<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE283nnn/GSE283485/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE283485</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>G-quadruplexes regulate chromatin accessibility and gene expression in Bloom Syndrome [RNA-seq]</name><description>Bloom Syndrome (BS) is a recessive genetic disorder characterized by hyper-recombination and genome instability. It is caused by mutations in the conserved RecQ helicase gene, BLM, which acts to unwind various aberrant DNA structures. One such structure is DNA G-quadruplexes (G4s), which have broad regulatory functions. Despite previous association between putative G4-forming sequences and BS, it remains unclear what (dys)regulatory role, if any, endogenous G4 structures may play in BS. Here, we profiled chromatin accessibility and gene expression via ATAC-seq and RNA-seq and mapped endogenous G4 via ChIP-seq in wild-type (WT) vs. BS cell lines. We observed that in BS, differential G4 formation positively correlated with both differential chromatin accessibility and gene expression. To test the direct involvement of G4s in the molecular phenotypes in BS, we applied pyridostatin, a G4-stabilizing molecule, in WT cells and showed that G4 stabilization partially phenocopied BS. Additionally, data from a BS family showed that regions with increased chromatin accessibility in BS individuals were also enriched for G4-forming sequences. Our data showed that G4 formation promotes chromatin accessibility and gene expression; likely in BS, unresolved G4 increases focal chromatin accessibility, thereby upregulating gene expression. In summary, our results revealed a central role of G4 in the molecular etiology of BS and provide a new perspective on BLM’s regulatory function through G4s.</description><dates><publication>2026/04/10</publication></dates><accession>GSE283485</accession><cross_references><GSM>GSM8663327</GSM><GSM>GSM8663316</GSM><GSM>GSM8663317</GSM><GSM>GSM8663306</GSM><GSM>GSM8663328</GSM><GSM>GSM8663307</GSM><GSM>GSM8663329</GSM><GSM>GSM8663318</GSM><GSM>GSM8663319</GSM><GSM>GSM8663308</GSM><GSM>GSM8663312</GSM><GSM>GSM8663323</GSM><GSM>GSM8663324</GSM><GSM>GSM8663313</GSM><GSM>GSM8663314</GSM><GSM>GSM8663325</GSM><GSM>GSM8663315</GSM><GSM>GSM8663326</GSM><GSM>GSM8663320</GSM><GSM>GSM8663310</GSM><GSM>GSM8663321</GSM><GSM>GSM8663322</GSM><GSM>GSM8663311</GSM><GSM>GSM8663309</GSM><GPL>24676</GPL><GSE>283485</GSE><taxon>Homo sapiens</taxon><PMID>[41867784]</PMID></cross_references></HashMap>