Transcription factor TEAD1 is essential for vascular development by promoting vascular smooth muscle differentiation
TEAD1 (TEA domain transcription factor 1), a transcription factor known for the functional output of Hippo signaling, is important for tumorigenesis. However, the role of TEAD1 in the development of vascular smooth muscle cell (VSMC) is unknown. To investigate cell-specific role of Tead1 , we genera...
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Veröffentlicht in: | Cell death and differentiation 2019-12, Vol.26 (12), p.2790-2806 |
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creator | Wen, Tong Liu, Jinhua He, Xiangqin Dong, Kunzhe Hu, Guoqing Yu, Luyi Yin, Qin Osman, Islam Peng, Jingtian Zheng, Zeqi Xin, Hongbo Fulton, David Du, Quansheng Zhang, Wei Zhou, Jiliang |
description | TEAD1 (TEA domain transcription factor 1), a transcription factor known for the functional output of Hippo signaling, is important for tumorigenesis. However, the role of TEAD1 in the development of vascular smooth muscle cell (VSMC) is unknown. To investigate cell-specific role of
Tead1
, we generated cardiomyocyte (CMC) and VSMC-specific
Tead1
knockout mice. We found CMC/VSMC-specific deletion of
Tead1
led to embryonic lethality by E14.5 in mice due to hypoplastic cardiac and vascular walls, as a result of impaired CMC and VSMC proliferation. Whole transcriptome analysis revealed that deletion of
Tead1
in CMCs/VSMCs downregulated expression of muscle contractile genes and key transcription factors including
Pitx2c
and myocardin. In vitro studies demonstrated that PITX2c and myocardin rescued TEAD1-dependent defects in VSMC differentiation. We further identified
Pitx2c
as a novel transcriptional target of TEAD1, and PITX2c exhibited functional synergy with myocardin by directly interacting with myocardin, leading to augment the differentiation of VSMC. In summary, our study reveals a critical role of
Tead1
in cardiovascular development in mice, but also identifies a novel regulatory mechanism, whereby
Tead1
functions upstream of the genetic regulatory hierarchy for establishing smooth muscle contractile phenotype. |
doi_str_mv | 10.1038/s41418-019-0335-4 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7224394</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2314311258</sourcerecordid><originalsourceid>FETCH-LOGICAL-c470t-4427ad907e7ac1778b58afd79e8bbd42c9076a3b3107b371cba4f0518b39724e3</originalsourceid><addsrcrecordid>eNp1kV1LwzAYhYMobk5_gDcS8Lqary7tjTDm_ICBN_M6JGm6ZbRNTdrB_r2Zm1MvvErIOXnO-3IAuMboDiOa3QeGGc4ShPMEUZom7AQMMePjJGWInsY7TVGSI8YH4CKENUJozPPxORhQjAhDPB2CbuFlE7S3bWddA0upO-fhYjZ5xNAGaEIwTWdlBcv4vJFB95X0sDAbU7m2jhpUW9h6V7vONssfR6id61aw7oOuDCxsWRr_RdrFXIKzUlbBXB3OEXh_mi2mL8n87fl1OpknmnHUJYwRLoscccOlxpxnKs1kWfDcZEoVjOgojSVVcRuuKMdaSVaiFGeK5pwwQ0fgYc9te1WbQscBvKxE620t_VY4acVfpbErsXQbwQlhNGcRcHsAePfRm9CJtet9E2cWhGJGMSZpFl1479LeheBNeUzASOyKEvuiRCxK7IoSO_LN79GOP76biQayN4QoNUvjf6L_p34Cis6hUg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2314311258</pqid></control><display><type>article</type><title>Transcription factor TEAD1 is essential for vascular development by promoting vascular smooth muscle differentiation</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Wen, Tong ; Liu, Jinhua ; He, Xiangqin ; Dong, Kunzhe ; Hu, Guoqing ; Yu, Luyi ; Yin, Qin ; Osman, Islam ; Peng, Jingtian ; Zheng, Zeqi ; Xin, Hongbo ; Fulton, David ; Du, Quansheng ; Zhang, Wei ; Zhou, Jiliang</creator><creatorcontrib>Wen, Tong ; Liu, Jinhua ; He, Xiangqin ; Dong, Kunzhe ; Hu, Guoqing ; Yu, Luyi ; Yin, Qin ; Osman, Islam ; Peng, Jingtian ; Zheng, Zeqi ; Xin, Hongbo ; Fulton, David ; Du, Quansheng ; Zhang, Wei ; Zhou, Jiliang</creatorcontrib><description>TEAD1 (TEA domain transcription factor 1), a transcription factor known for the functional output of Hippo signaling, is important for tumorigenesis. However, the role of TEAD1 in the development of vascular smooth muscle cell (VSMC) is unknown. To investigate cell-specific role of
Tead1
, we generated cardiomyocyte (CMC) and VSMC-specific
Tead1
knockout mice. We found CMC/VSMC-specific deletion of
Tead1
led to embryonic lethality by E14.5 in mice due to hypoplastic cardiac and vascular walls, as a result of impaired CMC and VSMC proliferation. Whole transcriptome analysis revealed that deletion of
Tead1
