Ptf1a Directly Controls Expression of Immunoglobulin Superfamily Molecules Nephrin and Neph3 in the Developing Central Nervous System
Ptf1a, a basic helix-loop-helix transcription factor, plays an indispensable role for cell fate specification of subsets of neurons in the developing central nervous system. However, downstream molecules induced by Ptf1a during neural development have not been well characterized. In the present stud...
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description | Ptf1a, a basic helix-loop-helix transcription factor, plays an indispensable role for cell fate specification of subsets of neurons in the developing central nervous system. However, downstream molecules induced by Ptf1a during neural development have not been well characterized. In the present study, we identified immunoglobulin superfamily molecules, Nephrin and Neph3, as direct downstream targets of Ptf1a. First, the expression domains of Nephrin and Neph3 closely resembled those of Ptf1a in the developing retina, hypothalamus, cerebellum, hindbrain, and spinal cord. Second, Ptf1a bound directly to a PTF-binding motif in the 5′-flanking region of Nephrin and Neph3 genes. Third, Ptf1a activated transcription driven by the 5′-flanking region of these genes. Finally, the expression of Nephrin and Neph3 was lost in Ptf1a-null mice, whereas ectopic expression of Nephrin and Neph3 was induced by forced expression of Ptf1a. We provided further evidence that Nephrin and Neph3 could interact homophilically and heterophilically, suggesting that Nephrin and Neph3 might regulate certain developmental aspects of Ptf1a-positive neurons as homo- or heterooligomers. |
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However, downstream molecules induced by Ptf1a during neural development have not been well characterized. In the present study, we identified immunoglobulin superfamily molecules, Nephrin and Neph3, as direct downstream targets of Ptf1a. First, the expression domains of Nephrin and Neph3 closely resembled those of Ptf1a in the developing retina, hypothalamus, cerebellum, hindbrain, and spinal cord. Second, Ptf1a bound directly to a PTF-binding motif in the 5′-flanking region of Nephrin and Neph3 genes. Third, Ptf1a activated transcription driven by the 5′-flanking region of these genes. Finally, the expression of Nephrin and Neph3 was lost in Ptf1a-null mice, whereas ectopic expression of Nephrin and Neph3 was induced by forced expression of Ptf1a. We provided further evidence that Nephrin and Neph3 could interact homophilically and heterophilically, suggesting that Nephrin and Neph3 might regulate certain developmental aspects of Ptf1a-positive neurons as homo- or heterooligomers.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M109.060657</identifier><identifier>PMID: 19887377</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>5' Flanking Region - genetics ; Animals ; Base Sequence ; Central Nervous System - cytology ; Central Nervous System - embryology ; Central Nervous System - metabolism ; Cerebral Cortex - cytology ; Cerebral Cortex - embryology ; Cerebral Cortex - metabolism ; Chlorocebus aethiops ; COS Cells ; Gene Expression Regulation ; Genes, Reporter ; Immunoglobulins - genetics ; Immunoglobulins - metabolism ; Luciferases - metabolism ; Membrane Proteins - genetics ; Membrane Proteins - metabolism ; Mice ; Molecular Basis of Cell and Developmental Biology ; Molecular Sequence Data ; Promoter Regions, Genetic - genetics ; Protein Binding ; Transcription Factors - deficiency ; Transcription Factors - genetics ; Transcription Factors - metabolism ; Transcription, Genetic</subject><ispartof>The Journal of biological chemistry, 2010-01, Vol.285 (1), p.373-380</ispartof><rights>2010 © 2010 ASBMB. 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However, downstream molecules induced by Ptf1a during neural development have not been well characterized. In the present study, we identified immunoglobulin superfamily molecules, Nephrin and Neph3, as direct downstream targets of Ptf1a. First, the expression domains of Nephrin and Neph3 closely resembled those of Ptf1a in the developing retina, hypothalamus, cerebellum, hindbrain, and spinal cord. Second, Ptf1a bound directly to a PTF-binding motif in the 5′-flanking region of Nephrin and Neph3 genes. Third, Ptf1a activated transcription driven by the 5′-flanking region of these genes. Finally, the expression of Nephrin and Neph3 was lost in Ptf1a-null mice, whereas ectopic expression of Nephrin and Neph3 was induced by forced expression of Ptf1a. We provided further evidence that Nephrin and Neph3 could interact homophilically and heterophilically, suggesting that Nephrin and Neph3 might regulate certain developmental aspects of Ptf1a-positive neurons as homo- or heterooligomers.