Deletion (genetics)

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Genetic Deletions

Illustration of DNA replication, where deletion mutations can occur.

Overview

Genetic Deletions, also known as deletion mutations, deficiencies, or simply deletions, represent a type of mutation where a part of a chromosome or a sequence of DNA is left out during DNA replication. This genetic aberration can have significant implications for an organism's genetic makeup and overall health.

Definition and Significance

A deletion is marked by the symbol "Δ" and can range from the loss of a single nucleotide to large segments of a chromosome. These mutations are critical in the study of genetics and molecular biology, as they can lead to various genetic disorders and diseases.

Types of Deletions

Deletions can be categorized based on their size and impact:

  1. Single Base Deletion: The smallest type, involving the loss of a single nucleotide.
  2. Multi-base Deletion: Involves the deletion of multiple nucleotides.
  3. Chromosomal Deletion: Large-scale deletions that involve significant portions of a chromosome.

Mechanisms of Deletion Formation

The formation of deletions can occur through several mechanisms:

  1. Single Base Flipping: Occurs when a base in the template DNA flips, followed by strand slippage within the DNA polymerase active site.
  2. Non-homologous End Joining: A repair mechanism that can lead to deletions if ends of DNA strands are incorrectly joined.
  3. Homologous Recombination: Can result in deletions if crossing over during meiosis is unequal.
Illustrative diagram showing a chromosomal deletion.

Consequences of Deletions

The impact of deletions can vary:

Detection and Analysis

Techniques used to detect deletions include:

External Links

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