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Ch. 10 - Eukaryotic Chromosome Abnormalities and Molecular Organization
Sanders - Genetic Analysis: An Integrated Approach 3rd Edition
Sanders3rd EditionGenetic Analysis: An Integrated ApproachISBN: 9780135564172Not the one you use?Change textbook
Chapter 10, Problem 27c

Genomic DNA from the nematode worm Caenorhabditis elegans is organized by nucleosomes in the manner typical of eukaryotic genomes, with 145 bp encircling each nucleosome and approximately 55 bp in linker DNA. When C. elegans chromatin is carefully isolated, stripped of nonhistone proteins, and placed in an appropriate buffer, the chromatin decondenses to the 10-nm fiber structure. Suppose researchers mix a sample of 10-nm–fiber chromatin with a large amount of the enzyme DNase I that randomly cleaves DNA in regions not protected by bound protein. Next, they remove the nucleosomes, separate the DNA fragments by gel electrophoresis, and stain all the DNA fragments in the gel.
How do the expected results support the 10-nm–fiber model of chromatin?

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Step 1: Understand the structure of chromatin in the 10-nm fiber model. Chromatin in this model consists of nucleosomes, which are DNA segments wrapped around histone proteins, and linker DNA, which connects adjacent nucleosomes. Each nucleosome protects approximately 145 base pairs (bp) of DNA, while the linker DNA is exposed and consists of approximately 55 bp.
Step 2: Recognize the role of DNase I in the experiment. DNase I is an enzyme that randomly cleaves DNA in regions not protected by bound proteins. In this case, it will preferentially cleave the exposed linker DNA while leaving the DNA wrapped around nucleosomes intact.
Step 3: Predict the outcome of DNase I treatment. After DNase I cleaves the linker DNA, the nucleosome-protected DNA fragments (approximately 145 bp) will remain intact. These fragments will be separated from the cleaved linker DNA during the subsequent steps of the experiment.
Step 4: Analyze the results of gel electrophoresis. When the DNA fragments are separated by size using gel electrophoresis, the nucleosome-protected DNA fragments will appear as a distinct band corresponding to approximately 145 bp. This supports the 10-nm fiber model, as it demonstrates that nucleosomes protect specific regions of DNA while leaving linker DNA exposed.
Step 5: Conclude how the results support the 10-nm fiber model. The presence of a consistent band of 145 bp DNA fragments in the gel indicates that nucleosomes are regularly spaced and protect specific regions of DNA, consistent with the organization of chromatin in the 10-nm fiber model.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Nucleosome Structure

Nucleosomes are the fundamental units of chromatin, consisting of DNA wrapped around a core of histone proteins. Each nucleosome typically contains about 145 base pairs of DNA, which is crucial for packaging the DNA into a compact structure. Understanding nucleosome organization is essential for interpreting how DNA is protected from enzymatic cleavage and how chromatin structure influences gene expression.
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Chromosome Structure

10-nm Fiber Model

The 10-nm fiber, also known as 'beads on a string,' represents the initial level of chromatin organization where nucleosomes are spaced along the DNA. This model illustrates how DNA is organized in a less condensed form, allowing for accessibility to transcription factors and enzymes. Analyzing the results of DNase I treatment helps confirm the presence of this structure by showing which regions of DNA are protected by nucleosomes.
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DNase I Cleavage

DNase I is an enzyme that cleaves DNA at sites that are not protected by bound proteins, such as histones in nucleosomes. When chromatin is treated with DNase I, the resulting DNA fragments can be analyzed to determine which regions were accessible and which were shielded by nucleosomes. The pattern of cleavage provides insights into the organization of chromatin and supports the 10-nm fiber model by demonstrating the protective role of nucleosomes.
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Related Practice
Textbook Question

DNase I cuts DNA that is not protected by bound proteins but is unable to cut DNA that is complexed with proteins. Human DNA is isolated, stripped of its nonhistone proteins, and mixed with DNase I. Samples are removed after 30 minutes, 1 hour, and 4 hours and run separately in gel electrophoresis. The resulting gel is stained to make all DNA fragments in it visible, and the results are shown in the figure. DNA fragment sizes in base pairs (bp) are estimated by the scale to the left of the gel. Draw a conclusion about the organization of chromatin in the human genome from this gel.

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Textbook Question

Genomic DNA from the nematode worm Caenorhabditis elegans is organized by nucleosomes in the manner typical of eukaryotic genomes, with 145 bp encircling each nucleosome and approximately 55 bp in linker DNA. When C. elegans chromatin is carefully isolated, stripped of nonhistone proteins, and placed in an appropriate buffer, the chromatin decondenses to the 10-nm fiber structure. Suppose researchers mix a sample of 10-nm–fiber chromatin with a large amount of the enzyme DNase I that randomly cleaves DNA in regions not protected by bound protein. Next, they remove the nucleosomes, separate the DNA fragments by gel electrophoresis, and stain all the DNA fragments in the gel.

Approximately what range of DNA fragment sizes do you expect to see in the stained electrophoresis gel? How many bands will be visible on the gel?

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Textbook Question

Genomic DNA from the nematode worm Caenorhabditis elegans is organized by nucleosomes in the manner typical of eukaryotic genomes, with 145 bp encircling each nucleosome and approximately 55 bp in linker DNA. When C. elegans chromatin is carefully isolated, stripped of nonhistone proteins, and placed in an appropriate buffer, the chromatin decondenses to the 10-nm fiber structure. Suppose researchers mix a sample of 10-nm–fiber chromatin with a large amount of the enzyme DNase I that randomly cleaves DNA in regions not protected by bound protein. Next, they remove the nucleosomes, separate the DNA fragments by gel electrophoresis, and stain all the DNA fragments in the gel.

Explain the origin of DNA fragments seen in the gel.

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Textbook Question

A small population of deer living on an isolated island is separated for many generations from a mainland deer population. The populations retain the same number of chromosomes but hybrids are infertile. One chromosome (shown here) has a different banding pattern in the island population than in the mainland population.

Describe how the banding pattern of the island population chromosome most likely evolved from the mainland chromosome. What term or terms describe the difference between these chromosomes?

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Textbook Question

A small population of deer living on an isolated island is separated for many generations from a mainland deer population. The populations retain the same number of chromosomes but hybrids are infertile. One chromosome (shown here) has a different banding pattern in the island population than in the mainland population.

Draw the synapsis of these homologs during prophase I in hybrids produced from the cross of mainland with island deer.

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Textbook Question

A small population of deer living on an isolated island is separated for many generations from a mainland deer population. The populations retain the same number of chromosomes but hybrids are infertile. One chromosome (shown here) has a different banding pattern in the island population than in the mainland population.

In a mainland–island hybrid deer, recombination takes place in band q1 of the homologous chromosomes. Draw the gametes that result from this event.

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