More than just Stem Cells: Functional Roles of the Transcription Factor Sox2 in Differentiated Glia and Neurons
The Sox2 transcription factor, encoded by a gene conserved in animal evolution, has become widely known because of its functional relevance for stem cells. In the developing nervous system, Sox2 is active in neural stem cells, and important for their self-renewal; differentiation to neurons and glia...
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description | The Sox2 transcription factor, encoded by a gene conserved in animal evolution, has become widely known because of its functional relevance for stem cells. In the developing nervous system, Sox2 is active in neural stem cells, and important for their self-renewal; differentiation to neurons and glia normally involves Sox2 downregulation. Recent evidence, however, identified specific types of fully differentiated neurons and glia that retain high Sox2 expression, and critically require Sox2 function, as revealed by functional studies in mouse and in other animals. Sox2 was found to control fundamental aspects of the biology of these cells, such as the development of correct neuronal connectivity. Sox2 downstream target genes identified within these cell types provide molecular mechanisms for cell-type-specific Sox2 neuronal and glial functions. SOX2 mutations in humans lead to a spectrum of nervous system defects, involving vision, movement control, and cognition; the identification of neurons and glia requiring Sox2 function, and the investigation of Sox2 roles and molecular targets within them, represents a novel perspective for the understanding of the pathogenesis of these defects. |
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In the developing nervous system, Sox2 is active in neural stem cells, and important for their self-renewal; differentiation to neurons and glia normally involves Sox2 downregulation. Recent evidence, however, identified specific types of fully differentiated neurons and glia that retain high Sox2 expression, and critically require Sox2 function, as revealed by functional studies in mouse and in other animals. Sox2 was found to control fundamental aspects of the biology of these cells, such as the development of correct neuronal connectivity. Sox2 downstream target genes identified within these cell types provide molecular mechanisms for cell-type-specific Sox2 neuronal and glial functions. SOX2 mutations in humans lead to a spectrum of nervous system defects, involving vision, movement control, and cognition; the identification of neurons and glia requiring Sox2 function, and the investigation of Sox2 roles and molecular targets within them, represents a novel perspective for the understanding of the pathogenesis of these defects.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms20184540</identifier><identifier>PMID: 31540269</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Abnormalities ; Animals ; Astrocytes ; Ataxia ; Basal ganglia ; Binding sites ; Cell adhesion & migration ; Cell Differentiation ; Cell Self Renewal ; Clonal deletion ; Defects ; Down-Regulation ; Embryogenesis ; Enhancers ; Epigenetics ; Forebrain ; Gene expression ; Genes ; Glial cells ; Hippocampus ; Humans ; Intellectual disabilities ; Mice ; Morphology ; Motor task performance ; Mutants ; Mutation ; Nervous system ; Neural Stem Cells - cytology ; Neural Stem Cells - metabolism ; Neurodevelopmental disorders ; Neurogenesis ; Neuroglia - cytology ; Neuroglia - metabolism ; Neuronal-glial interactions ; Phenotypes ; Primordia ; Radial glial cells ; Review ; Roles ; Seizures ; Signal Transduction ; SOXB1 Transcription Factors - genetics ; SOXB1 Transcription Factors - metabolism ; Stem cells ; Substantia alba ; Thyroid transcription factor 1 ; Transcription factors</subject><ispartof>International journal of molecular sciences, 2019-09, Vol.20 (18), p.4540</ispartof><rights>2019. This work is licensed under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 by the authors. