Triiodothyronine Has Diverse and Multiple Stimulating Effects on Expression of the Major Myelin Protein Genes

: If the importance of triiodothyronine (T3) on brain development including myelinogenesis has long been recognized, its mechanism of action at the gene level is still not fully elucidated. We studied the effect of T3 on the expression of myelin protein genes in aggregating brain cell cultures. T3 i...

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Veröffentlicht in:Journal of neurochemistry 1992-11, Vol.59 (5), p.1770-1777
Hauptverfasser: Tosic, Mirjana, Torch, Sakina, Comte, Véronique, Dolivo, Michel, Honegger, Paul, Matthieu, Jean‐Marie
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container_end_page 1777
container_issue 5
container_start_page 1770
container_title Journal of neurochemistry
container_volume 59
creator Tosic, Mirjana
Torch, Sakina
Comte, Véronique
Dolivo, Michel
Honegger, Paul
Matthieu, Jean‐Marie
description : If the importance of triiodothyronine (T3) on brain development including myelinogenesis has long been recognized, its mechanism of action at the gene level is still not fully elucidated. We studied the effect of T3 on the expression of myelin protein genes in aggregating brain cell cultures. T3 increases the concentrations of mRNA transcribed from the following four myelin protein genes: myelin basic protein (Mbp), myelin‐associated glycoprotein (Mag), proteolipid protein (Plp), and 2′,3′‐cyclic nucleotide 3′‐phosphodiesterase (Cnp). T3 is not only a triggering signal for oligodendrocyte differentiation, but it has continuous stimulatory effects on myelin gene expression. Transcription in isolated nuclei experiments shows that T3 increases Mag and Cnp transcription rates. After inhibiting transcription with actinomycin D, we measured the half‐lives of specific mRNAs. Our results show that T3 increases the stability of mRNA for myelin basic protein, and probably proteolipid protein. In vitro translation followed by myelin basic protein‐specific immunoprecipitation showed a direct stimulatory effect of T3 on myelin basic protein mRNA translation. Moreover, this stimulation was higher when the mRNA was already stabilized in culture, indicating that stabilization is achieved through mRNA structural modifications. These results demonstrate the diverse and multiple mechanisms of T3 stimulation of myelin protein genes.
doi_str_mv 10.1111/j.1471-4159.1992.tb11009.x
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We studied the effect of T3 on the expression of myelin protein genes in aggregating brain cell cultures. T3 increases the concentrations of mRNA transcribed from the following four myelin protein genes: myelin basic protein (Mbp), myelin‐associated glycoprotein (Mag), proteolipid protein (Plp), and 2′,3′‐cyclic nucleotide 3′‐phosphodiesterase (Cnp). T3 is not only a triggering signal for oligodendrocyte differentiation, but it has continuous stimulatory effects on myelin gene expression. Transcription in isolated nuclei experiments shows that T3 increases Mag and Cnp transcription rates. After inhibiting transcription with actinomycin D, we measured the half‐lives of specific mRNAs. Our results show that T3 increases the stability of mRNA for myelin basic protein, and probably proteolipid protein. In vitro translation followed by myelin basic protein‐specific immunoprecipitation showed a direct stimulatory effect of T3 on myelin basic protein mRNA translation. 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We studied the effect of T3 on the expression of myelin protein genes in aggregating brain cell cultures. T3 increases the concentrations of mRNA transcribed from the following four myelin protein genes: myelin basic protein (Mbp), myelin‐associated glycoprotein (Mag), proteolipid protein (Plp), and 2′,3′‐cyclic nucleotide 3′‐phosphodiesterase (Cnp). T3 is not only a triggering signal for oligodendrocyte differentiation, but it has continuous stimulatory effects on myelin gene expression. Transcription in isolated nuclei experiments shows that T3 increases Mag and Cnp transcription rates. After inhibiting transcription with actinomycin D, we measured the half‐lives of specific mRNAs. Our results show that T3 increases the stability of mRNA for myelin basic protein, and probably proteolipid protein. In vitro translation followed by myelin basic protein‐specific immunoprecipitation showed a direct stimulatory effect of T3 on myelin basic protein mRNA translation. 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Neuroglia</subject><subject>Myelin associated glycoprotein</subject><subject>Myelin basic protein</subject><subject>Myelin Basic Protein - biosynthesis</subject><subject>Myelin Basic Protein - drug effects</subject><subject>Myelin Basic Protein - genetics</subject><subject>Protein Biosynthesis - drug effects</subject><subject>Proteolipid protein</subject><subject>Rats</subject><subject>RNA, Messenger - drug effects</subject><subject>Telencephalon - drug effects</subject><subject>Telencephalon - metabolism</subject><subject>Transcription, Genetic - drug effects</subject><subject>Triiodothyronine</subject><subject>Triiodothyronine - pharmacology</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkV2L1DAUhoMo67j6E4QgIt60njRparxZZBx3lR0VXK9Dmp64GTrNmLQ68-9NmWG9U8zNCbzP-YCHkGcMSpbfq03JRMMKwWpVMqWqcmwZA1Dl_h5Z3EX3yQKgqgoOonpIHqW0AWBSSHZGzhh_zUUlF2R7E70PXRhvDzEMfkB6ZRJ9539iTEjN0NH11I9-1yP9Ovrt1JvRD9_pyjm0Y6JhoKv9LmJKPn-Do-Mt0rXZhEjXB-z9QL_EMGKulzhgekweONMnfHKq5-Tb-9XN8qq4_nz5Yfn2urBCcigsbztseS0Fs1WFqrZStkYK17YA0rVQM7DWSGwNB6kUdFwhcnCmEQ6amp-TF8e5uxh-TJhGvfXJYt-bAcOUdMOrPLyW_wSZrEGC4hl8-XcwQ6JWwFhG3xxRG0NKEZ3eRb818ZAhPfvTGz1L0rMkPfvTJ396n5ufnvZM7Ra7P61HYTl_fspNsqZ30QzWpztM8LoBPp97ccR--R4P_3GA_vhpyZo84zcZjLf6</recordid><startdate>199211</startdate><enddate>199211</enddate><creator>Tosic, Mirjana</creator><creator>Torch, Sakina</creator><creator>Comte, Véronique</creator><creator>Dolivo, Michel</creator><creator>Honegger, Paul</creator><creator>Matthieu, Jean‐Marie</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>IQODW</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>7TK</scope><scope>7X8</scope></search><sort><creationdate>199211</creationdate><title>Triiodothyronine Has Diverse and Multiple Stimulating Effects on Expression of the Major Myelin Protein Genes</title><author>Tosic, Mirjana ; Torch, Sakina ; Comte, Véronique ; Dolivo, Michel ; Honegger, Paul ; Matthieu, Jean‐Marie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4630-c3bdeb35641c22e95c66ba64fbb006fb0510cca6eba306990d39ee30fa74f0753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>2′,3′‐Cyclic nucleotide 3′‐phosphodiesterase</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cells, Cultured</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Isolated neuron and nerve. Neuroglia</topic><topic>Myelin associated glycoprotein</topic><topic>Myelin basic protein</topic><topic>Myelin Basic Protein - biosynthesis</topic><topic>Myelin Basic Protein - drug effects</topic><topic>Myelin Basic Protein - genetics</topic><topic>Protein Biosynthesis - drug effects</topic><topic>Proteolipid protein</topic><topic>Rats</topic><topic>RNA, Messenger - drug effects</topic><topic>Telencephalon - drug effects</topic><topic>Telencephalon - metabolism</topic><topic>Transcription, Genetic - drug effects</topic><topic>Triiodothyronine</topic><topic>Triiodothyronine - pharmacology</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tosic, Mirjana</creatorcontrib><creatorcontrib>Torch, Sakina</creatorcontrib><creatorcontrib>Comte, Véronique</creatorcontrib><creatorcontrib>Dolivo, Michel</creatorcontrib><creatorcontrib>Honegger, Paul</creatorcontrib><creatorcontrib>Matthieu, Jean‐Marie</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tosic, Mirjana</au><au>Torch, Sakina</au><au>Comte, Véronique</au><au>Dolivo, Michel</au><au>Honegger, Paul</au><au>Matthieu, Jean‐Marie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Triiodothyronine Has Diverse and Multiple Stimulating Effects on Expression of the Major Myelin Protein Genes</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>1992-11</date><risdate>1992</risdate><volume>59</volume><issue>5</issue><spage>1770</spage><epage>1777</epage><pages>1770-1777</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>: If the importance of triiodothyronine (T3) on brain development including myelinogenesis has long been recognized, its mechanism of action at the gene level is still not fully elucidated. We studied the effect of T3 on the expression of myelin protein genes in aggregating brain cell cultures. T3 increases the concentrations of mRNA transcribed from the following four myelin protein genes: myelin basic protein (Mbp), myelin‐associated glycoprotein (Mag), proteolipid protein (Plp), and 2′,3′‐cyclic nucleotide 3′‐phosphodiesterase (Cnp). T3 is not only a triggering signal for oligodendrocyte differentiation, but it has continuous stimulatory effects on myelin gene expression. Transcription in isolated nuclei experiments shows that T3 increases Mag and Cnp transcription rates. After inhibiting transcription with actinomycin D, we measured the half‐lives of specific mRNAs. Our results show that T3 increases the stability of mRNA for myelin basic protein, and probably proteolipid protein. In vitro translation followed by myelin basic protein‐specific immunoprecipitation showed a direct stimulatory effect of T3 on myelin basic protein mRNA translation. Moreover, this stimulation was higher when the mRNA was already stabilized in culture, indicating that stabilization is achieved through mRNA structural modifications. These results demonstrate the diverse and multiple mechanisms of T3 stimulation of myelin protein genes.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>1383426</pmid><doi>10.1111/j.1471-4159.1992.tb11009.x</doi><tpages>8</tpages></addata></record>
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subjects 2′,3′‐Cyclic nucleotide 3′‐phosphodiesterase
Animals
Biological and medical sciences
Cells, Cultured
Fundamental and applied biological sciences. Psychology
Gene Expression Regulation - drug effects
Isolated neuron and nerve. Neuroglia
Myelin associated glycoprotein
Myelin basic protein
Myelin Basic Protein - biosynthesis
Myelin Basic Protein - drug effects
Myelin Basic Protein - genetics
Protein Biosynthesis - drug effects
Proteolipid protein
Rats
RNA, Messenger - drug effects
Telencephalon - drug effects
Telencephalon - metabolism
Transcription, Genetic - drug effects
Triiodothyronine
Triiodothyronine - pharmacology
Vertebrates: nervous system and sense organs
title Triiodothyronine Has Diverse and Multiple Stimulating Effects on Expression of the Major Myelin Protein Genes
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