Transcriptional Regulation of Tal2 Gene by All-trans Retinoic Acid (atRA) in P19 Cells
TAL2 is a transcription factor required in the normal development of mouse brain. In a previous study, we demonstrated that the expression of Tal2 gene is induced by the complex of all-trans retinoic acid (atRA) and retinoic acid receptor α (RARα) in mouse embryonal carcinoma P19 cells. atRA is also...
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description | TAL2 is a transcription factor required in the normal development of mouse brain. In a previous study, we demonstrated that the expression of Tal2 gene is induced by the complex of all-trans retinoic acid (atRA) and retinoic acid receptor α (RARα) in mouse embryonal carcinoma P19 cells. atRA is also known to be important in inducing P19 cells to differentiate into the neural lineage. Therefore, we believe that the function of TAL2 in neural differentiation may be clarified by utilizing P19 cells. As the atRA-RARα complex induced the expression of Tal2, we focused on the regulatory region that is involved in its transcription. The atRA-RARα complex occupies a characteristic retinoic acid response element (RARE) located in the promoter of target genes. Therefore, we searched for RARE on the mouse Tal2 and found that a RARE-like element was located in the intron. We also found that a TATA-box-like element was located in the 5′-region of Tal2. Involvement between transcriptional activity and the TATA-box-like element was confirmed in the luciferase assay, and TATA-box binding protein was bound to this element upstream of Tal2 in P19 cells. atRA signaling activated the transcription through the RARE-like element, and RARα was bound to this element on Tal2 in P19 cells. In addition, the interaction between these elements on Tal2 was shown in the chromatin immunoprecipitation assay. These results suggest that the transcription of Tal2 is coordinately mediated by two distal regulatory elements. |
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In a previous study, we demonstrated that the expression of Tal2 gene is induced by the complex of all-trans retinoic acid (atRA) and retinoic acid receptor α (RARα) in mouse embryonal carcinoma P19 cells. atRA is also known to be important in inducing P19 cells to differentiate into the neural lineage. Therefore, we believe that the function of TAL2 in neural differentiation may be clarified by utilizing P19 cells. As the atRA-RARα complex induced the expression of Tal2, we focused on the regulatory region that is involved in its transcription. The atRA-RARα complex occupies a characteristic retinoic acid response element (RARE) located in the promoter of target genes. Therefore, we searched for RARE on the mouse Tal2 and found that a RARE-like element was located in the intron. We also found that a TATA-box-like element was located in the 5′-region of Tal2. Involvement between transcriptional activity and the TATA-box-like element was confirmed in the luciferase assay, and TATA-box binding protein was bound to this element upstream of Tal2 in P19 cells. atRA signaling activated the transcription through the RARE-like element, and RARα was bound to this element on Tal2 in P19 cells. In addition, the interaction between these elements on Tal2 was shown in the chromatin immunoprecipitation assay. These results suggest that the transcription of Tal2 is coordinately mediated by two distal regulatory elements.</description><identifier>ISSN: 0918-6158</identifier><identifier>EISSN: 1347-5215</identifier><identifier>DOI: 10.1248/bpb.b14-00617</identifier><identifier>PMID: 25482166</identifier><language>eng</language><publisher>Japan: The Pharmaceutical Society of Japan</publisher><subject>Animals ; Basic Helix-Loop-Helix Transcription Factors - genetics ; Basic Helix-Loop-Helix Transcription Factors - metabolism ; Cell Line, Tumor ; DNA, Complementary - genetics ; Mice ; Neoplasm Proteins - genetics ; Neoplasm Proteins - metabolism ; Regulatory Elements, Transcriptional ; retinoic acid receptor α (RARα) ; retinoic acid response element (RARE) ; Tal2 gene ; TATA-box ; TATA-box binding protein (TBP) ; Transcription, Genetic ; Tretinoin - pharmacology</subject><ispartof>Biological and Pharmaceutical Bulletin, 2015/02/01, Vol.38(2), pp.248-256</ispartof><rights>2015 The Pharmaceutical Society of Japan</rights><rights>Copyright Japan Science and Technology Agency 