Biology
Cell Cycle and Chromosomes
1,348 Questions
Explore a curated list of questions covering the cell cycle, mitosis, and meiosis. Topics include DNA replication, chromosomal structures, and genetic disorders. This material is essential for students preparing for biology and general science competitive exams.
Cell cycle eventsDNA replicationMeiosis processChromosomal structuresGenetic disorders
Cell Cycle and Chromosomes Questions
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inversion
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translocation
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deletion
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duplication
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recombination
A
Correct answer
Explanation
As the genes get rotated within a chromosome by 180 degrees, the position of genes gets changed.
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Translocation
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Inversion
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Frame shift
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Hyperploidy
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Hypoploidy
C
Correct answer
Explanation
Addition or deletion alters the reading frame of all base triplets in the gene distal to the mutation.
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Autosomal mutation
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Germ mutation
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Lethal mutation
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Chromosomal mutation
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Point mutation
B
Correct answer
Explanation
Affects germ cells and is inherited from one generation to the next generation
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Turner's syndrome
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Down's syndrome
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Klinefelter's syndrome
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Edward's syndrome
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Cri-du-chat syndrome
B
Correct answer
Explanation
It has three 21 number chromosomes.
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Deletion
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Duplication
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Inversion
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Translocation
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All of the above
E
Correct answer
Explanation
All deletion, duplication, inversion and translocation lead to structural change in chromosomes.
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Deletion
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Duplication
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Inversion
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Translocation
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Recombination
B
Correct answer
Explanation
Due to addition or replication of one or more genes, the chromosomes become longer.
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chromosomal aberration
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point mutation
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spontaneous mutation
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induced mutation
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transformation
B
Correct answer
Explanation
It is the change in the number or arrangement of nucleotides.
It is the transfer of DNA from one bacterium to the other.
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Lung cancer
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Chronic lymphoblastic leukemia
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Acute myelocytic leukemia
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Chronic myelogenous leukemia
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Bladder cancer
D
Correct answer
Explanation
Chronic myelogenous leukemia (CML) is caused by the Philadelphia chromosome, resulting from a reciprocal translocation between chromosomes 9 and 22 - t(9;22)(q34;q11). This creates the BCR-ABL fusion gene with constitutive tyrosine kinase activity. Other malignancies listed have different causes (lung cancer from mutations, CLL from various genetic changes, AML from multiple mutations, bladder cancer from environmental factors).
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Western blot
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Northern blot
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Southern blot
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FISH
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ELISA
D
Correct answer
Explanation
FISH (Fluorescence In Situ Hybridization) is the standard screening test for aneuploidy syndromes like Down syndrome, Turner syndrome, etc. It uses fluorescent probes to detect chromosomal abnormalities.
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C-banding
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R-banding
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G-banding
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Q-banding
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T-banding
D
Correct answer
Explanation
Q-banding is a fluorescent pattern obtained using quinacrine for staining. The pattern of bands is very similar to that seen in G-banding. They can be recognised by a yellow fluorescence of differing intensity. Most part of the stained DNA is heterochromatin. Quinacrin (atebrin) binds both regions rich in AT and in GC, but only the AT-quinacrin-complex fluoresces.
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Centromere protein
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Centromere protein B
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Centromere protein C 1
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Centromere-associated protein E
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Centromere protein F
C
Correct answer
Explanation
Centromere protein C 1 is a centromere autoantigen and a component of the inner kinetochore plate. The protein is required for maintaining proper kinetochore size and a timely transition to anaphase. A putative pseudogene exists on chromosome 12.
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Metaphase
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Telophase
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Anaphase
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Prophase
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Interphase
E
Correct answer
Explanation
Interphase occurs just prior to cell division. Prepubertal male primordial germ cells are reactivated from interphase at puberty and enter rounds of mitoses followed by meiosis 1 and 2 to produce unique haploid sperm.
B
Correct answer
Explanation
A human body has 23 pairs of chromosomes, out of which 22 pairs are autosomes and 1 pair is the sex determining pair.
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1 pair
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22 pairs
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8 pairs
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16 pairs
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2 pairs
B
Correct answer
Explanation
Chromosomes that do not take part in the determination of sex are called autosomes. There are 22 pairs of autosomes in a human. This is the correct option. A human being has 22 pairs of autosomes and only 1 pair of allosomes.
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XX, XY
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XY, XX
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XX, XO
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XO, XX
B
Correct answer
Explanation
Human females have two of the same kind of sex chromosomes (XX), while males have two distinct sex chromosomes (XY). The XY chromosomal cells create testosterone and anti-müllerian hormone to turn the genderless sex organs into male. With females, their cells excrete estrogen, driving the body down the female pathway. Thereby, determining the sex of the baby.