<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>192(5)</volume><submitter>Keese AM</submitter><pubmed_abstract>The hyperthermophilic archaeon Pyrococcus furiosus grows optimally near 100 degrees C and undergoes a heat shock response at 105 degrees C, mediated at least in part by the heat shock regulator Phr. Genes encoding a small heat shock protein (HSP20) and a member of the AAA(+) ATPase are the only known targets of the regulator, but a genetic mutant of Phr has yet to be characterized. We describe here an alternative approach for the identification of the regulon of Phr based on cell-free transcription of fragmented chromosomal DNA in the presence or absence of the regulator and hybridization of in vitro RNA to P. furiosus whole-genome microarrays. Our results confirmed the phr, the hsp20, and the aaa(+) ATPase genes as targets of Phr and also identified six additional open reading frames, PF0</pubmed_abstract><journal>Journal of bacteriology</journal><pagination>1292-8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2820856</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Genome-wide identification of targets for the archaeal heat shock regulator phr by cell-free transcription of genomic DNA.</pubmed_title><pmcid>PMC2820856</pmcid><pubmed_authors>Adams MW</pubmed_authors><pubmed_authors>Schut GJ</pubmed_authors><pubmed_authors>Keese AM</pubmed_authors><pubmed_authors>Thomm M</pubmed_authors><pubmed_authors>Ouhammouch M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genome-wide identification of targets for the archaeal heat shock regulator phr by cell-free transcription of genomic DNA.</name><description>The hyperthermophilic archaeon Pyrococcus furiosus grows optimally near 100 degrees C and undergoes a heat shock response at 105 degrees C, mediated at least in part by the heat shock regulator Phr. Genes encoding a small heat shock protein (HSP20) and a member of the AAA(+) ATPase are the only known targets of the regulator, but a genetic mutant of Phr has yet to be characterized. We describe here an alternative approach for the identification of the regulon of Phr based on cell-free transcription of fragmented chromosomal DNA in the presence or absence of the regulator and hybridization of in vitro RNA to P. furiosus whole-genome microarrays. Our results confirmed the phr, the hsp20, and the aaa(+) ATPase genes as targets of Phr and also identified six additional open reading frames, PF0</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Mar</publication><modification>2025-04-26T04:19:48.057Z</modification><creation>2019-03-27T00:28:33Z</creation></dates><accession>S-EPMC2820856</accession><cross_references><pubmed>20023014</pubmed><doi>10.1128/JB.00924-09</doi><doi>10.1128/jb.00924-09</doi></cross_references></HashMap>