SELMAP - SELEX affinity landscape MAPping of transcription factor binding sites using integrated microfluidics
Transcription factors (TFs) alter gene expression in response to changes in the environment through sequence-specific interactions with the DNA. These interactions are best portrayed as a landscape of TF binding affinities. Current methods to study sequence-specific binding preferences suffer from l...
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creator | Chen, Dana Orenstein, Yaron Golodnitsky, Rada Pellach, Michal Avrahami, Dorit Wachtel, Chaim Ovadia-Shochat, Avital Shir-Shapira, Hila Kedmi, Adi Juven-Gershon, Tamar Shamir, Ron Gerber, Doron |
description | Transcription factors (TFs) alter gene expression in response to changes in the environment through sequence-specific interactions with the DNA. These interactions are best portrayed as a landscape of TF binding affinities. Current methods to study sequence-specific binding preferences suffer from limited dynamic range, sequence bias, lack of specificity and limited throughput. We have developed a microfluidic-based device for SELEX Affinity Landscape MAPping (SELMAP) of TF binding, which allows high-throughput measurement of 16 proteins in parallel. We used it to measure the relative affinities of Pho4, AtERF2 and Btd full-length proteins to millions of different DNA binding sites, and detected both high and low-affinity interactions in equilibrium conditions, generating a comprehensive landscape of the relative TF affinities to all possible DNA 6-mers, and even DNA10-mers with increased sequencing depth. Low quantities of both the TFs and DNA oligomers were sufficient for obtaining high-quality results, significantly reducing experimental costs. SELMAP allows in-depth screening of hundreds of TFs, and provides a means for better understanding of the regulatory processes that govern gene expression. |
doi_str_mv | 10.1038/srep33351 |
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These interactions are best portrayed as a landscape of TF binding affinities. Current methods to study sequence-specific binding preferences suffer from limited dynamic range, sequence bias, lack of specificity and limited throughput. We have developed a microfluidic-based device for SELEX Affinity Landscape MAPping (SELMAP) of TF binding, which allows high-throughput measurement of 16 proteins in parallel. We used it to measure the relative affinities of Pho4, AtERF2 and Btd full-length proteins to millions of different DNA binding sites, and detected both high and low-affinity interactions in equilibrium conditions, generating a comprehensive landscape of the relative TF affinities to all possible DNA 6-mers, and even DNA10-mers with increased sequencing depth. Low quantities of both the TFs and DNA oligomers were sufficient for obtaining high-quality results, significantly reducing experimental costs. SELMAP allows in-depth screening of hundreds of TFs, and provides a means for better understanding of the regulatory processes that govern gene expression.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep33351</identifier><identifier>PMID: 27628341</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>49/62 ; 631/1647 ; 631/61/191 ; Affinity ; Binding sites ; Deoxyribonucleic acid ; DNA ; DNA sequencing ; Environmental changes ; Gene expression ; Humanities and Social Sciences ; Microfluidics ; multidisciplinary ; Nucleotide sequence ; Peptide mapping ; Science ; Transcription factors</subject><ispartof>Scientific reports, 2016-09, Vol.6 (1), p.33351-33351, Article 33351</ispartof><rights>The Author(s) 2016</rights><rights>Copyright Nature Publishing Group Sep 2016</rights><rights>Copyright © 2016, The Author(s) 2016 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-ecf0cd64c23a687fb1de5ca7a6e509674dd5d217333218215612a71a4ec1ac643</citedby><cites>FETCH-LOGICAL-c438t-ecf0cd64c23a687fb1de5ca7a6e509674dd5d217333218215612a71a4ec1ac643</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5024299/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5024299/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27903,27904,41099,42168,51554,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27628341$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Dana</creatorcontrib><creatorcontrib>Orenstein, Yaron</creatorcontrib><creatorcontrib>Golodnitsky, Rada</creatorcontrib><creatorcontrib>Pellach, Michal</creatorcontrib><creatorcontrib>Avrahami, Dorit</creatorcontrib><creatorcontrib>Wachtel, Chaim</creatorcontrib><creatorcontrib>Ovadia-Shochat, Avital</creatorcontrib><creatorcontrib>Shir-Shapira, Hila</creatorcontrib><creatorcontrib>Kedmi, Adi</creatorcontrib><creatorcontrib>Juven-Gershon, Tamar</creatorcontrib><creatorcontrib>Shamir, Ron</creatorcontrib><creatorcontrib>Gerber, Doron</creatorcontrib><title>SELMAP - SELEX affinity