongoing replication, 20 cycle
minutes of a fresh round of replication is
completed before the cell divides. What (JUNE 2006)
would be the generation time of E. coli 35. If bacterial genome and plasmid are
growing at 37oC in complex medium? allowed to replicate in same manner using
(I) 20 minutes same replication machinery then
(3) 60 minutes (1) Plasmid DNA will complete replication first
(2) 40 minutes (2) Bacterial DNA will complete replication
(4) 30 minutes first
(3) Both will replicate at same time
(4) It depends on GC content of both DNA
(JUNE 2016) B. Among the Okazaki fragments, synthesis
36. Two experiments were performed. In the of (iv) occurs prior to the synthesis of (iii) and
first one, Okazaki fragments were prepared (i)
from a replicating cell of E. coli grown in the C. Among the Okazaki fragments, synthesis
presence of 32P. In the other, the two strands of (ii) occurs prior to the synthesis of (iii) and
of E. coli chromosome were separated (iv).
into a H strand and L strand, immobilized Which one of the following options represents
onto a nitrocellulose membrane and the correct statement(s)?
hybridized with the Okazaki fragments (1) A only (2) B only
prepared in the first experiment. (3) A and B (4) A and C
Which one of the following options correctly
describes the observation? (FEB 2022-II)
(1) Okazaki fragments will hybridize to only H
strand
(2) Okazaki fragments will hybridize to only L
strand
(3) Okazaki fragments will hybridize with both
H and L strands
(4) Because the H and L strands have been
prepared from different cultures of E. coli, the
Okazaki fragments will hybridize to neither
(JUNE 2002)
37. Telomeres consist of 39. In the figure above, replication of DNA
(1) Simple tandem repeats beginning from the origin of replication of the
(2) Nucleolar organizer region chromosome of a newly identified bacterium
(3) GC rich sequences having a double stranded circular DNA
(4) Single copy repeats genome is shown. Characterization of DNA
polymerase responsible for genome
(DEC 2019) replication showed that DNA synthesis
38. The figure below shows the structure of a occurred in to direction and it depends on the
replication fork. presence of a primer (as is the case in
Escherichia coli). Polarities ot DNA (5' or 3')
are as shown. Replication begjns at a point
marked ‘O’ on the left of the bubble. and
both the parent strands were replicated
concurrently. The longer arrow inside the
bubble shows the leading strand, whereas
the shorter arrows (marked a, b, c) show the
Okazaki fragments. The model depicts a:
(i) bidirectional mode of replication wherein
synthesis of the Okazaki fragment marked 'c'
occurs prior to those marked 'a' and 'b'
(2) bidirectional mode of replication wherein
synthesis of the Okazaki fragment marked 'a'
occurs prior to those marked 'b' and 'c'
(3) unidirectional mode of replication wherein
Based on this information following synthesis of the Okazaki fragment marked 'c'
statements are made: occurs prior to those marked 'a' and 'b'.
A. (i) represents the leading strand while (ii), (4) unidirectional mode of replication wherein
(ii) and (iv) represent the Okazaki fragments. synthesis of the Okazaki fragment marked 'a'
occurs prior to those marked 'b' and 'c'.
(SEPT 2022- II) (MODEL PAPER)
40. The long DNA strand depicted below is 43. DNA repair, synthesis and recombination
serving as a template for lagging strand DNA are intimately connected and inter
synthesis. dependent. An apparent commonality
between processes of DNA replication
and repair in the enzymatically catalyzed
synthesis of DNA polynucleotide segments,
which can be assembled with pre-existing
polynucleotides, leading to repair or
replication. Synthesis of these polynucleotide
The short lines represent the newly segments is catalyzed by a group of enzymes
synthesized okazaki fragments. DNA-dependant DNA polymerases. In the
At which position among A, B, C and D would case of E.coli, DNA polymerase has been
DNA primase act next? isolated in three distinct forms whereas five
(1) A (2) B main types of polymerase have been isolated
(3) C (4) D from mammalian cells. All the polymerases
synthesize polynucleotides only in the 5'→3'
(DEC 2019) direction. If polynucleotide chains could be
41. In the diagram below, the dotted line elongated in 3’→5' direction, the hypothetical
marks the point of initiation of bidirectional growing 5' terminus, rather than the
replication incoming nucleotide, would carry a tri-
c, phosphate that is unsuitable for further
elongation. The 3'→5' exonuclease activity is
not associated with all the polymerases and
only present in
(A) All E. coli DNA polymerases
(B) Pol l, Pol IV, Pol V, Pol α, Pol β.
