So remember, chromosomal mutations refer to alteration in chromosome structure or the number of chromosomal copies. What we're discussing now is chromosomal copies. There are two types of chromosomal mutations, and we'll reference the copy number, and this is aberrant euploidy. And in this video, which we're not going to talk about, but this is working with the entire set of chromosomes. So if an organism has 40 sets of chromosomes, then there's going to be abnormal numbers of all 40. But what we're going to focus on is aneuploidy, and this changes the part of a single or a few chromosomes. So if the organism has 40 chromosome sets, then in an aneuploidy, only one or two of those chromosomes are going to have abnormal numbers. Aneuploidy refers to organisms found in some chromosomes, but not all of them, so not the whole set. And there are many different types. You can have trisomic, so I wrote 2n+1, so this is for diploid organisms. Right? So if you have 2n, that indicates diploid, but then you have one extra chromosome, plus one. An example of this is Down syndrome, right, where you have an extra chromosome of number 21, or Klinefelter's in humans, where you have that extra X chromosome, sex chromosome. Another term is monosomic, again, if it's diploid, 2n is diploid, but now it's minus one, so it has one less chromosome than a normal diploid organism. This is Turner Syndrome, which only has one X instead of two. If you're not familiar with these syndromes yet, don't worry about it. These are just examples if you are familiar with them. The really important thing to know is the terms and these numbers and what those numbers mean. Then you have nolesomic, which is 2n minus two for a diploid organism and can also refer to this as disomic, which is a haploid organism. Notice this is only n and not 2n's. So that suggests haploid minus one. So it's a haploid minus one chromosome. So it's actually lost an entire one of those chromosomes. Here's an example of what these look like: we have trisomic. You can see there are two diploids, which this organism is normally diploid, but they have this plus one, so they have this extra chromosome here. Here you have monosomic, so again, your diploid organisms, but it's minus one, so you have you're missing this chromosome here. Nolesomic is 2n-2, which might be harder to detect because here you have your two diploids. But because we're dealing with these organisms here, we know there's supposed to be a blue chromosome here, but there's not because both are missing, minus two. Disomic, now we're working with haploid. So, here are our normal half haploids, and we have plus one. So here is our plus one. So those are the different types of vocab words you're going to have to memorize. Now, here's nondisjunction. So nondisjunction is the failure of chromosomes to separate properly during division, and this is the cause of aneuploidy. It can occur in meiosis, which is most common during the formation of the gametes, but it can also occur in mitosis as well. If this mitosis is happening very early in development, like within the first few hours or days of development, this mitosis is occurring, and it just divides the chromosomes wrong. So, nondisjunction is the cause of these up here. And that's chromosomes not separating properly during or during division. Now, any aneuploid, so the ones we're talking about now, ones with only one chromosome added or missing, These are typically more abnormal than the type we talked about before, which are polyploids, and these are ones with the entire chromosome set. So all 40 chromosomes, for instance, have an extra copy. Whereas, aneuploids would be there, it'd still be 40, but it would just be 41. So why is that? Why is only having one chromosome extra so much worse than having 40 extra copies? Well, this actually has to do with a concept called gene balance. And this is the ratio of genes on one chromosome to genes on the other chromosome. So, if you normally have two chromosomes, and you have like three genes on each, And you have multiple chromosome sets. Right? Here we go. Now, it is less balanced to just get one extra copy here. Right? So now, I have nine copies of all of these genes, whereas I only have six of these. But if I got an extra chromosome here, then I have nine copies of these. And so, the balance of the number of genes on each chromosome is actually really important. So you want to have that balance. So the more so if you only have one extra copy, then all of your chromosomes have the same number of alleles, except for that one chromosome which has been added, and that gets you extra, and that really throws off your gene balance. Whereas, if you just have an extra copy of every chromosome, then the number of genes present in that cell is not the same, but it's equal across the chromosomes. And so you want that equal across the chromosome, even if that means having an extra copy of every chromosome or a less or missing a copy of every chromosome, because you want that gene balance. Whereas, if you have aneuploidy, where you only have one set, say, chromosome 9 that has an extra copy. Well, chromosome 9 now has extra alleles that none of the other chromosomes have, and that causes a more severe phenotype. And this has to do with gene dosage, and that's the relation between number of genes and the amount of gene product. So if, say we go back to, let me erase these circles here so we can see this better. So we go back to our original example here. We start out with two, we start out with the diploid organisms, these red chromosomes and the black chromosomes, and they each have the same number of alleles. Right? Same number of genes. Well, this means, say, that six gene copies are going to be produced, and six of this one. So we'll say chromosome number one and chromosome number two. So the red and the black chromosome will each produce six copies. But if you get an extra chromosome. Right? So if you get here, then that's going to mean how many are produced? It's going to mean nine are produced. And that means that you're going to have, more product than you should compared to every other gene. Right? Because six copies are still going to be produced down here. So you're going to get more of every gene on this chromosome, and that's going to give you a higher gene dosage.
