Definition of the transcription factor TdIF1 consensus‐binding sequence through genomewide mapping of its binding sites
TdIF1 was originally identified as a protein that directly binds to terminal deoxynucleotidyltransferase, TdT. Through in vitro selection assays (SELEX), we recently showed that TdIF1 recognizes both AT‐tract and a specific DNA sequence motif, 5′‐TGCATG‐3′, and can up‐regulate the expression of RAB2...
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Veröffentlicht in: | Genes to cells : devoted to molecular & cellular mechanisms 2015-03, Vol.20 (3), p.242-254 |
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creator | Koiwai, Kotaro Kubota, Takashi Watanabe, Nobuhisa Hori, Katsutoshi Koiwai, Osamu Masai, Hisao |
description | TdIF1 was originally identified as a protein that directly binds to terminal deoxynucleotidyltransferase, TdT. Through in vitro selection assays (SELEX), we recently showed that TdIF1 recognizes both AT‐tract and a specific DNA sequence motif, 5′‐TGCATG‐3′, and can up‐regulate the expression of RAB20 through the latter motif. However, whether TdIF1 binds to these sequences in the cells has not been clear and its other target genes remain to be identified. Here, we determined in vivo TdIF1‐binding sequences (TdIF1‐invivoBMs) on the human chromosomes through ChIP‐seq analyses. The result showed a 160‐base pair cassette containing ‘AT‐tract~palindrome (inverted repeat)~AT‐tract’ as a likely target sequence of TdIF1. Interestingly, the core sequence of the palindrome in the TdIF1‐invivoBMs shares significant similarity to the above 5′‐TGCATG‐3′ motif determined by SELEX in vitro. Furthermore, spacer sequences between AT‐tract and the palindrome contain many potential transcription factor binding sites. In luciferase assays, TdIF1 can up‐regulate transcription activity of the promoters containing the TdIF1‐invivoBM, and this effect is mainly through the palindrome. Clusters of this motif were found in the potential target genes. Gene ontology analysis and RT‐qPCR showed the enrichment of some candidate targets of TdIF1 among the genes involved in the regulation of ossification. Potential modes of transcription activation by TdIF1 are discussed. |
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Through in vitro selection assays (SELEX), we recently showed that TdIF1 recognizes both AT‐tract and a specific DNA sequence motif, 5′‐TGCATG‐3′, and can up‐regulate the expression of RAB20 through the latter motif. However, whether TdIF1 binds to these sequences in the cells has not been clear and its other target genes remain to be identified. Here, we determined in vivo TdIF1‐binding sequences (TdIF1‐invivoBMs) on the human chromosomes through ChIP‐seq analyses. The result showed a 160‐base pair cassette containing ‘AT‐tract~palindrome (inverted repeat)~AT‐tract’ as a likely target sequence of TdIF1. Interestingly, the core sequence of the palindrome in the TdIF1‐invivoBMs shares significant similarity to the above 5′‐TGCATG‐3′ motif determined by SELEX in vitro. Furthermore, spacer sequences between AT‐tract and the palindrome contain many potential transcription factor binding sites. In luciferase assays, TdIF1 can up‐regulate transcription activity of the promoters containing the TdIF1‐invivoBM, and this effect is mainly through the palindrome. Clusters of this motif were found in the potential target genes. Gene ontology analysis and RT‐qPCR showed the enrichment of some candidate targets of TdIF1 among the genes involved in the regulation of ossification. Potential modes of transcription activation by TdIF1 are discussed.</description><identifier>ISSN: 1356-9597</identifier><identifier>EISSN: 1365-2443</identifier><identifier>DOI: 10.1111/gtc.12216</identifier><identifier>PMID: 25619743</identifier><identifier>CODEN: GECEFL</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Binding Sites ; Carrier Proteins - chemistry ; Carrier Proteins - metabolism ; Cell Line ; Chromatin Immunoprecipitation ; Chromosome Mapping - methods ; Genes ; Humans ; Nuclear Proteins - chemistry ; Nuclear Proteins - metabolism ; Osteogenesis ; Response Elements - genetics ; Transcription factors ; Transcription Factors - chemistry ; Transcription Factors - metabolism</subject><ispartof>Genes to cells : devoted to molecular & cellular mechanisms, 2015-03, Vol.20 (3), p.242-254</ispartof><rights>2015 The Authors Genes to Cells © 2015 by the Molecular Biology Society of Japan and Wiley Publishing Asia Pty Ltd</rights><rights>2015 The Authors Genes to Cells © 2015 by the Molecular Biology Society of Japan and Wiley Publishing Asia Pty Ltd.