| Literature DB >> 28237796 |
Fedor Kouzine1, Damian Wojtowicz2, Laura Baranello1, Arito Yamane3, Steevenson Nelson3, Wolfgang Resch3, Kyong-Rim Kieffer-Kwon3, Craig J Benham4, Rafael Casellas3, Teresa M Przytycka5, David Levens6.
Abstract
DNA in cells is predominantly B-form double helix. Though certain DNA sequences in vitro may fold into other structures, such as triplex, left-handed Z form, or quadruplex DNA, the stability and prevalence of these structures in vivo are not known. Here, using computational analysis of sequence motifs, RNA polymerase II binding data, and genome-wide potassium permanganate-dependent nuclease footprinting data, we map thousands of putative non-B DNA sites at high resolution in mouse B cells. Computational analysis associates these non-B DNAs with particular structures and indicates that they form at locations compatible with an involvement in gene regulation. Further analyses support the notion that non-B DNA structure formation influences the occupancy and positioning of nucleosomes in chromatin. These results suggest that non-B DNAs contribute to the control of a variety of critical cellular and organismal processes. Published by Elsevier Inc.Entities:
Keywords: DNA topology; H-DNA; SIDD; Z-DNA; chromatin; cruciform; non-B DNA; quadruplex; supercoiling; transcription
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Year: 2017 PMID: 28237796 PMCID: PMC7432990 DOI: 10.1016/j.cels.2017.01.013
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304