in CMCs/VSMCs downregulated expression of muscle contractile genes and key transcription factors including
Pitx2c
and myocardin. In vitro studies demonstrated that PITX2c and myocardin rescued TEAD1-dependent defects in VSMC differentiation. We further identified
Pitx2c
as a novel transcriptional target of TEAD1, and PITX2c exhibited functional synergy with myocardin by directly interacting with myocardin, leading to augment the differentiation of VSMC. In summary, our study reveals a critical role of
Tead1
in cardiovascular development in mice, but also identifies a novel regulatory mechanism, whereby
Tead1
functions upstream of the genetic regulatory hierarchy for establishing smooth muscle contractile phenotype.</description><identifier>ISSN: 1350-9047</identifier><identifier>EISSN: 1476-5403</identifier><identifier>DOI: 10.1038/s41418-019-0335-4</identifier><identifier>PMID: 31024075</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/44 ; 14/19 ; 14/35 ; 14/63 ; 631/208/135 ; 631/208/200 ; 64/60 ; 96/109 ; 96/31 ; Animals ; Apoptosis ; Biochemistry ; Biomedical and Life Sciences ; Cardiomyocytes ; Cell Biology ; Cell Cycle Analysis ; Cell Differentiation - physiology ; Clonal deletion ; DNA-Binding Proteins - genetics ; DNA-Binding Proteins - metabolism ; Embryos ; Female ; Gene Deletion ; Gene expression ; Lethality ; Life Sciences ; Male ; Mice ; Mice, Knockout ; Muscle contraction ; Muscle, Smooth, Vascular - cytology ; Muscle, Smooth, Vascular - growth & development ; Muscle, Smooth, Vascular - metabolism ; Phenotypes ; Smooth muscle ; Stem Cells ; TEA Domain Transcription Factors ; Transcription factors ; Transcription Factors - genetics ; Transcription Factors - metabolism ; Tumorigenesis</subject><ispartof>Cell death and differentiation, 2019-12, Vol.26 (12), p.2790-2806</ispartof><rights>ADMC Associazione Differenziamento e Morte Cellulare 2019</rights><rights>ADMC Associazione Differenziamento e Morte Cellulare 2019.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-4427ad907e7ac1778b58afd79e8bbd42c9076a3b3107b371cba4f0518b39724e3</citedby><cites>FETCH-LOGICAL-c470t-4427ad907e7ac1778b58afd79e8bbd42c9076a3b3107b371cba4f0518b39724e3</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/PMC7224394/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7224394/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,41464,42533,51294,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31024075$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wen, Tong</creatorcontrib><creatorcontrib>Liu, Jinhua</creatorcontrib><creatorcontrib>He, Xiangqin</creatorcontrib><creatorcontrib>Dong, Kunzhe</creatorcontrib><creatorcontrib>Hu, Guoqing</creatorcontrib><creatorcontrib>Yu, Luyi</creatorcontrib><creatorcontrib>Yin, Qin</creatorcontrib><creatorcontrib>Osman, Islam</creatorcontrib><creatorcontrib>Peng, Jingtian</creatorcontrib><creatorcontrib>Zheng, Zeqi</creatorcontrib><creatorcontrib>Xin, Hongbo</creatorcontrib><creatorcontrib>Fulton, David</creatorcontrib><creatorcontrib>Du, Quansheng</creatorcontrib><creatorcontrib>Zhang, Wei</creatorcontrib><creatorcontrib>Zhou, Jiliang</creatorcontrib><title>Transcription factor TEAD1 is essential for vascular development by promoting vascular smooth muscle differentiation</title><title>Cell death and differentiation</title><addtitle>Cell Death Differ</addtitle><addtitle>Cell Death Differ</addtitle><description>TEAD1 (TEA domain transcription factor 1), a transcription factor known for the functional output of Hippo signaling, is important for tumorigenesis. However, the role of TEAD1 in the development of vascular smooth muscle cell (VSMC) is unknown. To investigate cell-specific role of
Tead1
, we generated cardiomyocyte (CMC) and VSMC-specific
Tead1
knockout mice. We found CMC/VSMC-specific deletion of
Tead1
led to embryonic lethality by E14.5 in mice due to hypoplastic cardiac and vascular walls, as a result of impaired CMC and VSMC proliferation. Whole transcriptome analysis revealed that deletion of
Tead1
in CMCs/VSMCs downregulated expression of muscle contractile genes and key transcription factors including
Pitx2c
and myocardin. In vitro studies demonstrated that PITX2c and myocardin rescued TEAD1-dependent defects in VSMC differentiation. We further identified
Pitx2c
as a novel transcriptional target of TEAD1, and PITX2c exhibited functional synergy with myocardin by directly interacting with myocardin, leading to augment the differentiation of VSMC. In summary, our study reveals a critical role of
