Introduction
Ever since childhood, the concept of mutations has sparked curiosity in many minds. Inspired by various films showcasing incredible abilities, the reality of mutations, however, is deeply rooted in genetics, posing fundamental questions about life itself. In this article, we will delve into the complexities of mutations, how they occur, the different types, and their implications for organisms, specifically humans.
What Are Mutations?
Mutations refer to changes in the genetic material of an organism, specifically alterations within nucleic acids like DNA and RNA. Consequently, every organism, including animals, plants, fungi, bacteria, and even viruses, is susceptible to mutations.
Types of Mutations
Mutations can be broadly categorized into two types:
- Gene Mutations: Changes that occur within specific genes affecting proteins that determine an organism's traits.
- Chromosomal Mutations: Alterations involving the structure or number of chromosomes.
Random Nature of Mutations
It's crucial to understand that mutations are random occurrences. They cannot be consciously induced, meaning organisms do not have the ability to will themselves to acquire a beneficial mutation. External factors such as exposure to certain chemicals or radiation and internal factors like errors in DNA replication can increase the likelihood of mutations.
Delving Deeper: Types of Gene Mutations
1. Substitution
This involves one base pair being replaced by another, potentially leading to functional changes in proteins.
2. Insertion
This occurs when one or more extra bases are added into the DNA sequence, which may disrupt the reading frame during protein synthesis.
3. Deletion
In deletion mutations, one or more bases are removed from the DNA sequence, leading to similar risks associated with frameshift mutations.
Frameshift Mutations
When insertions or deletions happen, the reading frame shifts, causing subsequent codons to change, potentially resulting in completely different amino acids. This can lead to significant functional changes in proteins, contributing to various genetic disorders.
Chromosomal Mutations
Chromosomal mutations involve larger structural changes in the chromosomes, including:
- Duplication: An extra copy of one or more genes.
- Deletion: Loss of genetic material, which can lead to significant effects depending on the genes affected.
- Inversion: A segment of the chromosome is reversed.
- Translocation: Genetic material is transferred between non-homologous chromosomes.
Vulnerable Stages
Mutations can happen during DNA replication, particularly during interphase. It is also important to consider meiosis in the production of gametes, where nondisjunction can result in gametes with too many or too few chromosomes.
Transmission of Mutations
Mutations can be hereditary, meaning they can pass from parent to offspring, especially when present in reproductive cells (sperm and eggs).
For instance, in organisms like fruit flies, studies of mutations offer great insights into genetics due to their short lifespans and fast reproduction rates.
Case Study: Sickle Cell Anemia
A notable example of gene mutations is sickle cell anemia, which arises from a mutation in the gene coding for hemoglobin. This mutation alters red blood cell shape, affecting oxygen transportation.
- Individuals with two copies of the mutated gene suffer from the disorder, while carriers with one mutated gene exhibit some resistance to malaria, showcasing the complex interplay of genetics and environment.
The Role of Genetic Counseling
As research in genetics evolves, the field is becoming increasingly significant. Genetic counselors play a crucial role in assisting families affected by genetic disorders, providing valuable information and support. For those interested in genetics and its applications, numerous career opportunities await.
Conclusion
Mutations are a fundamental element of genetics, influencing evolution and health across species. While they occur randomly, their impacts can be profound, leading to significant traits in organisms and hereditary diseases in humans. Understanding mutations not only enhances our knowledge of biology but also informs medical practices and genetic counseling. Stay curious and keep exploring the wonders of mutations!
Captions are on! Click CC at bottom right to turn off. Ever since I was a kid, I have been curious about mutations. I think certain movies may have had an impact; I used to imagine mutations with amazing abilities.
But, there was also a lot I didn’t understand. Let me explain. Many people understand that a mutation is a change of genetic material---more specifically
a change within a nucleic acid. RNA and DNA are both types of nucleic acids. Therefore, anything with RNA or DNA can have a mutation.
That means animals- and that definitely includes humans- also plants, fungi, protists, bacteria, Archeaa- they can all have mutations. Additionally, so can viruses.
Many mutations can be neutral in effect. You can see this codon codes for the amino acid leucine. But if it experiences this particular silent mutation, even though a base has been altered,
it still codes for leucine. It did not change the amino acid. Mutations can also be harmful or helpful.
