<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Txt>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE334nnn/GSE334998/suppl/GSE334998_Readme.txt</Txt><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE334nnn/GSE334998/suppl/GSE334998_FP_Pol2_bg_corrected.bw</Other><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE334nnn/GSE334998/suppl/GSE334998_TRI_Pol2_bg_corrected.bw</Other><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE334nnn/GSE334998/suppl/GSE334998_DMSO_PAF1_bg_corrected.bw</Other><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE334nnn/GSE334998/suppl/GSE334998_DMSO_Spt5_bg_corrected.bw</Other><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE334nnn/GSE334998/suppl/GSE334998_TRI_Spt5_bg_corrected.bw</Other><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE334nnn/GSE334998/suppl/GSE334998_FP_Spt5_bg_corrected.bw</Other><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE334nnn/GSE334998/suppl/GSE334998_FP_PAF1_bg_corrected.bw</Other><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE334nnn/GSE334998/</Other><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE334nnn/GSE334998/suppl/GSE334998_TRI_PAF1_bg_corrected.bw</Other><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE334nnn/GSE334998/suppl/GSE334998_DMSO_Pol2_bg_corrected.bw</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Drosophila melanogaster</species><gds_type>Genome binding/occupancy profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE334998</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcription machinery clustering by Integrator synchronizes histone gene expression</name><description>Numerous components of the transcription machinery, including RNA polymerase II (Pol II), accumulate in high-concentration clusters at gene promoters. Whether these clusters assemble on demand during transcription or constitute regulatory units remains unclear. Examining the Drosophila histone locus—where histone genes normally transcribe exclusively during S phase—we unexpectedly found large clusters containing non-chromatin-bound Pol II and elongation factors outside of S phase. When transcription activates during S phase, P-TEFb drives an accelerated turnover of the cluster components. Dispersion of clusters through depletion of the Integrator complex endonuclease module causes histone transcription to have a diminished S-phase peak and instead occur ectopically throughout the cell cycle. We propose that clusters constitute gate-keeping hubs that maintain a poised machinery pool, restricting gene activation to defined temporal windows.</description><dates><publication>2026/06/10</publication></dates><accession>GSE334998</accession><cross_references><GSM>GSM9803169</GSM><GSM>GSM9803168</GSM><GSM>GSM9803181</GSM><GSM>GSM9803180</GSM><GSM>GSM9803167</GSM><GSM>GSM9803166</GSM><GSM>GSM9803165</GSM><GSM>GSM9803164</GSM><GSM>GSM9803163</GSM><GSM>GSM9803162</GSM><GSM>GSM9803161</GSM><GSM>GSM9803160</GSM><GSM>GSM9803159</GSM><GSM>GSM9803158</GSM><GSM>GSM9803179</GSM><GSM>GSM9803157</GSM><GSM>GSM9803170</GSM><GSM>GSM9803178</GSM><GSM>GSM9803156</GSM><GSM>GSM9803155</GSM><GSM>GSM9803177</GSM><GSM>GSM9803176</GSM><GSM>GSM9803154</GSM><GSM>GSM9803175</GSM><GSM>GSM9803153</GSM><GSM>GSM9803152</GSM><GSM>GSM9803174</GSM><GSM>GSM9803173</GSM><GSM>GSM9803151</GSM><GSM>GSM9803172</GSM><GSM>GSM9803150</GSM><GSM>GSM9803171</GSM><GPL>22106</GPL><GSE>334998</GSE><taxon>Drosophila melanogaster</taxon></cross_references></HashMap>