StudySmarter: Study help & AI tools
4.5 • +22k Ratings
More than 22 Million Downloads
Free
The phenotypes of many organisms are modifications from changes in the number of chromosomes in their cells, and sometimes even changes in only a part of them can be important. These numerical changes are usually described as variations in the organism's ploidy (-ploid is a Greek suffix that just means "number of chromosome sets"; hence, diploid would mean two sets of chromosomes).
Explore our app and discover over 50 million learning materials for free.
Lerne mit deinen Freunden und bleibe auf dem richtigen Kurs mit deinen persönlichen Lernstatistiken
Jetzt kostenlos anmeldenNie wieder prokastinieren mit unseren Lernerinnerungen.
Jetzt kostenlos anmeldenThe phenotypes of many organisms are modifications from changes in the number of chromosomes in their cells, and sometimes even changes in only a part of them can be important. These numerical changes are usually described as variations in the organism's ploidy (-ploid is a Greek suffix that just means "number of chromosome sets"; hence, diploid would mean two sets of chromosomes).
So, let's learn about polyploidy!
The definition of polyploidy is:
Polyploidy is defined as organisms carrying extra sets of chromosomes. That is, more than the normal two sets of homologous chromosomes.
For example, if an organism goes from being diploid (2n) to being tetraploid (4n), then it has undergone polyploidy.
The level of polyploidy is described in reference to a base number of chromosomes, usually indicated by n, which is defined as the number of chromosomes in one arrangement.
To get a better understanding of what polyploidy means, let's revise the concept of "genes". Genes are the blueprint for our biology.
Genes are small segments of DNA encoding proteins that could lead to the expression of a trait (for example, a gene for eye color) when passed from parent to offspring.
Genes are found in a fixed position (locus) on a chromosome. Each chromosome contains a linear molecule of DNA folded several times on itself, as well as ribonucleic acid (RNA) and proteins.
Now, organisms can have different forms of the same gene, called alleles. For example, G and g are different alleles of the G gene.
An organism is considered homozygous if it has two identical alleles for a given gene or trait.
An organism is considered heterozygous if it has two different alleles for a given gene or trait.
Diploid organisms contain a pair of chromosomes, where one chromosome was inherited from the mother, and the other chromosome from the father. Since these chromosomes are the same size, structure and contains the same genes, they are known as homologous chromosomes.
When a cell or organism has two sets of chromosomes (one inherited from the mother, and the other from the father), it is considered a diploid (2n) organism.
The conventional representation of the constitution of homologues within the nucleus is defined as a cell karyotype.
A karyotype shows an individual's complete set of chromosomes. It is created by taking a picture of a cell's chromosomes, cutting them out, and arranging them based on size, banding pattern, and centromere positions.
Except egg and sperm cells, which have only 23 chromosomes, all normal human cells contain 23 pairs of chromosomes, or 46 chromosomes in all.
When an egg and a sperm come together through fertilization, the offspring will have 46 chromosomes in total: 23 from the father and 23 from the mother.
Of the the 23 pairs of human chromosomes, 22 of them are called autosomes, which look the same in males and females. The 23rd pair, called the sex chromosomes, differs between males and females.
There are two sex chromosomes found in humans: X and Y.
Females have two X chromosomes.
Males have one X chromosome and one Y chromosome.
The karyotype below human chromosomes lined up in pairs.
During most of the cell cycle, chromosomes are dispersed in the nucleus and cannot be morphologically identified. Only when the cell divides do chromosomes become morphologically evident.
Now that we have this breakdown out of the way, let's hop back to the original track we were on. So, what happens if somehow an error occurs, changing the number of chromosomes or the overall process? We have what is called polyploidy!
There are two basic types of polyploidy (that are encountered in plants):
But before tackling polyploidy, you need to understand a little bit about how bodies make new cells. Plants are a different thing, but all human cells are diploid, so when gametes are created, they must be haploid or have only one set of chromosomes, so that the new organism can be diploid again.
However, during this process, sometimes something goes wrong. The most common occurrence is that a new gamete gets two copies of the chromosomes, which can happen when females produce eggs. When an egg with two sets of chromosomes fuses with a normal haploid sperm, the resulting cell has three sets of chromosomes, that is, it is triploid (3n).
Individuals with an entire supernumerary chromosomal set can be produced by artificial couplings or as a result of accidental events. Under certain circumstances triploid (3n), tetraploid (4n) or higher grade nuclei, can be formed. Each of these levels of polyploidy represents an increase in the number of haploid kits present.
First up is allopolyploidy.
Allopolyploidy happens when an organism has genetically distinct chromosomal sets from two or more different species.
In allopolyploidy, the different chromosomal assets are defined as homeologous, meaning that they are only partially homologous. Problems arise when an individual with a chromosomal mutation mates with an individual that has no chromosomal mutations, resulting in sterility.
Wheat is a hexaploid (6n) that results from three different diploid species, producing a stable hybrid called an allopolyploid.
It may happen, albeit rarely, that in some F1 hybrid plants, due to the absence of telophase, the doubling of chromosomes occurs; it follows that the cells of some tissues contain a chromosomal set which is the sum of the two parental sets.
The diploid arrangement, however, ensures that meiosis works regularly. The self-fertilization of these gametes gives rise to fertile plants, as they are produced by regular meiosis, the so-called allotetraploid plants, with two diploid sets.
Consequently, the allotetraploid plant behaves like a normal diploid plant. The doubling of genomes in such crosses leads to the loss of sterility, frequent in hybrids, and to the acquisition of fertility.