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-2d230d3612b27e0fdaa344b3542efdb95365685ce004ac664791f132e988de153</citedby><cites>FETCH-LOGICAL-c478t-2d230d3612b27e0fdaa344b3542efdb95365685ce004ac664791f132e988de153</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/PMC6769708/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769708/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31540269$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mercurio, Sara</creatorcontrib><creatorcontrib>Serra, Linda</creatorcontrib><creatorcontrib>Nicolis, Silvia K</creatorcontrib><title>More than just Stem Cells: Functional Roles of the Transcription Factor Sox2 in Differentiated Glia and Neurons</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>The Sox2 transcription factor, encoded by a gene conserved in animal evolution, has become widely known because of its functional relevance for stem cells. In the developing nervous system, Sox2 is active in neural stem cells, and important for their self-renewal; differentiation to neurons and glia normally involves Sox2 downregulation. Recent evidence, however, identified specific types of fully differentiated neurons and glia that retain high Sox2 expression, and critically require Sox2 function, as revealed by functional studies in mouse and in other animals. Sox2 was found to control fundamental aspects of the biology of these cells, such as the development of correct neuronal connectivity. Sox2 downstream target genes identified within these cell types provide molecular mechanisms for cell-type-specific Sox2 neuronal and glial functions. SOX2 mutations in humans lead to a spectrum of nervous system defects, involving vision, movement control, and cognition; the identification of neurons and glia requiring Sox2 function, and the investigation of Sox2 roles and molecular targets within them, represents a novel perspective for the understanding of the pathogenesis of these defects.</description><subject>Abnormalities</subject><subject>Animals</subject><subject>Astrocytes</subject><subject>Ataxia</subject><subject>Basal ganglia</subject><subject>Binding sites</subject><subject>Cell adhesion & migration</subject><subject>Cell Differentiation</subject><subject>Cell Self Renewal</subject><subject>Clonal deletion</subject><subject>Defects</subject><subject>Down-Regulation</subject><subject>Embryogenesis</subject><subject>Enhancers</subject><subject>Epigenetics</subject><subject>Forebrain</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Glial cells</subject><subject>Hippocampus</subject><subject>Humans</subject><subject>Intellectual disabilities</subject><subject>Mice</subject><subject>Morphology</subject><subject>Motor task performance</subject><subject>Mutants</subject><subject>Mutation</subject><subject>Nervous system</subject><subject>Neural Stem Cells - cytology</subject><subject>Neural Stem Cells - metabolism</subject><subject>Neurodevelopmental disorders</subject><subject>Neurogenesis</subject><subject>Neuroglia - cytology</subject><subject>Neuroglia - metabolism</subject><subject>Neuronal-glial interactions</subject><subject>Phenotypes</subject><subject>Primordia</subject><subject>Radial glial cells</subject><subject>Review</subject><subject>Roles</subject><subject>Seizures</subject><subject>Signal Transduction</subject><subject>SOXB1 Transcription Factors - genetics</subject><subject>SOXB1 Transcription Factors - metabolism</subject><subject>Stem cells</subject><subject>Substantia alba</subject><subject>Thyroid transcription factor 1</subject><subject>Transcription factors</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkUFvEzEQhS1ERUvhxhlZ4sKBtLbH693lgIQCSSsVkEg4W453ljratVPbi8q_x1XaKvQ0I82npzfvEfKGszOAlp277ZgE442sJHtGTrgUYsaYqp8f7MfkZUpbxgSIqn1BjoEXWKj2hIRvISLN18bT7ZQyXWUc6RyHIX2ki8nb7II3A_0ZBkw09IVEuo7GJxvd7u5IF8bmEOkq3ArqPP3i-h4j-uxMxo4uB2eo8R39jlMMPr0iR70ZEr6-n6fk1-Lren4xu_qxvJx_vppZWTd5JjoBrAPFxUbUyPrOGJByA5UU2HebtgJVqaayyJg0VilZt7znILBtmg55Bafk0153N21G7GwxFM2gd9GNJv7VwTj9_8W7a_07_NGqVm3NmiLw_l4ghpsJU9ajS7YEYzyGKWkh2ko2AJIX9N0TdBumWGIrFAA0Qha7hfqwp2wMKUXsH81wpu-a1IdNFvzt4QOP8EN18A_41ZnP</recordid><startdate>20190913</startdate><enddate>20190913</enddate><creator>Mercurio, Sara</creator><creator>Serra, Linda</creator><creator>Nicolis, Silvia K</creator><general>MDPI AG</general><general>MDPI</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190913</creationdate><title>More than just Stem Cells: Functional Roles of the Transcription Factor Sox2 in Differentiated Glia and Neurons</title><author>Mercurio, Sara ; Serra, Linda ; Nicolis, Silvia K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c478t-2d230d3612b27e0fdaa344b3542efdb95365685ce004ac664791f132e988de153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Abnormalities</topic><topic>Animals</topic><topic>Astrocytes</topic><topic>Ataxia</topic><topic>Basal