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Ch. 5 - Chromosome Mapping in Eukaryotes

Chapter 5, Problem 24

Traditional gene mapping has been applied successfully to a variety of organisms including yeast, fungi, maize, and Drosophila. However, human gene mapping has only recently shared a similar spotlight. What factors have delayed the application of traditional gene-mapping techniques in humans?

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Hi everyone. Let's look at our next question. It says bloom syndrome is characterized by pre natal and post natal retardation of growth, great sensitivity of the facial skin to the sun immune deficiency and abnormal behavior patterns, It is caused by a mutation in the blm gene located on chromosome 15. Which of the following is elevated in Bloom Syndrome. Well, the BLM gene we can recall is involved in the synthesis of the pro a hell a case protein. And as we can recall from learning about DNA replication, um this is unwinds the double helix as part of the DNA replication process. So the BLM mutation of LI L. M. Gene causes problems with the DNA replication. In particular, it causes an increase in the exchange of material from sister chroma tides. And it's thought that perhaps the reason of this is that this exchange is in response to access D. N. A damage that's occurred during DNA replication. And since those healing cases are such an important part of that DNA replication process, they sort of help to stabilize the entire process. So the disruption to the replication process results in increased DNA damage and the body sort of tries to repair that by having increased exchange of material between the sister chroma tights. So let's look at our answer choices here and we see that choice a right away is frequency of sister chromatic exchange and that is our correct answer. Um interestingly it also increases the amount of recombination. So exchange of material between uh the paired chromosomes from the two parents. So not only exchange between the sister chroma tides, but between the two different chromosomes from the two different parents. So, involved in both of those similar processes. We'll just take a quick look at our other answer choices. Choice B says the number of genes in the chromosomes. Well, this doesn't change there the same number of genes. You just have more frequent exchange of materials. Choice ceases the number of non functioning genes. Again, no effect on that. Um And Choice D. The D. N. A content in the chromosome. Uh No, that's not what it cause. It doesn't increase the DNA content. It just causes an increase in the amount of exchange of material between sister chroma ticks. So, again, which the following is elevated in bloom syndrome. Choice. A frequency of sister chromatic exchange. See you in the next video.
Related Practice
Textbook Question
An organism of the genotype AaBbCc was testcrossed to a triply recessive organism (aabbcc). The genotypes of the progeny are presented in the following table. 20 AaBbCc 20 AaBbcc 20 aabbCc 20 aabbcc 5 AabbCc 5 Aabbcc 5 aaBbCc 5 aaBbcc What can you conclude from the actual data about the location of the three genes in relation to one another?

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Textbook Question
Based on our discussion of the potential inaccuracy of mapping (see Figure 5.12), would you revise your answer to Problem 22? If so, how?
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Textbook Question
How do we know that in humans the X chromosomes play no role in human sex determination, while the Y chromosome causes maleness and its absence causes femaleness? Why are many expected crossover phenotypes missing? Can any of these loci be mapped from the data given here? If so, determine map distances.
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Textbook Question
In a certain plant, fruit is either red or yellow, and fruit shape is either oval or long. Red and oval are the dominant traits. Two plants, both heterozygous for these traits, were testcrossed, with the following results. Determine the location of the genes relative to one another and the genotypes of the two parental plants.
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Textbook Question
Two plants in a cross were each heterozygous for two gene pairs (Ab/aB) whose loci are linked and 25 mu apart. Assuming that crossing over occurs during the formation of both male and female gametes and that the A and B alleles are dominant, determine the phenotypic ratio of their offspring.
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Textbook Question
A number of human–mouse somatic cell hybrid clones were examined for the expression of specific human genes and the presence of human chromosomes. The results are summarized in the following table. Assign each gene to the chromosome on which it is located.
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