(C) Pol l, Pol III, Poi Ꟙ, Poi ϵ
A. On the right side of the dotted line, leading (D) Pol l, Pol IV, POl α, Poi ϵ.
strand synthesis occurs using the upper The correct statements are
strand as the template. (1) (A) and (B) (2) (A), (B) and (C)
B. On the right side of the dotted line, leading (3) (C) only (4) (A), (C) and (D)
strand synthesis occurs using the lower
strand as the template. (JUNE 2010)
C. A ligase deficient (lig-) mutant would affect 44. Among the following which DNA
replication of the upper strand on the left polymerase lacks proof reading activity?
side of the dotted line. (1) DNA polymerase α primase activity
D. A ligase deficient (lig-) mutant would affect (2) DNA polymerase Ꟙ
replication of the lower strand on the left side (3) DNA polymerase ϵ
of the dotted line. (4) Both DNA polymerase α and ϵ
Which one of the following options represents
the combinations of the correct statements? (JUNE 2008)
(1) A and D (2) B and C 45. Which of the following statement is
(3) B and D (4) A and C correct with reference to replication in
eukaryotes?
(DEC 2014) (1) Single origin and continuous replication
42, During replication, the RNA primer is (2) Multiple origin and semi-discontinuous
degraded by the 5' - 3' exonuclease activity replication
of (3) Multiple origin and continuous replication
(1) RNAse H (4) Single origin and semi-discontinuous
(2) FEN-1 (flap endonuclease 1) replication Nick translation means
(3) Topoisomerase II B
(4) DNA polymerase
(JUNE 2010) (JUNE 2023-II)
46. Nick translation means 49. A mutant DNA polymerase was found to
(1) Translation by cytosolic ribosome have higher error rate and synthesized only
(2) Translation of protein from stalled sites short DNA fragments. In the statements
(3) Replication by ONA polymerase I after below, potential explanations are given.
removing RNA primers A. The 5' to 3' exonuclease activity is
(4) Replication of DNA by DNA polymerase I compromised.
from nicks produced by DNase treatment B. The 3' to 5' exonuclease activity is
compromised.
(JUNE 2019) C. The polymerase tends to frequently
47. for Escherichia coli chromosomal DNA dissociate from the template.
replication, which one of the following D. The polymerase is unable to unwind the
statements is true? DNA template during replication.
(1) DNA polymerase I is the main polymerase Which one of the following options represents
required for DNA replication the combination of all correct statements?
(2) DNA polymerase I though identified (1) A and B (2) C and D
originally by Kornberg as the one responsible (3) A and D (4) B and C
for replication, is not important for the DNA
replication process (JUNE 2023-I)
(3) Requirement of DNA polymerase I is in 50. The following statements refer to factors
the context of removal of RNA primer needed regulating the fidelity of DNA replication.
for DNA synthesis, and then fill in the same A. The 5' to 3' exonuclease activity of the
with DNA equivalent replicative DNA polymerase.
(4) DNA polymerase I is the primary enzyme B. Imbalanced intracellular concentrations of
for error prone DNA synthesis in response to the four dNTPs.
SOS. C. Increased intracellular concentrations of
INTPs resulting in increased incorporation of
(SEPT 2022-II) rNTPs during DNA synthesis, which are not
48. The following statements refer to the E. easily removed by the polymerase's proof-
coli replicative DNA polymerase: reading activity.
(A) DNA POI I displays very limited D. Removal of incorrectly incorporated
processivity and possesses 3’→5' exonuclease nucleotides by the mismatch repair system.
activity, allowing fidelity of DNA replication. Which one of the following options gives the
(B) DNA POI III is suitable for leading strand combination of all correct statements?
DNA synthesis due to its high processivity (1) A and D only (2) B, C and D
and 5→3' exonuclease activity that removes (3) B and C only (4) A, B and D
incorrect nucleotides incorporated during
DNA synthesis. (JUNE 2019)
(C) DNA POI I possesses 5→3' exonuclease 51. During replication, RNaseH removes all of
activity which allows removal of the RNA the RNA primer except the ribonucleotide
primer while its 3' polymerase activity allows directly linked to the DNA end. This is
it to fill the gap created by removal of the because
RNA primer (1) it can degrade RNA and DNA end. From
(D) DNA POI III is suitable for lagging strand their 5' end.