</rights><rights>Copyright © 2015 by the Molecular Biology Society of Japan and Wiley Publishing Asia Pty Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fgtc.12216$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fgtc.12216$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25619743$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Koiwai, Kotaro</creatorcontrib><creatorcontrib>Kubota, Takashi</creatorcontrib><creatorcontrib>Watanabe, Nobuhisa</creatorcontrib><creatorcontrib>Hori, Katsutoshi</creatorcontrib><creatorcontrib>Koiwai, Osamu</creatorcontrib><creatorcontrib>Masai, Hisao</creatorcontrib><title>Definition of the transcription factor TdIF1 consensus‐binding sequence through genomewide mapping of its binding sites</title><title>Genes to cells : devoted to molecular & cellular mechanisms</title><addtitle>Genes Cells</addtitle><description>TdIF1 was originally identified as a protein that directly binds to terminal deoxynucleotidyltransferase, TdT. Through in vitro selection assays (SELEX), we recently showed that TdIF1 recognizes both AT‐tract and a specific DNA sequence motif, 5′‐TGCATG‐3′, and can up‐regulate the expression of RAB20 through the latter motif. However, whether TdIF1 binds to these sequences in the cells has not been clear and its other target genes remain to be identified. Here, we determined in vivo TdIF1‐binding sequences (TdIF1‐invivoBMs) on the human chromosomes through ChIP‐seq analyses. The result showed a 160‐base pair cassette containing ‘AT‐tract~palindrome (inverted repeat)~AT‐tract’ as a likely target sequence of TdIF1. Interestingly, the core sequence of the palindrome in the TdIF1‐invivoBMs shares significant similarity to the above 5′‐TGCATG‐3′ motif determined by SELEX in vitro. Furthermore, spacer sequences between AT‐tract and the palindrome contain many potential transcription factor binding sites. In luciferase assays, TdIF1 can up‐regulate transcription activity of the promoters containing the TdIF1‐invivoBM, and this effect is mainly through the palindrome. Clusters of this motif were found in the potential target genes. Gene ontology analysis and RT‐qPCR showed the enrichment of some candidate targets of TdIF1 among the genes involved in the regulation of ossification. Potential modes of transcription activation by TdIF1 are discussed.</description><subject>Binding Sites</subject><subject>Carrier Proteins - chemistry</subject><subject>Carrier Proteins - metabolism</subject><subject>Cell Line</subject><subject>Chromatin Immunoprecipitation</subject><subject>Chromosome Mapping - methods</subject><subject>Genes</subject><subject>Humans</subject><subject>Nuclear Proteins - chemistry</subject><subject>Nuclear Proteins - metabolism</subject><subject>Osteogenesis</subject><subject>Response Elements - genetics</subject><subject>Transcription factors</subject><subject>Transcription Factors - chemistry</subject><subject>Transcription Factors - metabolism</subject><issn>1356-9597</issn><issn>1365-2443</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkb1OwzAQxy0EoqUw8ALIEgtLWn-nGVGhpVIlljJHru20rho7xImqbjwCz8iT4H7AwISXO9397m-f_wDcYtTH8QyWjepjQrA4A11MBU8IY_R8n3ORZDxLO-AqhDVCmBLEL0GHcIGzlNEu2D2ZwjrbWO-gL2CzMrCppQuqttWhWEjV-BrO9XSMofIuGBfa8PXxubBOW7eEwby3xqk4t6p9u1zBpXG-NFurDSxlVe2ZqGybAH9HbGPCNbgo5CaYm1Psgbfx83z0ksxeJ9PR4yxZsyEViRRKY6KxFpnUKdKKxRUKRhaMZAUbcoUzwYyURmguYg0VOpMYUYUpIgUVtAcejrpV7eNLQ5OXNiiz2UhnfBtyLNIomXI-_Acab8CUCR7R-z_o2re1i4tEimdIUJGiSN2dqHZRGp1XtS1lvct__j8CgyOwtRuz--1jlO-NzaOx-cHYfDIfHRL6DfSDli4</recordid><startdate>201503</startdate><enddate>201503</enddate><creator>Koiwai, Kotaro</creator><creator>Kubota, Takashi</creator><creator>Watanabe, Nobuhisa</creator><creator>Hori, Katsutoshi</creator><creator>Koiwai, Osamu</creator><creator>Masai, Hisao</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201503</creationdate><title>Definition of the transcription factor TdIF1 consensus‐binding sequence through genomewide mapping of its binding sites</title><author>Koiwai, Kotaro ; 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Through in vitro selection assays (SELEX), we recently showed that TdIF1 recognizes both AT‐tract and a specific DNA sequence motif, 5′‐TGCATG‐3′, and can up‐regulate the expression of RAB20 through the latter motif. However, whether TdIF1 binds to these sequences in the cells has not been clear and its other target genes remain to be identified. Here, we determined in vivo TdIF1‐binding sequences (TdIF1‐invivoBMs) on the human chromosomes through ChIP‐seq analyses. The result showed a 160‐base pair cassette containing ‘AT‐tract~palindrome (inverted repeat)~AT‐tract’ as a likely target sequence of TdIF1. Interestingly, the core sequence of the palindrome in the TdIF1‐invivoBMs shares significant similarity to the above 5′‐TGCATG‐3′ motif determined by SELEX in vitro. Furthermore, spacer sequences between AT‐tract and the palindrome contain many potential transcription factor binding sites. 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subjects | Binding Sites Carrier Proteins - chemistry Carrier Proteins - metabolism Cell Line Chromatin Immunoprecipitation Chromosome Mapping - methods Genes Humans Nuclear Proteins - chemistry Nuclear Proteins - metabolism Osteogenesis Response Elements - genetics Transcription factors Transcription Factors - chemistry Transcription Factors - metabolism |
title | Definition of the transcription factor TdIF1 consensus‐binding sequence through genomewide mapping of its binding sites |
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