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How can genetic mutations be inherited from one generation to the next?
How can genetic mutations be inherited from one generation to the next?-February 2024
Feb 18, 2026 6:53 AM

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Definition: How can genetic mutations be inherited from one generation to the next?

Genetic mutations are changes in the DNA sequence that can be inherited from one generation to the next. These mutations can occur spontaneously or be caused by environmental factors such as radiation or chemicals. Inherited genetic mutations can be passed down from parents to their offspring through two main mechanisms: germline mutations and somatic mutations.

Germline Mutations

Germline mutations are genetic changes that occur in the cells that give rise to eggs and sperm, known as germ cells. These mutations can be present in every cell of an individual’s body and can be passed on to their offspring. Germline mutations can be inherited from one or both parents and can result in genetic disorders or an increased risk of developing certain diseases.

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Somatic Mutations

Somatic mutations, on the other hand, occur in the cells of the body that are not involved in reproduction, known as somatic cells. These mutations are not passed on to offspring as they are not present in the germline cells. Somatic mutations can arise during an individual’s lifetime due to various factors such as exposure to carcinogens or errors in DNA replication. These mutations can lead to the development of cancer or other diseases, but they are not inherited by future generations.

Mechanisms of Inheritance

The inheritance of genetic mutations follows different patterns depending on the type of mutation and the specific genes involved. Some mutations are inherited in an autosomal dominant manner, where a single copy of the mutated gene is sufficient to cause the disorder. In this case, an affected individual has a 50% chance of passing the mutation to each of their offspring.

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Other mutations are inherited in an autosomal recessive manner, where two copies of the mutated gene are required to cause the disorder. In this case, both parents are carriers of the mutation but do not show any symptoms. Each child of carrier parents has a 25% chance of inheriting two copies of the mutated gene and developing the disorder.

X-linked inheritance is another mechanism where the mutation is located on the X chromosome. This type of inheritance affects males more frequently than females, as males have only one X chromosome. If a male inherits the mutated gene, he will likely develop the disorder. Females, on the other hand, need to inherit two copies of the mutated gene to be affected.

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In conclusion, genetic mutations can be inherited from one generation to the next through germline mutations, which are present in the reproductive cells, or somatic mutations, which occur in non-reproductive cells. The inheritance patterns of these mutations depend on various factors, including the type of mutation and the genes involved.

Keywords: mutations, inherited, genetic, germline, somatic, inheritance, mutation, mutated, parents

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