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Describe intragenic complementation and the concept of cistron.

Introduction

In classical genetics, the gene was viewed as a single, indivisible unit of function. However, with the advancement of molecular biology, researchers discovered that even within a gene, different mutations can affect different functions. This led to the discovery of concepts like intragenic complementation and the cistron.

Intragenic Complementation

Definition

Intragenic complementation refers to the phenomenon where two different mutant alleles of the same gene, when present together in a heterozygous condition, can restore partial or full function of the gene product.

How It Works

Example

Consider a gene coding for a dimeric enzyme. Mutation A affects domain 1, and Mutation B affects domain 2. Alone, each produces a non-functional subunit. However, in a heterozygote (A/B), each mutation provides a functional copy of one domain. Together, they form a partially functional enzyme.

Significance

Concept of Cistron

Definition

A cistron is a section of DNA that codes for a single polypeptide chain. In simple terms, it is a gene in functional terms. The concept was introduced by Seymour Benzer.

Key Features

Difference Between Gene and Cistron

Relationship Between Intragenic Complementation and Cistron

Conclusion

Both intragenic complementation and the concept of cistron deepen our understanding of gene structure and function. While cistron defines the functional unit of DNA, intragenic complementation reveals the modular nature of proteins and the complexity within a single gene.

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