DNA synthesis due to its low processivity and (2) it can only cleave bonds between two
5’→3' exonuclease activity. ribonucleotides.
Which one of the options below represents (3) it can degrade RNA and DNA from their 3'
the combination of all correct statements? end.
(1) D only (2) B and C (4) activity of RNaseH is inhibited by the
(3) A and B (4) A and C presence of duplex containing both strands
as DNA.
(DEC 2010) (ii) Adenylyl group of NAD+ is transferred to
52. In prokaryotes during replication, the the ϵ-amino group of Lys in DNA ligase to
lagging strand is synthesized in a series of form a phosphoamide adduct.
short fragments known as Okazaki fragments, (iii) DNA ligase catalyses the formation of a
consequently requiring many primers. The phosphodiester bond by the nucleophilic
RNA primers of Okazaki fragments are attack of the 3' hydroxyl group onto the
subsequently degraded by DNA polymerase I phosphate and releases AMP.
and the gap are filled. How DNA polymerase I Based on the statements made above,
fills the gap once the primer have been identify the correct sequence of the reaction
removed from lag ging stand? steps.
(1) DNA polymerase I has its own primer (1) (i)-(ii)-(iii) (2) (i)-(iii)-(ii)
(2) DNA polymerase I do not require primer (3) (ii)-(i)-(iii) (4) (iii)-(i)-(ii)
(3) DNA from leading stand serves as primer
(4) 3'-ends of existing Okazaki fragments on (FEB 2022-I)
lagging stand serves as primer 57. Which one of the following proteins is
essential for both the initiation of DNA
(JUNE 2019) replication as well as the continued
53. In a human cell line, a large fraction of advance of the replication fork?
double-strand DNA breaks are repaired by (1) ORC (2) Geminin
non-homologous end joining (NHEJ). An (3) Cdc45 (4) Cdc6
inhibitor of FLAP endonuclease will affect
(1) recruitment of DNA—dependent kinase (NOV 2020-II)
(2) gap trimming 58. The followjng statements are made with
(3) DNA unwinding reference to the replication of DNA.
(4) pairing of micro-homology regions. A. The eukaryotic counterpart of the bacterial
B- clamp protein is proliferating cell nuclear
(JUNE 2017) antigen (PCNA)
54 In eukaryotic replication, priming of DNA B. Mutation inactivating one of the subunits
synthesis and removal of RNA catalyzed by of the Mcm 2-7 complex negatively affects
(1) DNA Pol α and PCNA, respectively the initiation of DNA replication in eukaryotes,
(2) DNA Pol α and FEN 1, respectively but has no effect on elongation of the
(3) DNA Pol Ꟙ and FEN 1, respectively. replication fork
(4) DNA Pol ϵ and PCNA, respectivelv. C. All DNA polymerases responsible for
replicating the eukaryotic genome catalyze
(JUNE 2008) DNA chain extenston jn a DNA template-
55. In eukaryotes shortening of dependent manner.
chromosomes from ends is prevented bv D. The FENI protein plays a role in the
(1) DNA polymerase (2) RNA polymerase synthesis of the lagging strand during DNA
(3) Telomerase (4) Transposase replication as well as in base excision repair
1-2 21 - 3 41 - 3 61 - 4 81 - 4
2-4 22 - 1 42 - 2 62 - 1 82 - 2
3-1 23 - 3 43 - 3 63 - 1 83 - 3
4-3 24 - 1 44 - 1 64 - 1 84 - 2
5-4 25 - 3 45 - 2 65 - 1 85 - 2
6-3 26 - 4 46 - 4 66 - 4 86 - 2
7-4 27 - 2 47 - 3 67 - 4 87 - 4
8-2 28 - 2 48 - 4 68 - 4 88 - 4
9-4 29 - 2 49 - 4 69 - 1
10 - 1 30 - 3 50 - 2 70 - 1
11 - 3 31 - 1 51 - 2 71 - 3
12 - 2 32 - 2 52 - 4 72 - 2
13 - 1 33 - 2 53 - 2 73 - 4
14 - 3 34 - 3 54 - 2 74 - 4
15 - 1 35 - 1 55 - 3 75 - 3
16 - 2 36 - 3 56 - 3 76 - 1
17 - 4 37 - 1 57 - 3 77 - 3
18 - 4 38 - 3 58 - 2 78 - 4
19 - 2 39 - 3 59 - 3 79 - 3
20 - 3 40 - 4 60 - 3 80 - 2