ganglia</topic><topic>Binding sites</topic><topic>Cell adhesion & migration</topic><topic>Cell Differentiation</topic><topic>Cell Self Renewal</topic><topic>Clonal deletion</topic><topic>Defects</topic><topic>Down-Regulation</topic><topic>Embryogenesis</topic><topic>Enhancers</topic><topic>Epigenetics</topic><topic>Forebrain</topic><topic>Gene expression</topic><topic>Genes</topic><topic>Glial cells</topic><topic>Hippocampus</topic><topic>Humans</topic><topic>Intellectual disabilities</topic><topic>Mice</topic><topic>Morphology</topic><topic>Motor task performance</topic><topic>Mutants</topic><topic>Mutation</topic><topic>Nervous system</topic><topic>Neural Stem Cells - cytology</topic><topic>Neural Stem Cells - metabolism</topic><topic>Neurodevelopmental disorders</topic><topic>Neurogenesis</topic><topic>Neuroglia - cytology</topic><topic>Neuroglia - metabolism</topic><topic>Neuronal-glial interactions</topic><topic>Phenotypes</topic><topic>Primordia</topic><topic>Radial glial cells</topic><topic>Review</topic><topic>Roles</topic><topic>Seizures</topic><topic>Signal Transduction</topic><topic>SOXB1 Transcription Factors - genetics</topic><topic>SOXB1 Transcription Factors - metabolism</topic><topic>Stem cells</topic><topic>Substantia alba</topic><topic>Thyroid transcription factor 1</topic><topic>Transcription factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mercurio, Sara</creatorcontrib><creatorcontrib>Serra, Linda</creatorcontrib><creatorcontrib>Nicolis, Silvia K</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mercurio, Sara</au><au>Serra, Linda</au><au>Nicolis, Silvia K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>More than just Stem Cells: Functional Roles of the Transcription Factor Sox2 in Differentiated Glia and Neurons</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2019-09-13</date><risdate>2019</risdate><volume>20</volume><issue>18</issue><spage>4540</spage><pages>4540-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>The Sox2 transcription factor, encoded by a gene conserved in animal evolution, has become widely known because of its functional relevance for stem cells. In the developing nervous system, Sox2 is active in neural stem cells, and important for their self-renewal; differentiation to neurons and glia normally involves Sox2 downregulation. Recent evidence, however, identified specific types of fully differentiated neurons and glia that retain high Sox2 expression, and critically require Sox2 function, as revealed by functional studies in mouse and in other animals. Sox2 was found to control fundamental aspects of the biology of these cells, such as the development of correct neuronal connectivity. Sox2 downstream target genes identified within these cell types provide molecular mechanisms for cell-type-specific Sox2 neuronal and glial functions. SOX2 mutations in humans lead to a spectrum of nervous system defects, involving vision, movement control, and cognition; the identification of neurons and glia requiring Sox2 function, and the investigation of Sox2 roles and molecular targets within them, represents a novel perspective for the understanding of the pathogenesis of these defects.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>31540269</pmid><doi>10.3390/ijms20184540</doi><oa>free_for_read</oa></addata></record> |
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subjects | Abnormalities Animals Astrocytes Ataxia Basal ganglia Binding sites Cell adhesion & migration Cell Differentiation Cell Self Renewal Clonal deletion Defects Down-Regulation Embryogenesis Enhancers Epigenetics Forebrain Gene expression Genes Glial cells Hippocampus Humans Intellectual disabilities Mice Morphology Motor task performance Mutants Mutation Nervous system Neural Stem Cells - cytology Neural Stem Cells - metabolism Neurodevelopmental disorders Neurogenesis Neuroglia - cytology Neuroglia - metabolism Neuronal-glial interactions Phenotypes Primordia Radial glial cells Review Roles Seizures Signal Transduction SOXB1 Transcription Factors - genetics SOXB1 Transcription Factors - metabolism Stem cells Substantia alba Thyroid transcription factor 1 Transcription factors |
title | More than just Stem Cells: Functional Roles of the Transcription Factor Sox2 in Differentiated Glia and Neurons |
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