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MDCAT · Biology

Inheritance and Genetics MCQs for MDCAT

50 practice MCQs on Mendel's laws, alleles, dominance, sex-linkage, chromosomes, mutations and pedigree analysis. Every question has the correct answer and an explanation.

Start free — 20 questions

Inheritance and Genetics is part of the MDCAT Biology syllabus. This page collects Inheritance and Genetics MCQs in the style of past MDCAT papers — below are 12 of them with answers and explanations, and the full set of 50 questions is in the HighYield MDCAT QBank.

This chapter covers: Mendel's laws, alleles, dominance, sex-linkage, chromosomes, mutations and pedigree analysis.

Inheritance and Genetics MCQs with answers

Q1.When chromosomes uncoil, the nucleoli are reformed and two nuclei are the two poles of the cell; stage is known as

  • A.Prophase
  • B.Metaphase
  • C.Telophase
  • D.Anaphase
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Correct answer: C. Telophase

Telophase is the mitotic stage in which chromosomes uncoil, nucleoli reform, and two separate nuclei form at opposite poles of the cell.

Q2.During maternal mitosis, non-disjunction of autosomal chromosome pair results in the formation of an egg having 24 chromosomes in:

  • A.Klinefelter's Syndrome
  • B.Down's Syndrome
  • C.Turner's Syndrome
  • D.Jacob's Syndrome
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Correct answer: B. Down's Syndrome

Maternal non-disjunction of an autosomal pair, producing an egg with 24 chromosomes, is the usual origin of Down's syndrome.

Q3.Genetically engineered cells are introduced into bone marrow cells in the treatment of

  • A.Hypercholesterolemia
  • B.Severe Combined Immunodeficiency Syndrome (SCID)
  • C.Cystic Fibrosis
  • D.Coronary Artery Angioplasty
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Correct answer: B. Severe Combined Immunodeficiency Syndrome (SCID)

In gene therapy for Severe Combined Immunodeficiency Syndrome (SCID), genetically engineered cells carrying a functional ADA gene are introduced into the patient's bone marrow.

Q4.A technique in transgenic animals in which desired gene is inserted into the eggs of animal is called:

  • A.Embryonic Stem Cell mediated Transfer
  • B.Microinjection
  • C.Retro-virus mediated gene Transfer
  • D.Virus vectors
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Correct answer: B. Microinjection

Microinjection is the technique used in transgenic animals in which the desired gene is directly injected into a fertilized egg using a fine needle.

Q5.When the presence of a gene at one locus suppresses the effect of a gene at another locus, the phenomenon is called

  • A.Hypostasis
  • B.Pleiotropy
  • C.Epistasis
  • D.Epitropy
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Correct answer: C. Epistasis

Epistasis occurs when the presence of a particular gene at one locus suppresses or masks the phenotypic effect of a gene at another locus.

Q6.When a gene expresses the effects of a gene at another focus, this is known as

  • A.Epistasis
  • B.Co-dominance
  • C.Complete dominance
  • D.Mutation
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Correct answer: A. Epistasis

Epistasis is the phenomenon in which a gene at one locus masks or expresses over the effect of a gene at another locus.

Q7.A character determined by three alleles is:

  • A.Human skin colour
  • B.Human blood group
  • C.Human eye colour
  • D.Human Rh factor
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Correct answer: B. Human blood group

Human blood group (ABO system) is a trait determined by three different alleles (IA, IB and i) at a single locus, illustrating multiple allelism.

Q8.Position of gene on chromosome is called:

  • A.Allele
  • B.Genotype
  • C.Locus
  • D.Phenotype
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Correct answer: C. Locus

Locus is the physical position a gene or a factor occupies on the chromosome.

Q9.According to the Biogenetic Law of Ernst Haeckel:

  • A.There is survival of the fittest
  • B.There is use and disuse of organs
  • C.Phylogeny recapitulates ontogeny
  • D.Ontogeny recapitulates phylogeny
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Correct answer: D. Ontogeny recapitulates phylogeny

This concept, proposed by Ernst Haeckel, suggests that the development of an individual organism (ontogeny) follows the same sequence of evolutionary changes seen in the evolutionary history of the species (phylogeny). According to this idea, an organism goes through stages during its development that resemble the adult forms of its evolutionary ancestors.

Q10.Mode of Inheritance in humans can be traced through:

  • A.Experimental Mating
  • B.Chi Square Chart
  • C.Pedigree analysis
  • D.Probability analysis
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Correct answer: C. Pedigree analysis

Pedigree analysis is the most commonly used method to trace the mode of inheritance in humans. It involves the construction of a family tree or pedigree that tracks the occurrence of a trait through generations.

Q11.Which of the following increases genetic variation the most?

  • A.Cloning
  • B.Self-pollination
  • C.Crossing over
  • D.Asexual reproduction
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Correct answer: C. Crossing over

Crossing over produces new allele combinations during meiosis, greatly enhancing variation. Asexual methods do not increase variation.

Q12.In crossing over, the exchange of maternal and paternal chromatids occurs while homologous chromosomes are paired during:

  • A.Prophase meiosis I
  • B.Prophase meiosis II
  • C.Metaphase of meiosis I
  • D.Anaphase meiosis II
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Correct answer: A. Prophase meiosis I

Option A is correct. Crossing over occurs during prophase I of meiosis I, when homologous chromosomes pair up and exchange segments of their genetic material, leading to genetic variation in the offspring. In contrast, Option B is incorrect because prophase II occurs after the homologous chromosomes have been separated, and no crossing over takes place. Option C is also incorrect; during metaphase I, homologous chromosomes align but do not exchange genetic material. Lastly, Option D is incorrect as anaphase II focuses solely on the separation of sister chromatids, with no involvement of crossing over.

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