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For a species with a diploid number of \(18,\) indicate how many chromosomes will be present in the somatic nuclei of individuals that are haploid, tetraploid, trisomic, and monosomic.

Short Answer

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Question: Determine the number of chromosomes present in the somatic nuclei of individuals with different ploidy and chromosomal abnormalities, given the diploid number is 18. Answer: The number of chromosomes in the somatic nuclei of the individuals are: - Haploid: 9 - Tetraploid: 36 - Trisomic: 19 - Monosomic: 17

Step by step solution

01

Find the chromosome number in haploid individuals

A haploid individual has only one set of chromosomes. Since the diploid number is 18, and it contains two sets of chromosomes, the haploid number is half of the diploid number. Therefore, the number of chromosomes in a haploid individual is: Chromosome number = \(\frac{Diploid\ number}{2}\) Chromosome number = \(\frac{18}{2}\) = \(9\)
02

Find the chromosome number in tetraploid individuals

A tetraploid individual has four sets of chromosomes. Since the diploid number is 18, and it contains two sets of chromosomes, the tetraploid number is twice the diploid number. Therefore, the number of chromosomes in a tetraploid individual is: Chromosome number = Tetraploid number * Diploid number Chromosome number = 2 * 18 = 36
03

Find the chromosome number in trisomic individuals

A trisomic individual has one extra chromosome in comparison to the normal diploid number. Therefore, the number of chromosomes in a trisomic individual is: Chromosome number = Diploid number + 1 Chromosome number = 18 + 1 = 19
04

Find the chromosome number in monosomic individuals

A monosomic individual has one less chromosome in comparison to the normal diploid number. Therefore, the number of chromosomes in a monosomic individual is: Chromosome number = Diploid number - 1 Chromosome number = 18 - 1 = 17 In conclusion, the number of chromosomes in the somatic nuclei of the individuals are: - Haploid: 9 - Tetraploid: 36 - Trisomic: 19 - Monosomic: 17

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Understanding Haploid
The term haploid refers to a cell that contains one complete set of chromosomes. Organisms use haploid cells during sexual reproduction; in humans, these are the sperm and egg cells. When the diploid number for a species is 18, this signifies that a diploid cell has 18 pairs of chromosomes, making for a total of 36 individual chromosomes. To find the haploid number, you would halve the diploid number:
\[ \text{Haploid number} = \frac{\text{Diploid number}}{2} \]
In this case, it results in:
\[ \text{Haploid number} = \frac{18}{2} = 9 \]
Therefore, a haploid cell for this species would have 9 chromosomes. Haploid cells are crucial for maintaining genetic diversity through meiosis, where they combine with another haploid cell to create a genetically unique diploid organism.
Tetraploid Organisms Explained
A tetraploid organism has four times the number of chromosomes than what is found in a haploid cell. This is a form of polyploidy, a condition where cells have more than two paired sets of chromosomes. For a species with a diploid number of 18, calculating the number of chromosomes in a tetraploid cell involves multiplying the diploid number by two:
\[ \text{Chromosome number} = 2 \times \text{Diploid number} \]
Thus:
\[ \text{Chromosome number} = 2 \times 18 = 36 \]
A tetraploid cell has 36 chromosomes. Tetraploidy can occur naturally, especially in the plant kingdom, and can lead to larger cell sizes, potentially influencing the organism's overall size and characteristics.
Understanding Trisomic Chromosome Variation
The term trisomic describes a condition where an organism or cell has an extra chromosome in addition to the normal diploid set. This adds a third copy of a particular chromosome, hence the prefix 'tri'. In a species with a diploid number of 18, a trisomic cell would carry one additional chromosome:
\[ \text{Chromosome number} = \text{Diploid number} + 1 \]
Applying this formula gives us:
\[ \text{Chromosome number} = 18 + 1 = 19 \]
Therefore, a trisomic individual would have 19 chromosomes in their somatic cells. Trisomy can cause genetic disorders, such as Down syndrome in humans, which is the result of an extra copy of chromosome 21.
Monosomic Cells in Genetics
Monosomy is a chromosomal abnormality where there is a missing chromosome from the normal diploid set. In a species that usually has 18 chromosomes in its diploid cells, a monosomic cell has one less:
\[ \text{Chromosome number} = \text{Diploid number} - 1 \]
Making the calculation,
\[ \text{Chromosome number} = 18 - 1 = 17 \]
A monosomic organism would have 17 chromosomes in each somatic cell. Monosomy can be detrimental to an organism's development and, in humans, is often fatal or causes developmental disorders, such as Turner syndrome, which involves having only one X chromosome.

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Most popular questions from this chapter

The primrose, Primula kewensis, has 36 chromosomes that are similar in appearance to the chromosomes in two related species, P. floribunda \((2 n=18)\) and \(P\). verticillata \((2 n=18) .\) How could P. kewensis arise from these species? How would you describe \(P\). kewensis in genetic terms?

Most cases of Turner syndrome are attributed to nondisjunction of one or more of the sex chromosomes during gametogenesis, from either the male or female parent. However, some females possess a rare form of Turner syndrome in which some of the cells of the body (somatic cells) lack an \(X\) chromosome, while other cells have the normal two X chromosomes. Often detected in blood and/or skin cells, such individuals with mosaic Turner syndrome may exhibit relatively mild symptoms. An individual may be specified as \(45, \mathrm{X}(20) / 46, \mathrm{XX}(80)\) if, for example, 20 percent of the cells examined were \(\mathrm{X}\) monosomic. How might mitotic events cause such mosaicism, and what parameter(s) would likely determine the percentages and distributions of X0 cells?

Contrast the genetic composition of gametes derived from tetrads of inversion heterozygotes where crossing over occurs within a paracentric versus a pericentric inversion.

Human adult hemoglobin is a tetramer containing two alpha (a) and two beta ( \(\beta\) ) polypeptide chains. The a gene cluster on chromosome 16 and the \(\beta\) gene cluster on chromosome 11 share amino acid similarities such that 61 of the amino acids of the \(\alpha\) -globin polypeptide (141 amino acids long) are shared in identical sequence with the \(\beta\) -globin polypeptide \((146\) amino acids long. How might one explain the existence of two polypeptides with partially shared function and structure on two different chromosomes?

Define these pairs of terms, and distinguish between them. aneuploidy/euploidy monosomy/trisomy Patau syndrome/Edwards syndrome autopolyploidy/allopolyploidy autotetraploid/amphidiploid paracentric inversion/pericentric inversion

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