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dc.contributor.authorVermeirssen, Vanessa
dc.contributor.authorDeplancke, Bart
dc.contributor.authorBarrasa, M. Inmaculada
dc.contributor.authorReece-Hoyes, John S.
dc.contributor.authorArda, H. Efsun
dc.contributor.authorGrove, Christian A.
dc.contributor.authorMartinez, Natalia Julia
dc.contributor.authorSequerra, Reynaldo
dc.contributor.authorDoucette-Stamm, Lynn
dc.contributor.authorBrent, Michael R.
dc.contributor.authorWalhout, Albertha J. M.
dc.date2022-08-11T08:08:58.000
dc.date.accessioned2022-08-23T16:14:05Z
dc.date.available2022-08-23T16:14:05Z
dc.date.issued2007-06-26
dc.date.submitted2008-09-22
dc.identifier.citationNat Methods. 2007 Aug;4(8):659-64. Epub 2007 Jun 24. <a href="http://dx.doi.org/10.1038/nmeth1063">Link to article on publisher's site</a>
dc.identifier.issn1548-7091 (Print)
dc.identifier.doi10.1038/nmeth1063
dc.identifier.pmid17589517
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33778
dc.description.abstractYeast one-hybrid (Y1H) assays provide a gene-centered method for the identification of interactions between gene promoters and regulatory transcription factors (TFs). To date, Y1H assays have involved library screens that are relatively expensive and laborious. We present two Y1H strategies that allow immediate prey identification: matrix assays that use an array of 755 individual Caenorhabditis elegans TFs, and smart-pool assays that use TF multiplexing. Both strategies simplify the Y1H pipeline and reduce the cost of protein-DNA interaction identification. We used a Steiner triple system (STS) to create smart pools of 4-25 TFs. Notably, we uniplexed a small number of highly connected TFs to allow efficient assay deconvolution. Both strategies outperform library screens in terms of coverage, confidence and throughput. These versatile strategies can be adapted both to TFs in other systems and, likely, to other biomolecules and assays as well.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=17589517&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1038/nmeth1063
dc.subjectAnimals; Caenorhabditis elegans; *Transcription, Genetic; Two-Hybrid System Techniques
dc.subjectGenetics and Genomics
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleMatrix and Steiner-triple-system smart pooling assays for high-performance transcription regulatory network mapping
dc.typeJournal Article
dc.source.journaltitleNature methods
dc.source.volume4
dc.source.issue8
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/439
dc.identifier.contextkey635314
html.description.abstract<p>Yeast one-hybrid (Y1H) assays provide a gene-centered method for the identification of interactions between gene promoters and regulatory transcription factors (TFs). To date, Y1H assays have involved library screens that are relatively expensive and laborious. We present two Y1H strategies that allow immediate prey identification: matrix assays that use an array of 755 individual Caenorhabditis elegans TFs, and smart-pool assays that use TF multiplexing. Both strategies simplify the Y1H pipeline and reduce the cost of protein-DNA interaction identification. We used a Steiner triple system (STS) to create smart pools of 4-25 TFs. Notably, we uniplexed a small number of highly connected TFs to allow efficient assay deconvolution. Both strategies outperform library screens in terms of coverage, confidence and throughput. These versatile strategies can be adapted both to TFs in other systems and, likely, to other biomolecules and assays as well.</p>
dc.identifier.submissionpathgsbs_sp/439
dc.contributor.departmentProgram in Molecular Medicine
dc.contributor.departmentProgram in Gene Function and Expression
dc.source.pages659-64
dc.contributor.studentH. Efsun Arda; Christian A. Grove


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