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c735t-38af2960ff79c4ce72696c5e66d581c7cc9b7a22ab4e33c823cda50cecc898833</citedby><cites>FETCH-LOGICAL-c735t-38af2960ff79c4ce72696c5e66d581c7cc9b7a22ab4e33c823cda50cecc898833</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25482166$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kobayashi, Takanobu</creatorcontrib><creatorcontrib>Suzuki, Masayo</creatorcontrib><creatorcontrib>Morikawa, Masayuki</creatorcontrib><creatorcontrib>Kino, Katsuhito</creatorcontrib><creatorcontrib>Tanuma, Sei-ichi</creatorcontrib><creatorcontrib>Miyazawa, Hiroshi</creatorcontrib><creatorcontrib>aKagawa School of Pharmaceutical Sciences</creatorcontrib><creatorcontrib>Faculty of Pharmaceutical Sciences</creatorcontrib><creatorcontrib>Tokyo University of Science</creatorcontrib><creatorcontrib>Tokushima Bunri University</creatorcontrib><creatorcontrib>bDepartment of Biochemistry</creatorcontrib><title>Transcriptional Regulation of Tal2 Gene by All-trans Retinoic Acid (atRA) in P19 Cells</title><title>Biological & pharmaceutical bulletin</title><addtitle>Biol Pharm Bull</addtitle><description>TAL2 is a transcription factor required in the normal development of mouse brain. In a previous study, we demonstrated that the expression of Tal2 gene is induced by the complex of all-trans retinoic acid (atRA) and retinoic acid receptor α (RARα) in mouse embryonal carcinoma P19 cells. atRA is also known to be important in inducing P19 cells to differentiate into the neural lineage. Therefore, we believe that the function of TAL2 in neural differentiation may be clarified by utilizing P19 cells. As the atRA-RARα complex induced the expression of Tal2, we focused on the regulatory region that is involved in its transcription. The atRA-RARα complex occupies a characteristic retinoic acid response element (RARE) located in the promoter of target genes. Therefore, we searched for RARE on the mouse Tal2 and found that a RARE-like element was located in the intron. We also found that a TATA-box-like element was located in the 5′-region of Tal2. Involvement between transcriptional activity and the TATA-box-like element was confirmed in the luciferase assay, and TATA-box binding protein was bound to this element upstream of Tal2 in P19 cells. atRA signaling activated the transcription through the RARE-like element, and RARα was bound to this element on Tal2 in P19 cells. In addition, the interaction between these elements on Tal2 was shown in the chromatin immunoprecipitation assay. These results suggest that the transcription of Tal2 is coordinately mediated by two distal regulatory elements.</description><subject>Animals</subject><subject>Basic Helix-Loop-Helix Transcription Factors - genetics</subject><subject>Basic Helix-Loop-Helix Transcription Factors - metabolism</subject><subject>Cell Line, Tumor</subject><subject>DNA, Complementary - genetics</subject><subject>Mice</subject><subject>Neoplasm Proteins - genetics</subject><subject>Neoplasm Proteins - metabolism</subject><subject>Regulatory Elements, Transcriptional</subject><subject>retinoic acid receptor α (RARα)</subject><subject>retinoic acid response element (RARE)</subject><subject>Tal2 gene</subject><subject>TATA-box</subject><subject>TATA-box binding protein (TBP)</subject><subject>Transcription, Genetic</subject><subject>Tretinoin - pharmacology</subject><issn>0918-6158</issn><issn>1347-5215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUtrGzEUhUVpady0y26LoJt0MYkeo9fSmNYtBFKC063QXGtSGXnkSjOL_Pto4tSFrrKQxOV-nHPQQegjJZeUtfqqO3SXHW0bQiRVr9CC8lY1glHxGi2IobqRVOgz9K6UHSFEEcbfojMmWs2olAv0a5PdUCCHwxjS4CK-9fdTdPOAU483LjK89oPH3QNextiMM16hMQwpAF5C2OILN94uv-Aw4J_U4JWPsbxHb3oXi__w_J6ju29fN6vvzfXN-sdqed2A4mJsuHY9M5L0vTLQgldMGgnCS7kVmoICMJ1yjLmu9ZyDZhy2ThDwANpozfk5ujjqHnL6M_ky2n0oUBO4waepWKqpkIZR_gJUSmoMb6Wq6Of_0F2acv2dSinBhTBKzVRzpCCnUrLv7SGHvcsPlhI7d2NrN7Z2Y5-6qfynZ9Wp2_vtif5bRgXWR6BuA7iYhhgG_88biupCiskyQkUV5ZowS2g9sxlhQrKWEGF0VVodlXZldPf-ZOXyGCD6p2BcWzZfp4CnLfx22fqBPwIvlbVL</recordid><startdate>20150201</startdate><enddate>20150201</enddate><creator>Kobayashi, Takanobu</creator><creator>Suzuki, Masayo</creator><creator>Morikawa, Masayuki</creator><creator>Kino, Katsuhito</creator><creator>Tanuma, Sei-ichi</creator><creator>Miyazawa, Hiroshi</creator><general>The Pharmaceutical Society of Japan</general><general>Pharmaceutical Society of Japan</general><general>Japan Science and Technology Agency</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><scope>RC3</scope></search><sort><creationdate>20150201</creationdate><title>Transcriptional Regulation of Tal2 Gene by All-trans Retinoic Acid (atRA) in P19 Cells</title><author>Kobayashi, Takanobu ; Suzuki, Masayo ; Morikawa, Masayuki ; Kino, Katsuhito ; Tanuma, Sei-ichi ; Miyazawa, Hiroshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c735t-38af2960ff79c4ce72696c5e66d581c7cc9b7a22ab4e33c823cda50cecc898833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Basic Helix-Loop-Helix Transcription Factors - genetics</topic><topic>Basic Helix-Loop-Helix Transcription Factors - metabolism</topic><topic>Cell Line, Tumor</topic><topic>DNA, Complementary - genetics</topic><topic>Mice</topic><topic>Neoplasm Proteins - genetics</topic><topic>Neoplasm Proteins - metabolism</topic><topic>Regulatory Elements, Transcriptional</topic><topic>retinoic acid receptor α (RARα)</topic><topic>retinoic acid response element (RARE)</topic><topic>Tal2 gene</topic><topic>TATA-box</topic><topic>TATA-box binding protein (TBP)</topic><topic>Transcription, Genetic</topic><topic>Tretinoin - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kobayashi, Takanobu</creatorcontrib><creatorcontrib>Suzuki, Masayo</creatorcontrib><creatorcontrib>Morikawa, Masayuki</creatorcontrib><creatorcontrib>Kino, Katsuhito</creatorcontrib><creatorcontrib>Tanuma, Sei-ichi</creatorcontrib><creatorcontrib>Miyazawa, Hiroshi</creatorcontrib><creatorcontrib>aKagawa School of Pharmaceutical Sciences</creatorcontrib><creatorcontrib>Faculty of Pharmaceutical Sciences</creatorcontrib><creatorcontrib>Tokyo University of Science</creatorcontrib><creatorcontrib>Tokushima Bunri University</creatorcontrib><creatorcontrib>bDepartment of Biochemistry</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Genetics Abstracts</collection><jtitle>Biological & pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kobayashi, Takanobu</au><au>Suzuki, Masayo</au><au>Morikawa, Masayuki</au><au>Kino, Katsuhito</au><au>Tanuma, Sei-ichi</au><au>Miyazawa, Hiroshi</au><aucorp>aKagawa School of Pharmaceutical Sciences</aucorp><aucorp>Faculty of Pharmaceutical Sciences</aucorp><aucorp>Tokyo University of Science</aucorp><aucorp>Tokushima Bunri University</aucorp><aucorp>bDepartment of Biochemistry</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transcriptional Regulation of Tal2 Gene by All-trans Retinoic Acid (atRA) in P19 Cells</atitle><jtitle>Biological & pharmaceutical bulletin</jtitle><addtitle>Biol Pharm Bull</addtitle><date>2015-02-01</date><risdate>2015</risdate><volume>38</volume><issue>2</issue><spage>248</spage><epage>256</epage><pages>248-256</pages><issn>0918-6158</issn><eissn>1347-5215</eissn><abstract>TAL2 is a transcription factor required in the normal development of mouse brain. In a previous study, we demonstrated that the expression of Tal2 gene is induced by the complex of all-trans retinoic acid (atRA) and retinoic acid receptor α (RARα) in mouse embryonal carcinoma P19 cells. atRA is also known to be important in inducing P19 cells to differentiate into the neural lineage. Therefore, we believe that the function of TAL2 in neural differentiation may be clarified by utilizing P19 cells. As the atRA-RARα complex induced the expression of Tal2, we focused on the regulatory region that is involved in its transcription. The atRA-RARα complex occupies a characteristic retinoic acid response element (RARE) located in the promoter of target genes. Therefore, we searched for RARE on the mouse Tal2 and found that a RARE-like element was located in the intron. We also found that a TATA-box-like element was located in the 5′-region of Tal2. Involvement between transcriptional activity and the TATA-box-like element was confirmed in the luciferase assay, and TATA-box binding protein was bound to this element upstream of Tal2 in P19 cells. atRA signaling activated the transcription through the RARE-like element, and RARα was bound to this element on Tal2 in P19 cells. In addition, the interaction between these elements on Tal2 was shown in the chromatin immunoprecipitation assay. These results suggest that the transcription of Tal2 is coordinately mediated by two distal regulatory elements.</abstract><cop>Japan</cop><pub>The Pharmaceutical Society of Japan</pub><pmid>25482166</pmid><doi>10.1248/bpb.b14-00617</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Basic Helix-Loop-Helix Transcription Factors - genetics Basic Helix-Loop-Helix Transcription Factors - metabolism Cell Line, Tumor DNA, Complementary - genetics Mice Neoplasm Proteins - genetics Neoplasm Proteins - metabolism Regulatory Elements, Transcriptional retinoic acid receptor α (RARα) retinoic acid response element (RARE) Tal2 gene TATA-box TATA-box binding protein (TBP) Transcription, Genetic Tretinoin - pharmacology |
title | Transcriptional Regulation of Tal2 Gene by All-trans Retinoic Acid (atRA) in P19 Cells |
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