Match List-I with List-II:List-IList-II(A) Phenylketonuria(I) Incomplete dominance(B) Haemophilia(II) 9:3:3:1(C) Snapdragon(III) Pleiotropy(D) Dihybrid cross(IV) Sex-linked Choose the correct answer from the options given below:

Question

Prepp Team · Accepted Answer

Understanding Genetic Principles and Disorders

This question requires matching various genetic concepts, disorders, and phenomena with their appropriate descriptions or outcomes. Let's break down each item in List-I and find its corresponding match in List-II.

List-I	List-II
(A) Phenylketonuria	(I) Incomplete dominance
(B) Haemophilia	(II) 9:3:3:1
(C) Snapdragon	(III) Pleiotropy
(D) Dihybrid cross	(IV) Sex-linked

Analyzing Each Match

(A) Phenylketonuria and Pleiotropy

Phenylketonuria (PKU) is a metabolic disorder caused by a mutation in a single gene (the PAH gene). This single gene mutation affects the metabolism of phenylalanine, leading to a range of symptoms including intellectual disability, seizures, and behavioral problems if left untreated. This situation, where a single gene influences multiple distinct phenotypic traits, is known as pleiotropy.

Phenylketonuria (PKU): A genetic disorder.
Pleiotropy: The phenomenon where one gene has multiple effects on the phenotype.
Therefore, Phenylketonuria is an example of a condition caused by a gene exhibiting pleiotropy.

Thus, (A) matches with (III).

(B) Haemophilia and Sex-linked Inheritance

Haemophilia is a genetic disorder that impairs the body's ability to control blood clotting. It is primarily caused by a mutation on the X chromosome, which carries genes for clotting factors. Because males have only one X chromosome, a single mutated copy of the gene on the X chromosome will cause the disorder. Females, with two X chromosomes, are typically carriers unless they inherit two mutated copies (one from each parent). This pattern of inheritance, where the gene is located on a sex chromosome (like the X chromosome), is called sex-linked inheritance.

Haemophilia: A genetic blood disorder.
Sex-linked: Refers to genes located on sex chromosomes (X or Y) and their inheritance pattern.
Haemophilia is a classic example of an X-linked recessive disorder, which is a type of sex-linked inheritance.

Thus, (B) matches with (IV).

(C) Snapdragon and Incomplete Dominance

In genetics, dominance describes the relationship between alleles. In some cases, one allele does not completely dominate the other. In snapdragons (Antirrhinum majus), the alleles for flower color show incomplete dominance. When a red-flowered plant (genotype RR) is crossed with a white-flowered plant (genotype WW), the offspring (genotype RW) have pink flowers. The heterozygote phenotype is intermediate between the two homozygous phenotypes.

Snapdragon: A type of plant.
Incomplete dominance: A type of inheritance where the heterozygote phenotype is intermediate between the two homozygous phenotypes.
The flower color inheritance in snapdragons is a common example of incomplete dominance.

Thus, (C) matches with (I).

(D) Dihybrid Cross and 9:3:3:1 Ratio

A dihybrid cross involves tracking the inheritance of two different traits simultaneously. When two heterozygotes are crossed for two unlinked genes that exhibit complete dominance, the phenotypic ratio observed in the F₂ generation is typically 9:3:3:1. This ratio represents the proportion of individuals showing different combinations of the two traits (e.g., 9 showing both dominant traits, 3 showing dominant for one and recessive for the other, 3 showing recessive for the first and dominant for the second, and 1 showing both recessive traits).

Dihybrid cross: A genetic cross involving two different genes.
9:3:3:1: The classic phenotypic ratio observed in the F₂ generation of a dihybrid cross between heterozygotes when genes assort independently and show complete dominance.
The 9:3:3:1 ratio is a hallmark of Mendelian dihybrid inheritance under specific conditions.

Thus, (D) matches with (II).

Summary of Matches

Based on the analysis, the correct matches are:

(A) Phenylketonuria - (III) Pleiotropy
(B) Haemophilia - (IV) Sex-linked
(C) Snapdragon - (I) Incomplete dominance
(D) Dihybrid cross - (II) 9:3:3:1

This corresponds to the option (A)-(III), (B)-(IV), (C)-(I), (D)-(II).

Revision Table: Key Genetic Concepts

Concept	Description	Example
Pleiotropy	One gene influences multiple distinct phenotypic traits.	Phenylketonuria, Sickle cell anemia
Sex-linked inheritance	Inheritance pattern of genes located on sex chromosomes (X or Y).	Haemophilia, Red-green color blindness
Incomplete dominance	Heterozygote phenotype is intermediate between homozygous phenotypes.	Flower color in Snapdragon, Coat color in Andalusian chickens
Dihybrid cross	Genetic cross involving two traits.	Cross between peas differing in seed shape and color (Mendel's experiments)
9:3:3:1 ratio	Phenotypic ratio in F₂ generation of a dihybrid cross between heterozygotes (independent assortment, complete dominance).	Mendel's dihybrid crosses (e.g., pea shape and color)

Additional Information: Expanding on Genetic Inheritance

Understanding these fundamental concepts is crucial for grasping how traits are passed from one generation to the next. Genetics is a vast field, and these examples illustrate different patterns of inheritance beyond simple dominant-recessive relationships.

Alleles: Different forms of a gene.
Genotype: The genetic makeup of an organism (the combination of alleles).
Phenotype: The observable characteristics of an organism, resulting from the genotype and environmental influences.
Homozygous: Having two identical alleles for a gene (e.g., RR or WW).
Heterozygous: Having two different alleles for a gene (e.g., RW).
While the 9:3:3:1 ratio is typical for a dihybrid cross with independent assortment and complete dominance, other interactions between genes (like epistasis) can lead to modified dihybrid ratios.
Sex-linked disorders often show different frequencies in males and females due to the difference in sex chromosomes.

Studying specific examples like Phenylketonuria, Haemophilia, and Snapdragon helps solidify the understanding of abstract genetic principles like pleiotropy, sex-linkage, and incomplete dominance.

Prepp Team · Answer

(A)-(IV), (B)-(III), (C)-(I), (D)-(II)

Prepp Team · Answer

(A)-(IV), (B)-(II), (C)-(I), (D)-(III)

Prepp Team · Answer

(A)-(I), (B)-(III), (C)-(II), (D)-(IV)

List-I	List-II
(A) Down's Syndrome	(I) Absence of a copy of X chromosome
(B) Klinefelter's Syndrome	(II) Presence of additional copy of X chromosome
(C) Turner's Syndrome	(III) Mutation of X chromosome
(D) Colour blindness	(IV) Trisomy of 21st chromosome