Tead1
in cardiovascular development in mice, but also identifies a novel regulatory mechanism, whereby
Tead1
functions upstream of the genetic regulatory hierarchy for establishing smooth muscle contractile phenotype.</description><subject>13/44</subject><subject>14/19</subject><subject>14/35</subject><subject>14/63</subject><subject>631/208/135</subject><subject>631/208/200</subject><subject>64/60</subject><subject>96/109</subject><subject>96/31</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Cardiomyocytes</subject><subject>Cell Biology</subject><subject>Cell Cycle Analysis</subject><subject>Cell Differentiation - physiology</subject><subject>Clonal deletion</subject><subject>DNA-Binding Proteins - genetics</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Embryos</subject><subject>Female</subject><subject>Gene Deletion</subject><subject>Gene expression</subject><subject>Lethality</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Muscle contraction</subject><subject>Muscle, Smooth, Vascular - cytology</subject><subject>Muscle, Smooth, Vascular - growth & development</subject><subject>Muscle, Smooth, Vascular - metabolism</subject><subject>Phenotypes</subject><subject>Smooth muscle</subject><subject>Stem Cells</subject><subject>TEA Domain Transcription Factors</subject><subject>Transcription factors</subject><subject>Transcription Factors - genetics</subject><subject>Transcription Factors - metabolism</subject><subject>Tumorigenesis</subject><issn>1350-9047</issn><issn>1476-5403</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kV1LwzAYhYMobk5_gDcS8Lqary7tjTDm_ICBN_M6JGm6ZbRNTdrB_r2Zm1MvvErIOXnO-3IAuMboDiOa3QeGGc4ShPMEUZom7AQMMePjJGWInsY7TVGSI8YH4CKENUJozPPxORhQjAhDPB2CbuFlE7S3bWddA0upO-fhYjZ5xNAGaEIwTWdlBcv4vJFB95X0sDAbU7m2jhpUW9h6V7vONssfR6id61aw7oOuDCxsWRr_RdrFXIKzUlbBXB3OEXh_mi2mL8n87fl1OpknmnHUJYwRLoscccOlxpxnKs1kWfDcZEoVjOgojSVVcRuuKMdaSVaiFGeK5pwwQ0fgYc9te1WbQscBvKxE620t_VY4acVfpbErsXQbwQlhNGcRcHsAePfRm9CJtet9E2cWhGJGMSZpFl1479LeheBNeUzASOyKEvuiRCxK7IoSO_LN79GOP76biQayN4QoNUvjf6L_p34Cis6hUg</recordid><startdate>20191201</startdate><enddate>20191201</enddate><creator>Wen, Tong</creator><creator>Liu, Jinhua</creator><creator>He, Xiangqin</creator><creator>Dong, Kunzhe</creator><creator>Hu, Guoqing</creator><creator>Yu, Luyi</creator><creator>Yin, Qin</creator><creator>Osman, Islam</creator><creator>Peng, Jingtian</creator><creator>Zheng, Zeqi</creator><creator>Xin, Hongbo</creator><creator>Fulton, David</creator><creator>Du, Quansheng</creator><creator>Zhang, Wei</creator><creator>Zhou, Jiliang</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</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>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20191201</creationdate><title>Transcription factor TEAD1 is essential for vascular development by promoting vascular smooth muscle differentiation</title><author>Wen, Tong ; Liu, Jinhua ; He, Xiangqin ; Dong, Kunzhe ; Hu, Guoqing ; Yu, Luyi ; Yin, Qin ; Osman, Islam ; Peng, Jingtian ; Zheng, Zeqi ; Xin, Hongbo ; Fulton, David ; Du, Quansheng ; Zhang, Wei ; Zhou, Jiliang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-4427ad907e7ac1778b58afd79e8bbd42c9076a3b3107b371cba4f0518b39724e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>13/44</topic><topic>14/19</topic><topic>14/35</topic><topic>14/63</topic><topic>631/208/135</topic><topic>631/208/200</topic><topic>64/60</topic><topic>96/109</topic><topic>96/31</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Cardiomyocytes</topic><topic>Cell Biology</topic><topic>Cell Cycle Analysis</topic><topic>Cell Differentiation - physiology</topic><topic>Clonal deletion</topic><topic>DNA-Binding Proteins - genetics</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Embryos</topic><topic>Female</topic><topic>Gene Deletion</topic><topic>Gene expression</topic><topic>Lethality</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Muscle contraction</topic><topic>Muscle, Smooth, Vascular - cytology</topic><topic>Muscle, Smooth, Vascular - growth & development</topic><topic>Muscle, Smooth, Vascular - metabolism</topic><topic>Phenotypes</topic><topic>Smooth muscle</topic><topic>Stem Cells</topic><topic>TEA Domain Transcription Factors</topic><topic>Transcription