Problem 13
Question
Is this statement true or false? Inheriting three or more of each type of chromosome characteristic of the species results in a condition called polyploidy.
Step-by-Step Solution
Verified Answer
True.
1Step 1: Understanding chromosomal inheritance
In most species, chromosomes are inherited in pairs, one from each parent. This is the basis for the organism's diploid number. Typically, humans have 23 pairs of chromosomes, making for a total of 46.
2Step 2: Decoding polyploidy
Polyploidy is a condition in which an organism has more than two complete sets of chromosomes. While humans are diploid, polyploid organisms might have three (triploid), four (tetraploid), or more sets of each chromosome type.
3Step 3: Analyzing the given statement
The statement mentions inheriting three or more of each type of chromosome characteristic of the species. According to the definition of polyploidy, having more than two sets meets the criterion for polyploidy.
4Step 4: Assessing the statement
Given that inheriting three or more of each type of chromosome fits the definition of polyploidy, the statement must be true.
Key Concepts
Chromosome InheritanceDiploid NumberTriploid and Tetraploid
Chromosome Inheritance
In the realm of genetics, chromosome inheritance plays a pivotal role in determining the characteristics of an organism. Chromosomes are long strands of DNA that are found in the nucleus of cells, and they carry genes, which are the instructions for the development and functioning of all living things. In most animals and plants, this inheritance happens through a process where one complete set of chromosomes is inherited from each parent.
This results in what is called a diploid organism, meaning they have two sets of chromosomes. For example, in humans, there are 23 pairs of chromosomes, totaling 46.
This results in what is called a diploid organism, meaning they have two sets of chromosomes. For example, in humans, there are 23 pairs of chromosomes, totaling 46.
- One chromosome in each pair is inherited from the mother.
- The other is inherited from the father.
Diploid Number
The diploid number refers to the total number of chromosomes present in the cells of an organism when there are two sets - one from each parent. This property is designated as "2n," where "n" represents the number of different chromosomes in a single set. In humans, "n" is 23, giving a diploid number of \(2n = 46\).
Every living organism has a characteristic diploid number of chromosomes, which varies greatly among different species.
Every living organism has a characteristic diploid number of chromosomes, which varies greatly among different species.
- Mice, for instance, have a diploid number of 40.
- Frogs may have a diploid number of 24.
Triploid and Tetraploid
Polyploidy introduces more complexity to the genetic structure of an organism. In a typical diploid arrangement, an organism has two sets of chromosomes. However, polyploidy occurs when there are more than two sets.
In humans and many other animals, however, polyploidy is less common and often not viable due to complex development processes. Understanding this concept in plants gives insight into how genetic variations can contribute to survival and reproduction, showing how nature uses different mechanisms to thrive.
- When an organism has three sets of chromosomes, it is termed "triploid" (3n).
- With four sets, it is referred to as "tetraploid" (4n).
In humans and many other animals, however, polyploidy is less common and often not viable due to complex development processes. Understanding this concept in plants gives insight into how genetic variations can contribute to survival and reproduction, showing how nature uses different mechanisms to thrive.
Other exercises in this chapter
Problem 10
The SRY gene gives rise to the male phenotype in humans (Sections 10.3 and 14.4\()\). What do you think the inheritance pattern of SRY alleles is called?
View solution Problem 11
Nondisjunction may occur during __________ . a. mitosis b. meiosis b. meiosis d. both a and b
View solution Problem 14
Klinefelter syndrome \((\mathrm{XXY})\) can be easily diagnosed by __________ . a. pedigree analysis b. aneuploidy c. karyotyping d. phenotypic treatment
View solution Problem 15
Match the chromosome terms appropriately. ______polyploidy _______ deletion ______ aneuploidy _______ translocation _______ syndrome _______ transposable ______
View solution