The mutation is a common but not so common word among people. Of course, doctors, biologics, biochemists, higher secondary biology students and all those who are in or know about this field will be knowing this term. This isn’t just a simple thing as it seems. Changes caused due to mutation has the power to change the world, for good and for bad. The mere alterations occurring in our DNA brings novel origins and discoveries which are beyond one's imagination. So without further delay, let’s look into mutation.
Mutation definition Biology refers to a change in the nucleotide sequence of the genome of a living organism, virus, or extrachromosomal DNA. Viral genomes can be of DNA/RNA.
The change or alteration occurring in our DNA base sequences (A, C, G and T) is due to various environmental factors including Ultraviolet light and also due to errors caused when the DNA is copied.
RNA and both are types of nucleic acids, therefore, anything with RNA or DNA can have a mutation. It concludes that living organisms including animals, humans, plants, bacteria, fungi, protists and archaea can all have mutations. Also, viruses can have mutations. Many mutations are neutral in effect and can also be harmful as well as helpful in some manner (organisms can survive certain unfavorable conditions because of mutation).
(Image will be Uploaded soon)
The central dogma of molecular genetics involves the conversion of DNA into RNA (through transcription) and protein synthesis (through translation). Mutations make the protein synthesis go wrong during translation or mistakes in DNA are present that result in abnormalities in bodies in the form of some diseases like sickle cell anemia. So, the causes of mutation can be any of the below-mentioned points.
Mutations can be inherited from parents to a child.
Mutations are spontaneous, eg- DNA replication errors (internal factor), environmental factors and completely random reasons.
External factors such as certain types of chemicals or excessive radiation also cause mutations to occur.
After knowing the mutation definition and causes of mutation, let’s learn about different mutations and their types.
DNA makes up genes and genes can code for proteins, influencing various traits. However, not all genes code for proteins and not all genes are turned on.
Therefore, when a mutation in DNA occurs, it means a change in one or more DNA bases takes place, then different proteins are produced which affect an organism’s traits.
Example: A fruit fly's DNA faces mutations; it may include-
Substitution which means the wrong base is matched;
Insertion which means an extra-base or other bases are added in;
Deletion can occur which means a base is removed. So, the three types of gene mutations are substitution, insertion and deletion.
Insertions and deletions, discussed above, are known to have the potential to be especially dangerous. This is because if we add a base or remove a base, all of a sudden, the number of total bases change and every base that is read in three, everything that is read afterwards insertion/deletion could be affected. This is called frameshift mutation and it leads to many amino acid changes.
When mutations occur at the level of the chromosome, it is called chromosomal mutation. Chromosomes are made up of DNA and protein, are highly organized and have lots of genes on them. The human chromosome number is 46; 23 from an egg cell and 23 from a sperm cell. Similarly, the fruit fly has 8 chromosomes, 4 comes from an egg cell and 4 comes from the sperm cell.
Chromosomal Mutation Examples
Examples of chromosomal mutations are duplication, where extra copies of genes are generated.
Another is deletion, where some of the genetic material breaks off and inversion when a chromosome segment gets inverted (i.e. reversed) and put back on the chromosome.
The last one is translocation when a fragment from one chromosome breaks off and attaches to another chromosome.
During meiosis, in fruit flies and other animals, meiosis makes sperm and egg cells that can have half the number of chromosomes as the organism. And sometimes, those chromosomes don’t separate completely. It is called nondisjunction resulting in an egg or sperm cell that has too many or too few chromosomes.
Mutation can be passed down to an offspring; for example, a protist with mutation when undergoes asexual reproduction and division, the daughter cell can inherit the same mutation. These can be categorized as somatic mutations, which we will discuss later here.
Also, a fruit fly that reproduces sexually to pass a mutation to its offspring if that mutation is found in the genetic material of the sperm/egg cell. Frequent studies have been done to study fruit flies so these can be used to cite various examples for mutations.
Humans also pass down mutations to the offspring, for example, substitution occurring in the case of sickle cell anemia. Hemoglobin is a protein in your red blood cells that helps in carrying oxygen, however in sickle cell anemia, the gene coding for hemoglobin is mutated and if an offspring inherits two copies of this gene (one from each parent), it can have this disorder too. It is a condition where it is difficult for RBCs to carry oxygen because the shape of the RBC is affected by the mutated Hb protein. And in other cases, if an offspring gets one copy of a gene from one parent, it is only the carrier but not officially gets the disease.
Here, the cell that has acquired genetic alteration passes it to the progeny of the mutated cell during the extensive and complicated process of cell division. The mutation is basically occurring in the somatic cells of a multicellular organism rather than the germinating cell, ie; the egg and the sperm. That is what makes it different. Somatic mutations result from environment changers like Ultraviolet radiations and several other chemicals and artificial substances. The mutation affects all the cells from the mutated cell. These mutations can occur in the major part of the body of an organism or plant. It may showcase the mutation, or it may not showcase the mutation. This causes many diseases including cancer.
Because these gets transferred through somatic cells only, the mutation will not be passed to the next generation through sexual reproduction. If the mutation is to be multiplied, the mutated cell has to either go through cell division, as said earlier, I should be cloned.
Some of the somatic mutation examples include navel oranges and red apples.
In germinal mutation, the alteration in the germinal cells causes the mutation. Germ cells are the ones that give rise to gametes. So this mutation can be passed by sexual means. This can occur before fertilization and also during different stages of the zygote formation and its progression towards a child. If the mutation occurs before fertilization, then all the cells of that individual will be mutated. If the mutation occurs just after fertilization, it will be a gonosomal mutation. In the mutation developed sometime after fertilization, there will be a small set of cells either from germinating cells or somatic cells or both.
Genetic counselors work to help families that may be affected by genetic disorders; this cites the importance of studying mutations.
1. What is a mutation in genetics?
A mutation is a permanent change in the DNA sequence of a gene or chromosome. It can alter a single nucleotide or large segments of DNA, potentially affecting how a gene functions. Mutations may occur naturally during DNA replication or be caused by environmental factors like radiation or chemicals. Some mutations are harmless, some are beneficial, and others can lead to genetic disorders.
2. What causes genetic mutations?
Genetic mutations are caused by errors in DNA replication or exposure to environmental mutagens. Common causes include:
3. What are the main types of mutations?
The main types of mutations are gene mutations and chromosomal mutations.
4. How do mutations affect protein synthesis?
Mutations affect protein synthesis by altering the mRNA sequence transcribed from DNA, which can change the amino acid sequence of a protein. Depending on the mutation:
5. Are all mutations harmful?
No, not all mutations are harmful; mutations can be beneficial, neutral, or harmful.
6. What is the difference between a gene mutation and a chromosomal mutation?
A gene mutation affects the nucleotide sequence of a single gene, while a chromosomal mutation involves large segments of a chromosome.
7. Can mutations be inherited?
Yes, mutations can be inherited if they occur in germ cells (sperm or egg cells).
8. What is a point mutation?
A point mutation is a change in a single nucleotide base in the DNA sequence. It usually involves one base substitution, such as replacing adenine with guanine. Point mutations can be classified as:
9. How do mutations contribute to evolution?
Mutations contribute to evolution by creating genetic variation within populations.
10. What are examples of genetic disorders caused by mutations?
Genetic disorders caused by mutations include conditions resulting from changes in specific genes or chromosomes. Examples include: