top of page
Search

Everything you need to know about Genetic Mutation

You may heard of this term "mutation" in your biology class, a documentary on DNA or even a Youtube video. This blog post will discuss all about genetic mutations.


What is a Mutation?


A gene mutation is a permanent change in the DNA sequence that makes up a gene that varies from the sequence seen in other humans. Mutations can vary in size from a single DNA building block (base pair) to a large portion of a chromosome that contains several genes.


We must first determine if biological processes capable of reproduction are heritable; precisely, certain mutations affect only the human that bears them, while others affect all of the carrier organism's offspring and descendants. To have an effect on an organism's descendants, mutations must arise in cells that generate the next generation, and they must also affect the next generation's descendants. Mutations must develop in cells that contain the next generation and affect the genetic material in order to affect an organism's descendants. Finally, the interaction between hereditary genes and environmental pressures results in species richness.


While there are several different kinds of molecular modifications, the term "mutation" usually refers to one that affects the nucleic acids. These nucleic acids are the building blocks of DNA in cellular cells, and they are the building blocks of DNA or RNA in viruses.

DNA and RNA may be thought of as substances that store the information needed for an organism's reproduction in a long-term memory. While this article focuses on DNA mutations, we should bear in mind that RNA is subject to the same mutation powers.


Types of Mutations


The molecular aspects of how DNA and the whole genome are structured are closely related to the response to this issue. Point mutations, in which only one base pair is transformed into another, are the smallest mutations. Another type of mutation is a non synonymous mutation, which involves the alteration of an amino acid sequence. Such mutations cause a protein to be generated in a certain way or to be terminated prematurely.


Here is an informative that explains exactly what the types are


Effects


Each cell relies on thousands of proteins to do their jobs in the right positions at the right times in order to work properly. Gene mutations may often inhibit one or more of these proteins from functioning properly. A mutation may cause a protein to fail or go missing completely by altering the instructions for producing it in a gene. A mutation can interrupt normal growth or induce a medical disorder as it affects a protein that plays a vital role in the body. A genetic disease is an illness caused by mutations in one or more genes. Gene defects can be so serious that they block an embryo from surviving to birth in some cases. These mutations occur in genes that are critical for growth, and they often interrupt an embryo's development in its early stages. These mutations are incompatible with life because they have such severe consequences.


It's necessary to remember that genes don't cause disease; rather, mutations that cause a gene to act incorrectly cause genetic abnormalities. When someone gets “the cystic fibrosis gene,” An example, Sickle cell disease is caused by a mutation in the hemoglobin-Beta gene found on chromosome 11. Hemoglobin transports oxygen from the lungs to other parts of the body. Red blood cells with normal hemoglobin (hemoglobin-A) are smooth and round and glide through blood vessels.


Hope you all learned about genetic mutation. Stay Safe!


References


  • nature.com

  • medlineplus.gov

  • genome.gov


 
 
 

Comments


© 2020 by VFAT.

 821 Sainte Croix Ave, Saint-Laurent, Quebec H4L 3X9

Room D-105

Tel: 514-744-7500

  • Instagram
  • White Facebook Icon
  • White Twitter Icon
bottom of page