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Z-DNA interaction proteins insights from ChIP-seq data

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68081707%3A_____%2F25%3A00641690" target="_blank" >RIV/68081707:_____/25:00641690 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216305:26310/26:0200528

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S0006291X25016262?pes=vor&utm_source=clarivate&getft_integrator=clarivate" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0006291X25016262?pes=vor&utm_source=clarivate&getft_integrator=clarivate</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.bbrc.2025.152910" target="_blank" >10.1016/j.bbrc.2025.152910</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Z-DNA interaction proteins insights from ChIP-seq data

  • Original language description

    Z-DNA is a noncanonical left-handed DNA conformation implicated in gene regulation and genome dynamics. Despite its biological relevance, the landscape of Z-DNA-binding proteins (ZBPs) in the human genome remains poorly characterized. In this study, we used the Z-Hunter algorithm to predict Z-DNA-forming sequences throughout the human genome. These predicted regions were then systematically overlaid with transcription factor (TF) binding profiles from the ChIP-Atlas database to identify proteins that co-localize with Z-DNA motifs. Our integrative analysis identified a diverse set of candidate ZBPs, including both known ZBP homologs and several TF, suggesting a broader regulatory role for Z-DNA in transcriptional control. This work provides a valuable resource for exploring the Z-DNA-protein interaction network and its potential implications for human health and disease.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10608 - Biochemistry and molecular biology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2025

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Biochemical and Biophysical Research Communications

  • ISSN

    0006-291X

  • e-ISSN

    1090-2104

  • Volume of the periodical

    790

  • Issue of the periodical within the volume

    NOV 19 2025

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    8

  • Pages from-to

    152910

  • UT code for WoS article

    001611185700002

  • EID of the result in the Scopus database

    2-s2.0-105020272957