6. Chromosomal Variation
Chromosomal Mutations: Aneuploidy
6. Chromosomal Variation
Chromosomal Mutations: Aneuploidy - Online Tutor, Practice Problems & Exam Prep
1
concept
Aneuploidy
Video duration:
9mPlay a video:
Video transcript
2
Problem
ProblemWhich of the following chromosomal mutations increases the amount of genetic material from only some chromosomes?
A
Aberrant Euploidy
B
Aneuploidy
C
Monoploidy
D
Tetraploidy
3
Problem
ProblemTrue or False:Aneuploids are more abnormal that polyploids
A
True
B
False
4
Problem
ProblemA species has 2n = 20. How many chromosomes will be found per mutant cell in an monosomic organism.
A
10
B
19
C
20
D
21
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PRACTICE PROBLEMS AND ACTIVITIES (36)
- In this chapter, we focused on extranuclear inheritance and how traits can be determined by genetic informatio...
- In this chapter, we have focused on chromosomal mutations resulting from a change in number or arrangement of ...
- In this chapter, we have focused on chromosomal mutations resulting from a change in number or arrangement of ...
- For a species with a diploid number of 18, indicate how many chromosomes will be present in the somatic nuclei...
- What evidence suggests that Down syndrome is more often the result of nondisjunction during oogenesis rather t...
- What evidence indicates that humans with aneuploid karyotypes occur at conception but are usually inviable?
- From the following list, identify the types of chromosome changes you expect to show phenotypic consequences.m...
- If the haploid number for a plant species is 4, how many chromosomes are found in a member of the species that...
- If the haploid number for a plant species is 4, how many chromosomes are found in a member of the species that...
- Describe how nondisjunction in human female gametes can give rise to Klinefelter and Turner syndrome offspring...
- The most common reason a physician might recommend that a woman have maternal serum screening and a karyotype ...
- The most common reason a physician might recommend that a woman have maternal serum screening and a karyotype ...
- When cows have twin calves of unlike sex (fraternal twins), the female twin is usually sterile and has masculi...
- An attached-X female fly, XXY (see the 'Insights and Solutions' box), expresses the recessive X-linked white-e...
- Assume that on rare occasions the attached X chromosomes in female gametes become unattached. Based on the par...
- What is a Barr body, and where is it found in a cell?
- Indicate the expected number of Barr bodies in interphase cells of individuals with Klinefelter syndrome; Turn...
- Drosophila may be monosomic for chromosome 4, yet remain fertile. Contrast the F₁ and F₂ results of the follow...
- Drosophila may be monosomic for chromosome 4, yet remain fertile. Contrast the F₁ and F₂ results of the follow...
- Define the Lyon hypothesis.
- Mendelian ratios are modified in crosses involving autotetraploids. Assume that one plant expresses the domina...
- Can the Lyon hypothesis be tested in a human female who is homozygous for one allele of the X-linked G6PD gene...
- In humans that are XX/XO mosaics, the phenotype is highly variable, ranging from females who have classic Turn...
- A plant breeder would like to develop a seedless variety of cucumber from two existing lines. Line A is a tetr...
- The woman in Problem 24 has had two miscarriages. She has come to you, an established genetic counselor, with ...
- In a recent cytogenetic study on 1021 cases of Down syndrome, 46 were the result of translocations, the most f...
- A boy with Klinefelter syndrome (47,XXY) is born to a mother who is phenotypically normal and a father who has...
- A boy with Klinefelter syndrome (47,XXY) is born to a mother who is phenotypically normal and a father who has...
- A boy with Klinefelter syndrome (47,XXY) is born to a mother who is phenotypically normal and a father who has...
- Most cases of Turner syndrome are attributed to nondisjunction of one or more of the sex chromosomes during ga...
- A 3-year-old child exhibited some early indication of Turner syndrome, which results from a 45,X chromosome co...
- A normal female is discovered with 45 chromosomes, one of which exhibits a Robertsonian translocation containi...
- For the following crosses, determine as accurately as possible the genotypes of each parent, the parent in who...
- For the following crosses, determine as accurately as possible the genotypes of each parent, the parent in who...
- For the following crosses, determine as accurately as possible the genotypes of each parent, the parent in who...
- For the following crosses, determine as accurately as possible the genotypes of each parent, the parent in who...