Selected MCQ

Current Question
Which term describes genes that are located on the same chromosome and inherited together more often than by chance?
  • A. Linked genes
  • B. Epistatic genes
  • C. Polygenic genes
  • D. Independent genes
Correct Answer: A
Explanation:
Linked genes are near each other on the same chromosome. They tend to be inherited together, and their recombination frequency is less than 50%.
Related Question 1
Phenylketonuria (PKU) is inherited as an autosomal recessive trait. If two carriers have a child, what is the probability the child will be unaffected (no mutant alleles)?
  • A. 100%
  • B. 75%
  • C. 50%
  • D. 25%
Correct Answer: B
Explanation:
For two carriers (Aa × Aa), the offspring genotype ratio is 1 AA: 2 Aa: 1 aa. 75% (AA + Aa) are unaffected (though 50% are carriers).
Related Question 2
What is the fundamental unit of heredity that occupies a specific locus on a chromosome?
  • A. Base pair
  • B. Gene
  • C. Chromatin
  • D. Nucleotide
Correct Answer: B
Explanation:
A gene is the hereditary unit at a chromosome locus. It consists of DNA sequences encoding a functional product (RNA or protein).
Related Question 3
Which of the following best describes polygenic inheritance?
  • A. One gene affects multiple traits (e.g., pleiotropy)
  • B. Many genes contribute to one trait (e.g., skin color)
  • C. A trait determined by genes only on the X chromosome
  • D. Inheritance of mitochondrial DNA
Correct Answer: B
Explanation:
Polygenic inheritance means multiple genes (often with additive effects) determine a single phenotype, such as height or skin color, producing continuous variation.
Related Question 4
Down syndrome (trisomy 21) results in how many total chromosomes in a karyotype?
  • A. 45
  • B. 46
  • C. 47
  • D. 48
Correct Answer: C
Explanation:
Down syndrome is caused by an extra copy of chromosome 21. Humans normally have 46 chromosomes; trisomy adds one extra, making 47.
Related Question 5
In genomic imprinting, the expression of a gene depends on its parental origin. For example, only the paternally inherited allele of a certain gene is expressed. This is known as:
  • A. Epigenetic modification
  • B. Loss of heterozygosity
  • C. Imprinting
  • D. Mendelian inheritance
Correct Answer: C
Explanation:
Genomic imprinting is an epigenetic phenomenon where only one allele (maternal or paternal) is expressed, depending on the parent of origin, while the other is silenced.