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dc.contributor.authorBartas, Martin
dc.contributor.authorPetrovič, Michal
dc.contributor.authorBrázda, Václav
dc.contributor.authorTrenz, Oldřich
dc.contributor.authorĎurčanský, Aleš
dc.contributor.authorŠťastný, Jiří
dc.date.accessioned2025-08-12T02:03:09Z
dc.date.available2025-08-12T02:03:09Z
dc.date.issued2025
dc.identifier.issn0021-9258 Sherpa/RoMEO, JCR
dc.identifier.urihttps://repozitar.mendelu.cz/xmlui/handle/20.500.12698/2108
dc.description.abstractWith continuous advances in DNA sequencing methods, accessibility to high-quality genomic information for all living organisms is ever increasing. However, to interpret this information effectively and formulate hypotheses, users often require higher level programming skills. Therefore, the generation of web-based tools is becoming increasingly popular. CpG island regions in genomes are often found in gene promoters and are prone to DNA methylation; with their methylation status determining if a gene is expressed. Notably, understanding the biological impact of CpX modifications on genomic regulation is becoming increasingly important as these modifications have been associated with diseases such as cancer and neurodegeneration. However, there is currently no easy-to-use scalable tool to detect and quantify CpX islands in full genomes. We have developed a Java-based web server for CpX island analyses that benefits from the DNA Analyzer Web server environment and overcomes several limitations. For a pilot demonstration study, we selected a well-described model organism Drosophila melanogaster. Subsequent analysis of obtained CpX islands revealed several interesting and previously undescribed phenomena. One of them is the fact, that nearly half of long CpG islands were located on chromosome X, and that long CpA and CpT islands were significantly overrepresented at the subcentromeric regions of autosomes (chr2 and chr3) and also on chromosome Y. Wide genome overlays of predicted CpX islands revealed their co-occurrence with various (epi)genomics features comprising cytosine methylations, accessible chromatin, transposable elements, or binding of transcription factors and other proteins. CpX Hunter is freely available as a web tool at: https://bioinformatics.ibp.cz/#/analyse/cpgen
dc.format108537
dc.publisherAmerican Society for Biochemistry and Molecular Biology
dc.relation.ispartofJournal of Biological Chemistry
dc.relation.urihttps://doi.org/10.1016/j.jbc.2025.108537
dc.rightsCC BY 4.0
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectCpG islandsen
dc.subjectCpA islandsen
dc.subjectCpT islandsen
dc.subjectGenome analysesen
dc.subjectDinucleotideen
dc.subjectWeb serveren
dc.subjectDrosophilaen
dc.titleCpX Hunter web tool allows high-throughput identification of CpG, CpA, CpT, and CpC islands: A case study in Drosophila genomeen
dc.typeJ_ČLÁNEK
dc.date.updated2025-08-12T02:03:09Z
dc.description.versionOA
local.identifier.doi10.1016/j.jbc.2025.108537
local.identifier.scopus2-s2.0-105005253128
local.identifier.wos001498943500004
local.number6
local.volume301
local.identifier.obd43928418
local.identifier.e-issn1083-351X
dc.project.IDIGA-PEF-DP-23-033
dc.project.IDAnalýza vlastností písma na základě vztahu rozlišení a stupně písma.
dc.identifier.orcidTrenz, Oldřich 0000-0002-1260-590X
dc.identifier.orcidŠťastný, Jiří 0000-0003-3724-6357
local.contributor.affiliationPEF
dc.relation.funderMSM


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Except where otherwise noted, this item's license is described as CC BY 4.0