Question:

The recombination frequency between the genes a & c is 5%, b & c is 15%, b & d is 9%, a & b is 20%, c & d is 24% and a & d is 29%. What will be the sequence of these genes on a linear chromosome?

Updated On: May 2, 2025
  • a, d, b, c
  • d, b, a, c
  • a, b, c, d
  • a, c, b, d
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The Correct Option is D

Solution and Explanation

To determine the sequence of these genes on a linear chromosome, we use the given recombination frequencies, which are directly related to the physical distances between genes on the chromosome. Genes that are closer together on a chromosome have lower recombination frequencies, while genes further apart have higher frequencies. We'll follow these steps:
  1. Start by identifying the pair with the smallest recombination frequency, as they are closest together: Genes a & c have a recombination frequency of 5%.
  2. Next, we examine the recombination frequencies between the other genes and compare them to this initial pair to ascertain their positions:
    • The recombination frequency between b & c is 15%. Given that a & c are 5% apart, b should be placed further from c than a.
    • The recombination frequency between a & b is 20%. This suggests b is further from a, which confirms that b is between a & d. Hence, b should be placed beyond c from a.
    • The recombination frequency between c & d is 24%. This indicates that d is placed furthest from c compared to a, b, and c.
  3. From the above observations, the order of the genes starting from a is in line with these rates: a, c, b, d.
Thus, the correct sequence of the genes is a, c, b, d.
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Concepts Used:

Non-Mendelian Genetics

The term - non-mendelian inheritance refers to any pattern of heredity in which features do not separate according to Mendel's laws. These principles describe how features linked with single genes on chromosomes in the nucleus are passed down through generations.

Types of Non-Mendelian Inheritance

Codominance Inheritance

It is a form of incomplete dominance in which both alleles for the same feature are expressed in the heterozygote at the same time. For example, the MN blood types of humans.

Incomplete Dominance

In a heterozygote, the dominant allele does not always completely cover the phenotypic expression of the recessive gene, resulting in an intermediate phenotype which is referred to as "incomplete dominance”.