But it’s important to understand that mutations are random. The organism can’t “will” itself to get a certain mutation. You can learn more about this in our natural selection video where we talk about how a
bacterium may already possess a helpful mutation that allows it to survive an antibiotic, but the bacterium didn’t “will” itself to mutate to get this certain mutation. Ok, so again, mutations are random.
But there can be factors that can make mutations more likely to occur. External factors like certain types of chemicals or excessive radiation or internal factors like an event that causes a problem with DNA replication in interphase.
During interphase, cells can replicate DNA before they divide. So let’s discuss some different types of mutations. We’ll start with gene mutations.
DNA makes up genes and genes can code for proteins that influence different traits. So when a mutation in DNA happens, which specifically means a change in one or more DNA bases, then different proteins can be produced which can affect an organism’s traits.
In this example, we have fruit fly DNA. Mutations could include substitution which means the wrong base is matched. Insertion, which means an extra base (or bases) are added in.
There is also deletion, which means a base is removed. Insertions and deletions have the potential to be especially dangerous. Why?
Remember in protein synthesis, how we talked about how bases are read in threes? Well if you add a base or remove a base, suddenly the number of bases total has changed. And if you read the bases in threes---depending on where it happened---- everything that is
read afterwards could be affected. We call this a frameshift mutation. If you look at this frameshift example here where a single base has been inserted, you
can see now how the following codons---which have 3 bases each---are now all affected as the reading frame has been shifted. This example shows how it can lead to many amino acid changes.
There are also chromosomal mutations. Remember that chromosomes are made up of DNA and protein----highly organized---and they have lots of genes on them.
The human chromosome number is 46 with 23 from an egg cell and 23 from a sperm cell. This type of fruit fly here, however, has 8 chromosomes so 4 came from an egg cell and 4 came from a sperm cell.
Some examples of chromosomal mutations include duplication, where extra copies of genes are generated. Deletion, where some of the genetic material breaks off.
Inversion, when a broken chromosome segment gets inversed (which means reversed) and put back on the chromosome. Or translocation when a fragment from one chromosome breaks off and attaches to another
chromosome. There’s more mutations than what we covered of course, but the idea is that there are many different kinds of changes that can happen.
If a mutation is going to happen, we already mentioned that there are especially vulnerable times such as during DNA replication but also there are other times too…like meiosis. In fruit flies and other animals, meiosis makes sperm and egg cells that can have half
the number of chromosomes as the organism. However, sometimes those chromosomes don’t separate completely. We call this nondisjunction.
This can result in an egg or sperm cell that has too many or too few chromosomes. It’s possible for a mutation to be passed down to an offspring. Consider a protist with a mutation.
Many protists reproduce asexually, and when they divide, the daughter cell can inherit the same mutation. A fruit fly, which reproduces sexually, can pass a mutation to its offspring if that mutation
is found in the genetic material of the sperm or egg cell. You may wonder why we’ve been mentioning fruit flies so much? Well, they’re AWESOME.
But, also, it turns out that fruit fly mutations---and how they are inherited---are frequently studied. We have some links in the video description for more info. These studied mutations can also occur in humans, and we’ll give a gene mutation example
of a substitution in the case of sickle cell anemia. First- a little background. Hemoglobin is a protein in your red blood cells that helps you carry oxygen.
But in the disorder sickle cell anemia, the gene that codes for hemoglobin is mutated. If you inherit two copies of this gene (one from each parent), you can have this disorder. This disorder can make it difficult for your red blood cells to carry oxygen because the
shape of the red blood cell is affected from this mutated hemoglobin protein. This can lead to anemia and other problems. While unfortunately there is not a cure for this disorder yet, the good news is that treatment
for this disorder has greatly improved. Another thing to mention, if an individual only inherits one copy of the mutated gene from one parent, they are a carrier but they don’t officially have the disease.
Usually they do not have symptoms. But those that are carriers appear to have a protective factor against malaria. Malaria is a disease caused by a protist that can be transmitted by mosquitoes.
These individuals can still get malaria, but their symptoms are often less severe. We should mention that studying mutations and genetic disorders is a large and important field right now.
Genetic counselors work to help families that may be affected by genetic disorders. If you have an interest in learning more about careers related to this topic, please check out some of our further reading suggestions in the description below.
Heads up!
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