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NEET UG 2026 » NEET UG Study Material » Biology » Mutations
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Mutations

A mutation is a change in the DNA sequence that occurs in a cell. Infection by viruses, exposure to ionising radiation, exposure to substances known as mutagens, or faults in DNA copying during cell division are all examples of how mutations can occur in humans.

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Mutations are changes in the structure of our DNA base pairs produced by a variety of external factors including UV light or errors during DNA replication. Somatic mutations occur in body cells and are not transmitted on, but germline mutations occur in eggs and sperm and is not handed down to offspring.

Mutations

Mutations are necessary for evolution to take place because they are the source of all new genetic information or alleles in a species. Some mutations are advantageous to the creatures in which they occur, despite the fact that the majority of mutations have no impact on the organisms where they occur. A mutagen, on the other hand, is a material that can cause a permanent change in the physical structure of the DNA gene, so altering the genetic message.

The impact of a mutation may vary depending on where the genetic material’s sequence has been altered. Substitutions of a single base pair with the other, having no influence on protein sequence, are the simplest and most harmless. Insertion or deletion mutations, on the other hand, result in non-functional gene products. Long sections of DNA (or RNA if it is genetic material) can be inserted, inverted, deleted, duplicated, transposed, or translocated, resulting in mutations on a huge scale.

Types of Mutation

Depending on the cause of the mutation, its influence on the function of the gene product, or the type of alterations to the gene’s structure, mutations can be categorised in a variety of ways.

Mutagenic substances, like high-energy radiation or carcinogens, alter genetic material. The mistake rate in RNA or DNA replication machinery causes some mutations as a natural result.

Silent Mutation

Any alteration in DNA sequence that has no effect on amino acid sequence in the protein or the functions performed by a protein is referred to as a silent mutation. There is also no phenotypic indication that a mutation has occurred.

Nonsense Mutation

A stop codon is formed when the sequence of the base pairs changes as a result of a point mutation. As a result, the protein is either truncated or rendered useless.

Missense Mutation

A missense mutation occurs when a point mutation causes changes in the codon, which codes for a different amino acid.

Effects of Mutation

There are certain mutations which cannot be passed down to offspring. Somatic mutations occur inside the somatic cells and hence are referred to as such.

Germline mutations, on the other hand, can be passed down through generations and arise in reproductive cells.

Mutation’s Beneficial Effect

Several mutations lead to additional protein versions, which help organisms adapt to changes in their environment. As a result of this type of mutations, evolution happens.

Antibiotic-resistant bacteria are bacterium strains which, due to mutations in numerous bacteria, may survive in the presence of antibiotics.

A rare mutation found in the Italian people prevents them from atherosclerosis, which is a disorder where fatty deposits accumulate in blood arteries.

Effects of Mutations

Genetic illnesses can be caused by mutations in one or more genes. Cystic fibrosis is caused by mutation in one or more genes in such genetic disorder.

Cancer is another disease induced by abnormalities in genes involved the cell cycle.

Causes of Mutation

Genetic diversification occurs as a result of the mutation. Positive mutations are passed down across generations.

Genetic variation occurs as a result of the mutation. Positive mutations are passed down across generations.

For example, sickle cell anaemia is caused by a mutation in the haemoglobin gene. The RBCs take on a sickle form. This mutation protects against malaria in the African population.

Cancer is caused by a mutation in gene that controls cell division.

Internal Causes

The bulk of mutations develop when DNA copies improperly. Each of these mutations contribute to evolution. During cell division, DNA duplicates itself. When a copy of DNA isn’t perfect, this is considered as mutation as it differs from the original DNA in some way.

External Causes

When certain chemicals or radiations are used to break down DNA, hence causes the DNA to decompose. 

Virus Mutation

Viruses have the ability to evolve. They have the ability to alter their genetic structure. The virus might be more or less of a danger to the human host as a result of these modifications. As a result, virologists are interested in following the viral genome’s evolution.

The purpose of a virus infecting a host cell is to replicate itself. The replication of genetic material is the first step in the process. This procedure is particularly prone to mistakes in viral cells. Complex organisms use effective proof – reading systems to ensure high-fidelity reproduction.

A mutation occurs when the genetic material RNA or DNA of a biological entity or specific organism differs from the original normal or wild type version of the genome. It’s possible that the mutation is completely new, or that it’s happened previously.

Conclusion

A mutation is a change in an organism’s DNA at a specific location. It is a change in the nucleotide sequence of an organism’s genome. Different classification standards exist for mutations. Point mutations, structural mutations, and numerical mutations are the most prevalent. Mutations can come from a variety of sources, including natural biological processes and man-made mutagens. Mutations are frightening because they produce a variety of heritable disorders and can activate oncogenes, which can lead to cancer. Mutation, on the other hand, is the initial step in evolution since it creates additional DNA sequences for a given gene, resulting in new alleles.

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Frequently asked questions

Get answers to the most common queries related to the NEET UG Examination Preparation.

Define mutation.

Ans. Mutations are changes in the DNA base pair caused by numerous environmental variables such as UV exposure or re...Read full

Discuss the cause of mutation.

Ans.  Internal Cause The ...Read full

Discuss the effects of mutation.

Ans. There are a number of mutations which cannot be transmitted down to the next generation. Somatic mutations ari...Read full

Ans. Mutations are changes in the DNA base pair caused by numerous environmental variables such as UV exposure or replication errors. It has the ability to change its base-pair sequence. It’s referred to as a mutation. A mutation can change the way proteins are transcribed by the DNA. Cells can generally detect and repair mutation-induced damage before it becomes irreversible.

Ans. 

Internal Cause

The bulk of mutations develop when DNA copies improperly. Each of these mutations contribute to evolution. During cell division, DNA duplicates itself. When a copy of DNA isn’t perfect, it’s referred to as a mutation because it differs from the original DNA in some way.

External Cause 

The DNA breaks down when particular radiations or chemicals are utilised to break it down. UV exposure breaks the thymine dimers, causing DNA to change.

Ans. There are a number of mutations which cannot be transmitted down to the next generation. Somatic mutations arise when mutations develop in the somatic cells.

Mutations in the germline can be handed down across generations and can develop in reproductive cells.

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