It is possible to "reconstitute" nucleosomes by mixing DNA and his- tone octamers in 2M NaCl and then dialyzing to low salt. When such experiments were carried out using a specific 208-bp fragment of sea urchin DNA, the following results were obtained: Digestion of the product with micrococcal nuclease gave quantitative production of 146-bp DNA. Upon cleavage of this DNA with a restriction nucle- ase having a single site in the fragment, several sharp bands were obtained, with sizes as follows: 29 bp, 39 bp, 107 bp, 117 bp. How would you interpret these data in terms of nucleosome positioning on this DNA?

Biochemistry
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ISBN:9781319114671
Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
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Chapter1: Biochemistry: An Evolving Science
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It is possible to "reconstitute" nucleosomes by mixing DNA and his-
tone octamers in 2M NaCl and then dialyzing to low salt. When such
experiments were carried out using a specific 208-bp fragment of
sea urchin DNA, the following results were obtained: Digestion of
the product with micrococcal nuclease gave quantitative production
of 146-bp DNA. Upon cleavage of this DNA with a restriction nucle-
ase having a single site in the fragment, several sharp bands were
obtained, with sizes as follows: 29 bp, 39 bp, 107 bp, 117 bp. How
would you interpret these data in terms of nucleosome positioning
on this DNA?
Transcribed Image Text:It is possible to "reconstitute" nucleosomes by mixing DNA and his- tone octamers in 2M NaCl and then dialyzing to low salt. When such experiments were carried out using a specific 208-bp fragment of sea urchin DNA, the following results were obtained: Digestion of the product with micrococcal nuclease gave quantitative production of 146-bp DNA. Upon cleavage of this DNA with a restriction nucle- ase having a single site in the fragment, several sharp bands were obtained, with sizes as follows: 29 bp, 39 bp, 107 bp, 117 bp. How would you interpret these data in terms of nucleosome positioning on this DNA?
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