Ch-4: Principles of Inheritance and Variation12 Questions
Before You Practice
Try each question on your own first. Use the Show Answer button only after you have selected your option, then read the explanation and revise the related concept from your chapter notes.
1. Gregor Mendel conducted his classical genetic experiments primarily on:
A. Garden pea (Pisum sativum)
B. Fruit fly (Drosophila)
C. Maize
D. Human pedigrees
Answer: A. Garden pea (Pisum sativum)
Explanation: Mendel chose the garden pea for his experiments due to its easily observable contrasting traits and short generation time.
2. Mendel's Law of Segregation states that:
A. The two alleles of a gene separate from each other during gamete formation
B. Genes located on different chromosomes assort independently
C. All traits observed are always dominant
D. Genetic traits always blend together in offspring
Answer: A. The two alleles of a gene separate from each other during gamete formation
Explanation: This law explains that each gamete receives only one allele of a gene pair, ensuring the two alleles segregate cleanly during meiosis.
3. In a dihybrid cross between two heterozygous parents, the typical phenotypic ratio observed in the F2 generation is:
A. 9:3:3:1
B. 3:1
C. 1:2:1
D. 1:1:1:1
Answer: A. 9:3:3:1
Explanation: This characteristic ratio arises from the independent assortment of two different gene pairs, each following Mendelian segregation.
4. A cross between an F1 heterozygote and a homozygous recessive parent is specifically called a:
A. Test cross
B. Dihybrid cross
C. Reciprocal cross
D. Back cross to the dominant parent
Answer: A. Test cross
Explanation: A test cross is used to determine the genotype of an individual showing a dominant phenotype, by crossing it with a homozygous recessive individual.
5. Sex determination in humans is primarily based on the presence of:
A. X and Y chromosomes
B. Only autosomes
C. Only X chromosomes
D. Hormone levels alone
Answer: A. X and Y chromosomes
Explanation: In humans, XX individuals typically develop as female and XY individuals typically develop as male, based on the sex chromosome combination.
6. Haemophilia, a well-known bleeding disorder, is an example of a:
A. Sex-linked recessive disorder
B. Autosomal dominant disorder
C. Autosomal recessive disorder
D. Y-linked disorder
Answer: A. Sex-linked recessive disorder
Explanation: The gene for haemophilia is located on the X chromosome and behaves as a recessive trait, making it more common in males.
7. Down's syndrome in humans is primarily caused by:
A. Trisomy of chromosome 21
B. Deletion of chromosome 21
C. Trisomy of the X chromosome
D. Monosomy of chromosome 21
Answer: A. Trisomy of chromosome 21
Explanation: Down's syndrome results from the presence of an extra copy of chromosome 21, giving affected individuals a total of 47 chromosomes.
8. Pedigree analysis is a technique primarily used to study the:
A. Inheritance pattern of a specific trait within a family
B. DNA sequence of an organism
C. Overall process of gamete formation
D. Physical structure of a chromosome
Answer: A. Inheritance pattern of a specific trait within a family
Explanation: By tracing a trait through several generations of a family, pedigree analysis helps determine whether it is dominant, recessive, or sex-linked.
9. Incomplete dominance results in a hybrid phenotype that is:
A. Intermediate between the two parental phenotypes
B. Identical to only one of the two parents
C. A blend that eventually reverses over generations
D. Never actually observed in nature
Answer: A. Intermediate between the two parental phenotypes
Explanation: In incomplete dominance, neither allele is fully dominant, resulting in offspring showing a blended intermediate trait.
10. The ABO blood group system in humans is a classic example of:
A. Multiple allelism
B. Sex-linked inheritance
C. Incomplete dominance exclusively
D. Polygenic inheritance exclusively
Answer: A. Multiple allelism
Explanation: The ABO blood group is controlled by three alleles (IA, IB, and i) present at a single gene locus, illustrating multiple allelism.
11. Linked genes are genes that are located:
A. On the same chromosome, and tend to be inherited together
B. On entirely different chromosomes
C. Only within mitochondrial DNA
D. Only on the sex chromosomes
Answer: A. On the same chromosome, and tend to be inherited together
Explanation: Since linked genes lie close together on the same chromosome, they tend to be transmitted together during inheritance, deviating from independent assortment.
12. A mutation is best described as a:
A. Sudden, heritable change occurring in the genetic material
B. Non-heritable change limited to the phenotype only
C. Change that can only result from crossing over
D. A type of dominant trait exclusively
Answer: A. Sudden, heritable change occurring in the genetic material
Explanation: Mutations are permanent alterations in the DNA sequence that can be passed on to offspring and serve as a source of genetic variation.