Principles of inheritance and variation MCQ: The principles of inheritance and variation is a crucial subject that receives significant weight in competitive exams and is covered in the class 12 biology curriculum. The fundamental ideas of heredity and biological theories are explained in this chapter.
Students will study Mendel's rule of inheritance, mutation, Sex determination, incomplete dominance, the chromosomal theory of inheritance, and many other topics in this chapter. Following Mendel's research and contributions to the science of genetics, the concept of inheritance pattern was formed. This chapter offers insight into genetics, the core of contemporary biology.NEET 2025 Exam Important Links | |
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Q 1. Which of the following statements about aneuploidy is false?
Answer- Option (2) is correct.
Explanation: Non-disjunction of non-homologous chromosomes prevents aneuploidy from developing. Instead, it results from the homologous pair of chromosomes' non-disjunction. It causes the development of a gamete with an additional chromosome and a gamete without one chromosome in the other.
Q 2. Which of the following examples of aneuploidy is false?
Answer- Option (4) is correct.
Explanation: Aneuploidy does not occur in phenylketonuria. Aneuploid disorders include Down's syndrome, Klinefelter's syndrome, and Turner's syndrome; Down's and Klinefelter's show trisomy problems, whilst Turner's syndrome displays monosomic abnormalities.
An uncommon genetic condition known as phenylketonuria, or PKU, causes the body to accumulate phenylalanine, an amino acid. The phenylalanine hydroxylase (PAH) gene is altered in PKU. The enzyme required to degrade phenylalanine is produced in part because of this gene. When a person with PKU consumes protein-containing meals or aspartame, an artificial sweetener, a hazardous accumulation of phenylalanine can occur because this person lacks the enzyme required to break down phenylalanine. This may ultimately result in severe health issues.Q 3. Which of the following types of mutations occurs the most frequently?
Answer- Option (3) is correct.
Explanation: The most frequent sort of mutation is a forward mutation, in which the normal or wild type of gene transforms into a new genotype that may be dominant or recessive. A forward mutation is a genetic change from a wild-type to a mutant allele or the generation of a new mutation from a wild-type allele. New qualities in the population evolve as a result of the forward mutation.
Q 4. Which of the following chemicals can cause mutations in both replicating and non-replicating DNA?
Answer- Option (2) is correct.
Explanation: The chemical mutagen nitrous acid is mutagenic to both replicating and non-replicating DNA. Strong mutagens known as acridines can cause frameshift or gibberish mutations. Numerous compounds are mutagenic or capable of resulting in mutations.
A chemical mutagen that changes DNA's adenine bases into hypoxanthine bases is nitrous acid. Although adenine typically bases pairs with thymine during replication, the presence of hypoxanthine causes a base pairing with cytosine.Q 5. Which of the following assertions about ionizing radiation is false?
Answer- Option (4) is correct.
Explanation: Ionizing radiations, which induce chromosomal breakage, are to blame for several forms of cancer. The ionized cells exhibit aberrant cellular division. Additionally directly inversely correlated with radiation doses is the incidence of caused mutations. Ionizing radiation efficiently breaks up molecular interactions by dislodging electrons (ionization).
Such disturbance in living things can seriously harm cells and their genetic makeup. Even a single radiation track through a cell can cause a particular sort of DNA damage known as tightly spaced, numerous lesions that impair cellular DNA repair processes. While damage response mechanisms may be able to kill the majority of the cells suffering such radiation-induced damage, some cells are able to evade these pathways, proliferate, and eventually go through a malignant transformation, an important stage in the growth of cancer.Q 6. Which of the following claims about polyploidy is false?
Answer- Option (3) is correct.
Explanation: Polyploidy does not refer to chromosomal sets having less than two sets. After the telophase stage of cell division, cytokinesis does not take place in polyploidy settings, which causes a rise in the total number of chromosomes in an organism. Plants frequently exhibit polyploidy, which causes sterility in mammals.
Q 7. Which of the following techniques may be used to identify an inheritance pattern within a family?
Answer- Option (1) is correct.
Explanation: Pedigree analysis, a method of researching human genetic illnesses, may be used to track the pattern of inheritance of Mendelian disorders that are passed down to offspring in accordance with Mendelian principles.
Q 8. When is it possible for a woman to be colorblind?
Answer- Option (4) is correct.
Explanation: A girl can only be colorblind under two circumstances: i. when her father is colorblind and her mother carries the disease; ii. when both her father and mother are colorblind.
So, for a girl to be colorblind, her father must likewise be colorblind.Q 9. How many sickle cell genotypes are there in the population?
Answer- Option (3) is correct.
Explanation: In a population, sickle cell anemia can occur in three different genotypes. These are
Q 10. Which of the following assertions about alpha-thalassemia is false?
Answer- Option (2) is correct.
Explanation: Alpha-thalassemia is not passed down in a Mendelian-dominant manner. Instead, it is passed down by a Mendelian recessive mechanism. It is linked to the deletion of the 16p chromosome and involves the genes HBA1 and HBA2.
Q 11. Which of the following is a cause of thalassemia?
Answer- Option (1) is correct.
Explanation: A series of diseases collectively referred to as thalassemia are caused by a deficiency in the production of globin polypeptide in RBC. The excess of other globin chains that build up in our bodies and cause various illnesses result from the absence or diminished synthesis of one of the globin chains.
Q 12. Which of the following claims would be accurate if garden pea plants from Mendel's garden were sampled?
Answer- Option (1) is correct.
Explanation: Even when a recessive allele is present, the dominant allele can still express. Thus, dominant phenotypes are more prevalent. Because round seeds outnumber wrinkled seeds, they would be more common.
Q 13. Which of the following characteristics is not a result of Mendel's research?
Answer- Option (4) is correct.
Explanation: Mendel studied a huge sample of pea plants using the reliable scientific method as well as mathematical and statistical tools, making his findings unique in their field. He also established a trustworthy and respectable data source that may be used regularly to draw conclusions. Furthermore, his methods required taking care of the model organism at hand and were ethical even by today's standards.
Q 14. What process results in a genuine breeding line?
Answer- Option (1) is correct.
Explanation: The line that is homozygous for an allele is considered to be a genuine breeding line. Repeated self-pollination over many generations can accomplish this. As a result, features that would normally be suppressed by the presence of dominant alleles are revealed that are encoded by recessive alleles.
Q 15. Which of the following is not a pair of opposing characteristics Mendel studied?
Answer- Option (4) is correct.
Explanation: Mendel examined seven pairs of opposing features during his investigations. These comprised terminal flowers, full and constricted pods, axial and yellow pods, as well as green and yellow pods. Violet and white were the two floral colors that were examined.
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