factors</topic><topic>Transcription Factors - genetics</topic><topic>Transcription Factors - metabolism</topic><topic>Tumorigenesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wen, Tong</creatorcontrib><creatorcontrib>Liu, Jinhua</creatorcontrib><creatorcontrib>He, Xiangqin</creatorcontrib><creatorcontrib>Dong, Kunzhe</creatorcontrib><creatorcontrib>Hu, Guoqing</creatorcontrib><creatorcontrib>Yu, Luyi</creatorcontrib><creatorcontrib>Yin, Qin</creatorcontrib><creatorcontrib>Osman, Islam</creatorcontrib><creatorcontrib>Peng, Jingtian</creatorcontrib><creatorcontrib>Zheng, Zeqi</creatorcontrib><creatorcontrib>Xin, Hongbo</creatorcontrib><creatorcontrib>Fulton, David</creatorcontrib><creatorcontrib>Du, Quansheng</creatorcontrib><creatorcontrib>Zhang, Wei</creatorcontrib><creatorcontrib>Zhou, Jiliang</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>Calcium & Calcified Tissue 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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>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cell death and differentiation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wen, Tong</au><au>Liu, Jinhua</au><au>He, Xiangqin</au><au>Dong, Kunzhe</au><au>Hu, Guoqing</au><au>Yu, Luyi</au><au>Yin, Qin</au><au>Osman, Islam</au><au>Peng, Jingtian</au><au>Zheng, Zeqi</au><au>Xin, Hongbo</au><au>Fulton, David</au><au>Du, Quansheng</au><au>Zhang, Wei</au><au>Zhou, Jiliang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transcription factor TEAD1 is essential for vascular development by promoting vascular smooth muscle differentiation</atitle><jtitle>Cell death and differentiation</jtitle><stitle>Cell Death Differ</stitle><addtitle>Cell Death Differ</addtitle><date>2019-12-01</date><risdate>2019</risdate><volume>26</volume><issue>12</issue><spage>2790</spage><epage>2806</epage><pages>2790-2806</pages><issn>1350-9047</issn><eissn>1476-5403</eissn><abstract>TEAD1 (TEA domain transcription factor 1), a transcription factor known for the functional output of Hippo signaling, is important for tumorigenesis. However, the role of TEAD1 in the development of vascular smooth muscle cell (VSMC) is unknown. To investigate cell-specific role of
Tead1
, we generated cardiomyocyte (CMC) and VSMC-specific
Tead1
knockout mice. We found CMC/VSMC-specific deletion of
Tead1
led to embryonic lethality by E14.5 in mice due to hypoplastic cardiac and vascular walls, as a result of impaired CMC and VSMC proliferation. Whole transcriptome analysis revealed that deletion of
Tead1
in CMCs/VSMCs downregulated expression of muscle contractile genes and key transcription factors including
Pitx2c
and myocardin. In vitro studies demonstrated that PITX2c and myocardin rescued TEAD1-dependent defects in VSMC differentiation. We further identified
Pitx2c
as a novel transcriptional target of TEAD1, and PITX2c exhibited functional synergy with myocardin by directly interacting with myocardin, leading to augment the differentiation of VSMC. In summary, our study reveals a critical role of
Tead1
in cardiovascular development in mice, but also identifies a novel regulatory mechanism, whereby
Tead1
functions upstream of the genetic regulatory hierarchy for establishing smooth muscle contractile phenotype.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>31024075</pmid><doi>10.1038/s41418-019-0335-4</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Springer Nature - Complete Springer Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | 13/44 14/19 14/35 14/63 631/208/135 631/208/200 64/60 96/109 96/31 Animals Apoptosis Biochemistry Biomedical and Life Sciences Cardiomyocytes Cell Biology Cell Cycle Analysis Cell Differentiation - physiology Clonal deletion DNA-Binding Proteins - genetics DNA-Binding Proteins - metabolism Embryos Female Gene Deletion Gene expression Lethality Life Sciences Male Mice Mice, Knockout Muscle contraction Muscle, Smooth, Vascular - cytology Muscle, Smooth, Vascular - growth & development Muscle, Smooth, Vascular - metabolism Phenotypes Smooth muscle Stem Cells TEA Domain Transcription Factors Transcription factors Transcription Factors - genetics Transcription Factors - metabolism Tumorigenesis |
title | Transcription factor TEAD1 is essential for vascular development by promoting vascular smooth muscle differentiation |
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