<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/GSE318nnn/GSE318861/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Homo sapiens</species><gds_type>Genome binding/occupancy profiling by high throughput sequencing</gds_type><gds_type> Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE318861</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Quantitative analysis of Tat-dependent and host-driven HIV transcription by ChIP-seq and RNA-seq</name><description>HIV transcription is initiated by host transcriptional machinery prior to the production of the viral transactivator Tat, yet the magnitude and regulatory features of this Tat-independent transcriptional state remain poorly defined. In this study, we performed integrated chromatin and transcriptional profiling to quantitatively compare Tat-dependent and host-driven regulation of HIV and cellular gene expression. Jurkat T cells were infected with isogenic HIV constructs expressing functional Tat (TatWT) or lacking Tat expression (TatNull) and analyzed under non-stimulated and stimulated conditions. Genome-wide chromatin occupancy of Tat and transcriptional machinery was measured by ChIP-seq, and corresponding transcriptional output from both the HIV provirus and host genome was quantified by RNA sequencing. These datasets define the baseline host-driven transcriptional state of HIV in the absence of Tat and enable direct comparison with Tat-amplified transcriptional responses. Together, this integrated ChIP-seq and RNA-seq resource provides a quantitative framework for dissecting Tat-dependent and Tat-independent mechanisms of HIV transcriptional regulation in chromatin.</description><dates><publication>2026/07/01</publication></dates><accession>GSE318861</accession><cross_references><GSM>GSM9504893</GSM><GSM>GSM9504892</GSM><GSM>GSM9504895</GSM><GSM>GSM9504894</GSM><GSM>GSM9504930</GSM><GSM>GSM9504897</GSM><GSM>GSM9504896</GSM><GSM>GSM9504899</GSM><GSM>GSM9504898</GSM><GSM>GSM9504891</GSM><GSM>GSM9504890</GSM><GSM>GSM9504923</GSM><GSM>GSM9504889</GSM><GSM>GSM9504922</GSM><GSM>GSM9504925</GSM><GSM>GSM9504924</GSM><GSM>GSM9504927</GSM><GSM>GSM9504926</GSM><GSM>GSM9504929</GSM><GSM>GSM9504928</GSM><GSM>GSM9504882</GSM><GSM>GSM9504881</GSM><GSM>GSM9504884</GSM><GSM>GSM9504883</GSM><GSM>GSM9504886</GSM><GSM>GSM9504885</GSM><GSM>GSM9504921</GSM><GSM>GSM9504888</GSM><GSM>GSM9504887</GSM><GSM>GSM9504920</GSM><GSM>GSM9504880</GSM><GSM>GSM9504919</GSM><GSM>GSM9504912</GSM><GSM>GSM9504879</GSM><GSM>GSM9504911</GSM><GSM>GSM9504914</GSM><GSM>GSM9504913</GSM><GSM>GSM9504916</GSM><GSM>GSM9504915</GSM><GSM>GSM9504918</GSM><GSM>GSM9504917</GSM><GSM>GSM9504910</GSM><GSM>GSM9504909</GSM><GSM>GSM9504908</GSM><GSM>GSM9504901</GSM><GSM>GSM9504900</GSM><GSM>GSM9504903</GSM><GSM>GSM9504902</GSM><GSM>GSM9504905</GSM><GSM>GSM9504904</GSM><GSM>GSM9504907</GSM><GSM>GSM9504906</GSM><GPL>30173</GPL><GSE>318861</GSE><taxon>Homo sapiens</taxon><PMID>[42328785]</PMID></cross_references></HashMap>