<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rong-Mullins X</submitter><funding>NHGRI NIH HHS</funding><pagination>607-619</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5919752</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(2)</volume><pubmed_abstract>Cellular metabolism can change the potency of a chemical's tumorigenicity. 4-nitroquinoline-1-oxide (4NQO) is a tumorigenic drug widely used on animal models for cancer research. Polymorphisms of the transcription factor Yrr1 confer different levels of resistance to 4NQO in &lt;i>Saccharomyces cerevisiae&lt;/i> To study how different Yrr1 alleles regulate gene expression leading to resistance, transcriptomes of three isogenic &lt;i>S&lt;/i>&lt;i>cerevisiae&lt;/i> strains carrying different Yrr1 alleles were profiled via RNA sequencing (RNA-Seq) and chromatin immunoprecipitation coupled with sequencing (ChIP-Seq) in the presence and absence of 4NQO. In response to 4NQO, all alleles of Yrr1 drove the expression of &lt;i>SNQ2&lt;/i> (a multidrug transporter), which was highest in the presence of 4NQO resistance-conf</pubmed_abstract><journal>G3 (Bethesda, Md.)</journal><pubmed_title>Transcriptional Profiling of &lt;i>Saccharomyces cerevisiae&lt;/i> Reveals the Impact of Variation of a Single Transcription Factor on Differential Gene Expression in 4NQO, Fermentable, and Nonfermentable Carbon Sources.</pubmed_title><pmcid>PMC5919752</pmcid><funding_grant_id>T32 HG000044</funding_grant_id><pubmed_authors>Summers M</pubmed_authors><pubmed_authors>Rong-Mullins X</pubmed_authors><pubmed_authors>Ayers MC</pubmed_authors><pubmed_authors>Gallagher JEG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcriptional Profiling of &lt;i>Saccharomyces cerevisiae&lt;/i> Reveals the Impact of Variation of a Single Transcription Factor on Differential Gene Expression in 4NQO, Fermentable, and Nonfermentable Carbon Sources.</name><description>Cellular metabolism can change the potency of a chemical's tumorigenicity. 4-nitroquinoline-1-oxide (4NQO) is a tumorigenic drug widely used on animal models for cancer research. Polymorphisms of the transcription factor Yrr1 confer different levels of resistance to 4NQO in &lt;i>Saccharomyces cerevisiae&lt;/i> To study how different Yrr1 alleles regulate gene expression leading to resistance, transcriptomes of three isogenic &lt;i>S&lt;/i>&lt;i>cerevisiae&lt;/i> strains carrying different Yrr1 alleles were profiled via RNA sequencing (RNA-Seq) and chromatin immunoprecipitation coupled with sequencing (ChIP-Seq) in the presence and absence of 4NQO. In response to 4NQO, all alleles of Yrr1 drove the expression of &lt;i>SNQ2&lt;/i> (a multidrug transporter), which was highest in the presence of 4NQO resistance-conf</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Feb</publication><modification>2026-05-01T19:45:10.363Z</modification><creation>2019-03-26T23:33:47Z</creation></dates><accession>S-EPMC5919752</accession><cross_references><pubmed>29208650</pubmed><doi>10.1534/g3.117.300138</doi></cross_references></HashMap>