landscape MAPping of transcription factor binding sites using integrated microfluidics</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Transcription factors (TFs) alter gene expression in response to changes in the environment through sequence-specific interactions with the DNA. These interactions are best portrayed as a landscape of TF binding affinities. Current methods to study sequence-specific binding preferences suffer from limited dynamic range, sequence bias, lack of specificity and limited throughput. We have developed a microfluidic-based device for SELEX Affinity Landscape MAPping (SELMAP) of TF binding, which allows high-throughput measurement of 16 proteins in parallel. We used it to measure the relative affinities of Pho4, AtERF2 and Btd full-length proteins to millions of different DNA binding sites, and detected both high and low-affinity interactions in equilibrium conditions, generating a comprehensive landscape of the relative TF affinities to all possible DNA 6-mers, and even DNA10-mers with increased sequencing depth. Low quantities of both the TFs and DNA oligomers were sufficient for obtaining high-quality results, significantly reducing experimental costs. SELMAP allows in-depth screening of hundreds of TFs, and provides a means for better understanding of the regulatory processes that govern gene expression.</description><subject>49/62</subject><subject>631/1647</subject><subject>631/61/191</subject><subject>Affinity</subject><subject>Binding sites</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA sequencing</subject><subject>Environmental changes</subject><subject>Gene expression</subject><subject>Humanities and Social Sciences</subject><subject>Microfluidics</subject><subject>multidisciplinary</subject><subject>Nucleotide sequence</subject><subject>Peptide mapping</subject><subject>Science</subject><subject>Transcription factors</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>BENPR</sourceid><recordid>eNplkVtrFDEYhoMottRe9A9IwJsqjM15JjeFUtYDrFhQoXchm8OaMptMk4zQf2_Wrctac5MP3of3O7wAnGH0HiM6XJTsJkopx8_AMUGMd4QS8vygPgKnpdyh9jiRDMuX4Ij0ggyU4WMQvy2WX65uYAdbsbiF2vsQQ32Ao462GD052OQpxDVMHtasYzE5TDWkCL02NWW4CtFu9RKqK3Au2zrE6tZZV2fhJpic_DgHG0x5BV54PRZ3-vifgB8fFt-vP3XLrx8_X18tO8PoUDtnPDJWMEOoFkPvV9g6bnSvheNIip5Zyy3Bfdub4IFgLjDRPdbMGayNYPQEXO58p3m1cda42EYf1ZTDRucHlXRQ_yox_FTr9EtxRBiRshmcPxrkdD-7UtUmFOPGdhaX5qJaV8SlkJw39M0T9C7NObb1GiUl6oX4M9HbHdWuUVpmfj8MRmobpNoH2djXh9Pvyb-xNeDdDihNimuXD1r-5_Ybl8GoAg</recordid><startdate>20160915</startdate><enddate>20160915</enddate><creator>Chen, Dana</creator><creator>Orenstein, Yaron</creator><creator>Golodnitsky, Rada</creator><creator>Pellach, Michal</creator><creator>Avrahami, Dorit</creator><creator>Wachtel, Chaim</creator><creator>Ovadia-Shochat, Avital</creator><creator>Shir-Shapira, Hila</creator><creator>Kedmi, Adi</creator><creator>Juven-Gershon, Tamar</creator><creator>Shamir, Ron</creator><creator>Gerber, Doron</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160915</creationdate><title>SELMAP - SELEX affinity landscape MAPping of transcription factor binding sites using integrated microfluidics</title><author>Chen, Dana ; 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These interactions are best portrayed as a landscape of TF binding affinities. Current methods to study sequence-specific binding preferences suffer from limited dynamic range, sequence bias, lack of specificity and limited throughput. We have developed a microfluidic-based device for SELEX Affinity Landscape MAPping (SELMAP) of TF binding, which allows high-throughput measurement of 16 proteins in parallel. We used it to measure the relative affinities of Pho4, AtERF2 and Btd full-length proteins to millions of different DNA binding sites, and detected both high and low-affinity interactions in equilibrium conditions, generating a comprehensive landscape of the relative TF affinities to all possible DNA 6-mers, and even DNA10-mers with increased sequencing depth. Low quantities of both the TFs and DNA oligomers were sufficient for obtaining high-quality results, significantly reducing experimental costs. SELMAP allows in-depth screening of hundreds of TFs, and provides a means for better understanding of the regulatory processes that govern gene expression.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>27628341</pmid><doi>10.1038/srep33351</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 49/62 631/1647 631/61/191 Affinity Binding sites Deoxyribonucleic acid DNA DNA sequencing Environmental changes Gene expression Humanities and Social Sciences Microfluidics multidisciplinary Nucleotide sequence Peptide mapping Science Transcription factors |
title | SELMAP - SELEX affinity landscape MAPping of transcription factor binding sites using integrated microfluidics |
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