SOMATIC MUTATIONS - SCI & TECH

News: Somatic genetic variants: A genomic revolution hiding inside our cells

 

What's in the news?

       The human genome has 23 pairs of chromosomes, one inherited from each of our parents. The genome is the blueprint of our genetic makeup.

       The ovum and the sperm carry these blueprints from our parents. After fertilization, the combined single cell, with the 23 chromosomes, starts to divide, copying the genetic material over and over to nearly a trillion cells – which make up the human body.

 

Somatic Mutations:

       It is a genetic alteration acquired by a cell that can be passed to the progeny of the mutated cell in the course of cell division.

       It is influenced by the repeated copy-pasting of the genome i.e the rate of concurrence of somatic mutations will increase with age and the higher replacement of old cells by new cells i.e tissue turnover.

       It is also known as a driver mutation as it can sometimes make a cell fitter than others.

       They are distinct from germline mutations, which are inherited from parents and are present in every cell of an individual’s body.

       They occur due to various factors, such as exposure to environmental mutagens like radiation or chemicals, errors in DNA replication, and other cellular processes.

       They can affect the DNA sequence of specific genes, leading to changes in protein production or function.

 

Causes:

       The cause of mutation in Somatic cells due to errors made during DNA replication and repairing.

       Mutation can also cause contact with mutagens. It increases the mutation rate.

 

Significance:

       It plays a vital role in the human immunity system.

       By the mutation it has the ability to produce proteins through B and T cells.

 

Issues:

       The mutation of somatic cell can cause various types of disease.

       Cancer can occur by the mutation of somatic cells.

       Non-cancerous disease also occurs.

       Mosaicism within the germ line can be caused by mutations occurring in early

development.