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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centromere
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telomere
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centrosphere
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chromomere
A
Correct answer
Explanation
It is the structure in the chromosome which gives it shapes like I, V, L, etc.
C
Correct answer
Explanation
Total number of chromosomes in the gamete of fruit fly is 4.
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Butterfly
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Housefly
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Ophioglossum
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Apple
C
Correct answer
Explanation
Ophioglossum has 1260 chromosomes.
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Y chromosome
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X chromosome
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a pair of X and Y chromosomes
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no chromosomes
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a pair of X and X chromosomes
B
Correct answer
Explanation
An unfertilised egg always has an X chromosome.
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Deletions
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Duplications
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Robertsonian translocation
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Isochromosome
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Inversions
C
Correct answer
Explanation
A Robertsonian translocation in balanced form results in no excess or deficit of genetic material and causes no health difficulties. In unbalanced forms, Robertsonian translocations cause chromosomal deletions or addition and result in syndromes of multiple malformations, including trisomy 13 (Patau syndrome) and trisomy 21 (Down syndrome).
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Trisomy 21
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Chromosome 7
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Tetrasomy 9p
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Tetrasomy 18p
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Chromosome 17
B
Correct answer
Explanation
In squamous cell carcinoma, a protein from the epidermal growth factor receptor (EGFR) gene is often overexpressed in conjunction with polysomy of chromosome 7, so chromosome 7 can be used to predict the presence of EGFR in squamous cell carcinoma.
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47, XXY
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47, XYY
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XX male syndrome
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mixed gonadal dysgenesis
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45, X Turner syndrome
E
Correct answer
Explanation
Turner syndrome 45, X encompasses several conditions in human females, of which monosomy X (absence of an entire sex chromosome, the Barr body) is most common. It is a chromosomal abnormality in which all or part of one of the sex chromosomes is absent or has other abnormalities.
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Translocation
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Deletion
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Duplication
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Frame shift
A
Correct answer
Explanation
The exchange of chromosomes segments between non-homologous chromosomes is called translocation.
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Chromosome 1
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Chromosome 2
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X-Chromosome
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Y-Chromosome
D
Correct answer
Explanation
The chromosome which carry the least number of genes (i.e. only 231) is Y-Chromosome.
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Monosomy
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Disomy
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Trisomy
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Tetrasomy
A
Correct answer
Explanation
Monosomy refers to lack of one chromosome of the normal complement. Partial monosomy can occur in unbalanced translocations or deletions, in which only a portion of the chromosome is present in a single copy. Monosomy of the sex chromosomes (45X) causes Turner syndrome.
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Loss of heterozygosity
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Inversion
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Interstitial deletions
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Chromosome translocation
D
Correct answer
Explanation
In genetics, a chromosome translocation is a chromosome abnormality caused by rearrangement of parts between nonhomologous chromosomes. A gene fusion may be created when the translocation joins two otherwise separated genes, the occurrence of which is common in cancer.
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Can be grown easily in the laboratory
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Long generation time
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Easily distinguishable males and females
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Only four pairs of chromosomes
B
Correct answer
Explanation
It has a short generation time (about 10 days at room temperature) so several generations can be studied within a few weeks.
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locus
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chromosome
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allele
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gene
D
Correct answer
Explanation
A gene is a unit of heredity in a living organism. It is a name given to some stretches of DNA and RNA that code for a type of protein or for an RNA chain that has a function in the organism. Living things depend on genes, as they specify all proteins and functional RNA chains.
C
Correct answer
Explanation
The Y chromosome is the sex-determining chromosome in humans. Females have XX chromosomes while males have XY chromosomes. Presence of the Y chromosome determines male sexual characteristics during development.
A
Correct answer
Explanation
Males have one X chromosome and one Y chromosome (XY sex determination). The X chromosome comes from the mother and the Y chromosome from the father. Females have two X chromosomes (XX).