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Direct detection of linker DNA bending in defined-length oligomers of chromatin.
Author(s) -
Jiaqi Yao,
Peggy T. Lowary,
Jonathan Widom
Publication year - 1990
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.87.19.7603
Subject(s) - linker dna , linker , solenoid , chromatin , nucleosome , dna , biophysics , folding (dsp implementation) , chemistry , biology , biochemistry , physics , computer science , operating system , quantum mechanics , electrical engineering , engineering
Linker DNA, which connects between nucleosomes in chromatin, is short and, therefore, may be essentially straight and inflexible. We have carried out hydrodynamic and electron microscopic studies of dinucleosomes--fragments of chromatin containing just two nucleosomes--to test the ability of linker DNA to bend. We find that ionic conditions that stabilize the folding of long chromatin cause linker DNA in dinucleosomes to bend, bringing the two nucleosomes into contact. The results uphold a key prediction of the solenoid model of chromosome folding and suggest a mechanism by which proteins that are separated along the DNA can interact by direct contact.

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