Now, let's look at autopolyploidy.
Autopolyploidy occurs when all the chromosomal sets present belong to the same species.
For example, let's say that you have two diploid (2n) plants of the same species that produce haploid (n) gametes; however, due to the lack of meiosis in one of the two parent plants, diploid gametes (2n) can be generated.
The crossing between diploid (2n) and haploid (1n) gametes produces a zygote triploid (3n), from which, in turn, haploid and diploid gametes will derive!
Meiosis is the process where a germ cell (reproductive cell precursor) divides into four haploid (n) daughter cells.
Following self-fertilization (2n × 2n), the autotetraploid zygote (4n) is obtained; the latter, like the other even-numbered autopolyploids, are more likely to be fertile because they can have regular meiosis!
Allopolyploidy is more common than autopolyploidy!
As we learned above, organisms with complete or normal arrangements of chromosomes are called euploids (derived from the Greek words meaning "well" and "once").
Organisms carrying extra sets of chromosomes are called polyploids (from the Greek words meaning "many" and "time") and the level of polyploidy is described with reference to a base number of chromosomes, usually indicated by "n" is defined as the number of chromosomes in an arrangement. Thus, diploids with two sets of chromosomes have 2n chromosomes, triploids with three have 3n arrangements, the tetraploids with 4 have 4n, and so on.
On the other hand, organisms with chromosomes, or segments of chromosomes, that are under- or overrepresented are called aneuploids.
Aneuploidy, from the Greek words meaning "not," "good" and "once"), is when an organism has an under- or overrepresented chromosome (or a segment of chromosome).
Trisomy and Monosomy are examples of aneuploidy. Trisomy means having 2n+1 chromosomes, while monosomy means having 2n-1 chromosomes.
Therefore, the main distinction between aneuploidy and polyploidy is that aneuploidy refers to the partial numerical change of the genome, usually a single chromosome, whereas polyploidy refers to the change of an entire set of chromosomes. Aneuploidy implies a genetic imbalance, while polyploidy does not.
Cytogenetics have also cataloged various types of structural changes in chromosomes.
Cytogenetics is the study of chromosomes and how they are inherited.
For example, a piece of a chromosome can be joined to another chromosome or a segment within a chromosome can be reversed. These structural changes are called rearrangements.
Because these rearrangements segregate irregularly during meiosis, they are often associated with aneuploidy.
Somatic cells have pairs of homologous chromosomes diploid (2n).
The germ cells that is the oocytes and the spermatozoa (gametes) are called haploid (n).
What organisms have polyploidy? Most often it is observed in the plant kingdom. Thousands of years of selective cultivation and plant breeding have resulted in the creation of fertile food plants, which are usually tetraploid and hexaploid.
Scientists have suggested that two-thirds of flowering plants are polyploid. Most ferns and herbs are polyploid, as are potatoes, apples, and strawberries.
Many succulents, as well as ornamental ones, those from seeds, and many fruit trees, are polyploid. Polyploidy is associated, typically, with infertility due to the difficulty of pairing of the chromosomes during meiosis.
The most visible effect of this condition is the lack of seeds in edible fruits, such as bananas (3n). The evolutionary success of polyploid plant species may result from the fact that polyploidy, like gene duplication, provides additional copies of genes; while one copy continues to perform its original function, the others can evolve by developing new functions!
Polyploid organisms can appear spontaneously or be generated by experimentally altering the spindle apparatus during cell division. This result is achieved with the use of colchicine, an alkaloid isolated from the seeds of autumnal Colchicum, which, added during plant cell culture, inhibits the formation of the spindle with consequent blockage of mitosis.
In this way, the absence of migration of chromosomes to the poles determines the formation of a tetraploid nucleus (4n). By repeating the same operation several times, polyploid nuclei are generated.
Among the most well-known polyploid plants are some varieties of ornamental plants with large flowers, such as hyacinths, tulips, and narcissus. In particular, triploids and tetraploids have characteristics of greater value than haploid or diploid plants, relating above all to the increase in cell volume, fruit, and stamens.
There are far fewer types of polyploid animals than plants. The exact reason for this is not fully known. Some scientists believe that this may be due to an increase in the complexity of the structure of animal organisms compared to plants.
Others suggest that polyploidy can interfere with gamete formation, cell division, or genome regulation. However, there are some exceptions. Examples of polyploidy in the animal kingdom are fish, reptiles, and insects.
Bananas are also an interesting example of polyploidy. Bananas are triploid and usually triploid organisms cannot reproduce, since they are sterile. This means that it is not possible to get banana seeds to sow more bananas. Therefore, farmers cut the shoots off the plant, before they produce fruit and finish their cycle, and plant a new generation.
What is autopolyploidy?
When a person possesses more than two sets of chromosomes, both derived from the same parental species
What is allopolyploidy?
When a person has more than two copies, but these copies are from distinct species.
What is polyploidy?
Polyploidy is defined as organisms carrying extra sets of chromosomes (from the Greek words meaning "many" and "time").
How is the level of polyploidy described?
by the letter n
What is aneuploidy?
Organisms in which a particular chromosome, or segment of it, is under or overrepresented are called aneuploid.
Which organism has the most polyploidy frequency?
Plants
Already have an account? Log in
Open in AppThe first learning app that truly has everything you need to ace your exams in one place
Sign up to highlight and take notes. It’s 100% free.
Save explanations to your personalised space and access them anytime, anywhere!
Sign up with Email Sign up with AppleBy signing up, you agree to the Terms and Conditions and the Privacy Policy of StudySmarter.
Already have an account? Log in