</description><subject>5' Flanking Region - genetics</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Central Nervous System - cytology</subject><subject>Central Nervous System - embryology</subject><subject>Central Nervous System - metabolism</subject><subject>Cerebral Cortex - cytology</subject><subject>Cerebral Cortex - embryology</subject><subject>Cerebral Cortex - metabolism</subject><subject>Chlorocebus aethiops</subject><subject>COS Cells</subject><subject>Gene Expression Regulation</subject><subject>Genes, Reporter</subject><subject>Immunoglobulins - genetics</subject><subject>Immunoglobulins - metabolism</subject><subject>Luciferases - metabolism</subject><subject>Membrane Proteins - genetics</subject><subject>Membrane Proteins - metabolism</subject><subject>Mice</subject><subject>Molecular Basis of Cell and Developmental Biology</subject><subject>Molecular Sequence Data</subject><subject>Promoter Regions, Genetic - genetics</subject><subject>Protein Binding</subject><subject>Transcription Factors - deficiency</subject><subject>Transcription Factors - genetics</subject><subject>Transcription Factors - metabolism</subject><subject>Transcription, Genetic</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kktv1DAUhSMEokNhzQ7MBlaZ2nGc2BskNC1QqQWkKRI7y3FuEldOHOxkYH4A_xt3MuKxAG_8uJ-PzvVxkjwleE1wmZ_dVnp9TbBY4wIXrLyXrAjmNKWMfLmfrDDOSCoyxk-SRyHc4jhyQR4mJ0RwXtKyXCU_Pk0NUejceNCT3aONGybvbEAX30cPIRg3INegy76fB9daV83WDGg7j-Ab1Zt449pZ0LOFgD7A2PlYVUN9WFMUN1MH6Bx2YN1ohhZtIOorG-t-5-aAtvswQf84edAoG-DJcT5Nbt5e3Gzep1cf311u3lylmnExpXlWVFwohRvOCGUqI7XiWhChK5wzzKCk8UQJoCJvVAFFo7lWQkBWiRwrepq8XmTHueqh1osXOXrTK7-XThn5d2UwnWzdTmYc54SzKPDqKODd1xnCJHsTNFirBojdyJLmGcnj00by5X_JjNAMR8sRPFtA7V0IHppfdgiWdxnLmLG8y1guGccbz_7s4jd_DDUCLxagM233LSYrK-N0B33sg0ki6cHf84VplJOq9SbIz9sME4pJSUpaFJEQCwExkJ0BL4M2MGioD39F1s780-JP5hbNrQ</recordid><startdate>20100101</startdate><enddate>20100101</enddate><creator>Nishida, Kazuhiko</creator><creator>Hoshino, Mikio</creator><creator>Kawaguchi, Yoshiya</creator><creator>Murakami, Fujio</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><scope>FBQ</scope><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>7T5</scope><scope>7TK</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20100101</creationdate><title>Ptf1a Directly Controls Expression of Immunoglobulin Superfamily Molecules Nephrin and Neph3 in the Developing Central Nervous System</title><author>Nishida, Kazuhiko ; Hoshino, Mikio ; Kawaguchi, Yoshiya ; Murakami, Fujio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c589t-426b89aa0f85135a21da8c919cb04505e731daa9e394fa6e6fc8ca99e2b940a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>5' Flanking Region - genetics</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Central Nervous System - cytology</topic><topic>Central Nervous System - embryology</topic><topic>Central Nervous System - metabolism</topic><topic>Cerebral Cortex - cytology</topic><topic>Cerebral Cortex - embryology</topic><topic>Cerebral Cortex - metabolism</topic><topic>Chlorocebus aethiops</topic><topic>COS Cells</topic><topic>Gene Expression Regulation</topic><topic>Genes, Reporter</topic><topic>Immunoglobulins - genetics</topic><topic>Immunoglobulins - metabolism</topic><topic>Luciferases - metabolism</topic><topic>Membrane Proteins - genetics</topic><topic>Membrane Proteins - metabolism</topic><topic>Mice</topic><topic>Molecular Basis of Cell and Developmental Biology</topic><topic>Molecular Sequence Data</topic><topic>Promoter Regions, Genetic - genetics</topic><topic>Protein Binding</topic><topic>Transcription Factors - deficiency</topic><topic>Transcription Factors - genetics</topic><topic>Transcription Factors - metabolism</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nishida, Kazuhiko</creatorcontrib><creatorcontrib>Hoshino, Mikio</creatorcontrib><creatorcontrib>Kawaguchi, Yoshiya</creatorcontrib><creatorcontrib>Murakami, Fujio</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nishida, Kazuhiko</au><au>Hoshino, Mikio</au><au>Kawaguchi, Yoshiya</au><au>Murakami, Fujio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ptf1a Directly Controls Expression of Immunoglobulin Superfamily Molecules Nephrin and Neph3 in the Developing Central Nervous System</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2010-01-01</date><risdate>2010</risdate><volume>285</volume><issue>1</issue><spage>373</spage><epage>380</epage><pages>373-380</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Ptf1a, a basic helix-loop-helix transcription factor, plays an indispensable role for cell fate specification of subsets of neurons in the developing central nervous system. However, downstream molecules induced by Ptf1a during neural development have not been well characterized. In the present study, we identified immunoglobulin superfamily molecules, Nephrin and Neph3, as direct downstream targets of Ptf1a. First, the expression domains of Nephrin and Neph3 closely resembled those of Ptf1a in the developing retina, hypothalamus, cerebellum, hindbrain, and spinal cord. Second, Ptf1a bound directly to a PTF-binding motif in the 5′-flanking region of Nephrin and Neph3 genes. Third, Ptf1a activated transcription driven by the 5′-flanking region of these genes. Finally, the expression of Nephrin and Neph3 was lost in Ptf1a-null mice, whereas ectopic expression of Nephrin and Neph3 was induced by forced expression of Ptf1a. 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subjects | 5' Flanking Region - genetics Animals Base Sequence Central Nervous System - cytology Central Nervous System - embryology Central Nervous System - metabolism Cerebral Cortex - cytology Cerebral Cortex - embryology Cerebral Cortex - metabolism Chlorocebus aethiops COS Cells Gene Expression Regulation Genes, Reporter Immunoglobulins - genetics Immunoglobulins - metabolism Luciferases - metabolism Membrane Proteins - genetics Membrane Proteins - metabolism Mice Molecular Basis of Cell and Developmental Biology Molecular Sequence Data Promoter Regions, Genetic - genetics Protein Binding Transcription Factors - deficiency Transcription Factors - genetics Transcription Factors - metabolism Transcription, Genetic |
title | Ptf1a Directly Controls Expression of Immunoglobulin Superfamily Molecules Nephrin and Neph3 in the Developing Central Nervous System |
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