4.8 Article

Analysis of the mechanism of nucleosome survival during transcription

Journal

NUCLEIC ACIDS RESEARCH
Volume 42, Issue 3, Pages 1619-1627

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkt1120

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Funding

  1. National Institute of Allergy and Infectious Diseases (NIAID) [R21-AI090558]
  2. National Institutes of Health (NIH) [GM58650]
  3. Russian Foundation for Basic Research (RFBR) [12-04-31942]
  4. Intramural Research Program of the National Institutes of Health (NICHD)
  5. NIH [GM58650]

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Maintenance of nucleosomal structure in the cell nuclei is essential for cell viability, regulation of gene expression and normal aging. Our previous data identified a key intermediate (a small intranucleosomal DNA loop, circle divide-loop) that is likely required for nucleosome survival during transcription by RNA polymerase II (Pol II) through chromatin, and suggested that strong nucleosomal pausing guarantees efficient nucleosome survival. To evaluate these predictions, we analysed transcription through a nucleosome by different, structurally related RNA polymerases and mutant yeast Pol II having different histone-interacting surfaces that presumably stabilize the circle divide-loop. The height of the nucleosomal barrier to transcription and efficiency of nucleosome survival correlate with the net negative charges of the histone-interacting surfaces. Molecular modeling and analysis of Pol II-nucleosome intermediates by DNase I footprinting suggest that efficient circle divide-loop formation and nucleosome survival are mediated by electrostatic interactions between the largest subunit of Pol II and core histones.

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