Question:

A man and a woman, who do not show any apparent signs of a certain inherited disease, have seven children (2 daughters and 5sons).Three of the sons suffer from the given disease but none of the daughters are affected. Which of the following mode of inheritance do you suggest for this disease?

Updated On: Apr 4, 2024
  • Autosomal dominant

  • Sex-linked dominant

  • Sex-limited recessive

  • Sex-linked recessive

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The Correct Option is D

Solution and Explanation

Based on the information provided, the most likely mode of inheritance for this disease is:
Sex-linked recessive
Here's the reasoning:
The man and woman do not show signs of the disease, which suggests they are carriers (heterozygous) for the disease gene.
Three out of the five sons are affected by the disease, while none of the daughters are affected. This pattern is consistent with X-linked recessive inheritance.
In X-linked recessive inheritance, the gene responsible for the disease is located on the X chromosome. Males have only one X chromosome, so if they inherit a copy of the disease gene, they will express the disease because there is no corresponding healthy allele on the Y chromosome to mask the effect. Females, on the other hand, have two X chromosomes, so they can be carriers without expressing the disease if they have one normal allele to compensate for the mutated one. This pattern explains why none of the daughters are affected (they received a normal X chromosome from the unaffected mother) and why three out of the five sons are affected (they inherited the X chromosome carrying the disease gene from their carrier mother).
So, based on the inheritance pattern observed in the family, X-linked recessive is the most likely mode of inheritance for this disease.

So, the correct option is (D): Sex-linked recessive

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Concepts Used:

Principles of Inheritance and Variation - Mutation

A Mutation is a change in the sequence of our DNA base pairs caused by numerous environmental stimuli such as UV light or mistakes during DNA replication. Germline mutations take place in the eggs and sperm and can be passed onto offspring, whereas somatic mutations take place in body cells and are not passed on.

Types of Mutations

There are three types of mutations, which are as follows:

Silent mutation

It refers to any change in DNA sequence that has no effect on the amino acid sequence in a protein or the functions that a protein performs. There is no phenotypic indication that a mutation has occurred.

Nonsense mutation

When there is a change in the sequence of base pairs due to a point mutation, that results in a stop codon. This leads to a protein that is either shortened or non-functional.

Missense mutation

A missense mutation occurs when a point mutation causes a change in the codon, which then codes for another amino acid.

The mutation is caused by the following factors:

Internal Causes

When DNA copies incorrectly, the majority of mutations occur. Evolution occurs as a result of all of these mutations. DNA makes a copy of itself during cell division. When a copy of DNA isn't flawless, it's called a mutation since it differs somewhat from the original DNA.

External Causes

When certain chemicals or radiations are used to break down DNA, it causes the DNA to break down. The thymine dimers are broken by UV radiation, resulting in altered DNA.