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Folate deficiency prevents neural crest fate by disturbing the epigenetic Sox2 repression on the dorsal neural tube
Folate deficiency has been known to contribute to neural tube and neural crest defects, but why these tissues are particularly affected, and which are the molecular mechanisms involved in those abnormalities are important human health questions that remain unanswered. Here we study the function of t...
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Published in: | Developmental biology 2018-12, Vol.444, p.S193-S201 |
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creator | Alata Jimenez, Nagif Torres Pérez, Sergio A. Sánchez-Vásquez, Estefanía Fernandino, Juan I. Strobl-Mazzulla, Pablo H. |
description | Folate deficiency has been known to contribute to neural tube and neural crest defects, but why these tissues are particularly affected, and which are the molecular mechanisms involved in those abnormalities are important human health questions that remain unanswered. Here we study the function of two of the main folate transporters, FolR1 and Rfc1, which are robustly expressed in these tissues. Folate is the precursor of S-adenosylmethionine, which is the main donor for DNA, protein and RNA methylation. Our results show that knockdown of FolR1 and/or Rfc1 reduced the abundance of histone H3 lysine and DNA methylation, two epigenetic modifications that play an important role during neural and neural crest development. Additionally, by knocking down folate transporter or pharmacologically inhibiting folate transport and metabolism, we observed ectopic Sox2 expression at the expense of neural crest markers in the dorsal neural tube. This is correlated with neural crest associated defects, with particular impact on orofacial formation. By using bisulfite sequencing, we show that this phenotype is consequence of reduced DNA methylation on the Sox2 locus at the dorsal neural tube, which can be rescued by the addition of folinic acid. Taken together, our in vivo results reveal the importance of folate as a source of the methyl groups necessary for the establishment of the correct epigenetic marks during neural and neural crest fate-restriction.
•The epigenetic mechanism of folate deficiency on orofacial anomalies is presented.•Loss of folate transporters confers neural fate to the dorsal neural tube progenitors.•Folate transporter are required for epigenetic Sox2 repression on neural crest territory. |
doi_str_mv | 10.1016/j.ydbio.2018.08.001 |
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•The epigenetic mechanism of folate deficiency on orofacial anomalies is presented.•Loss of folate transporters confers neural fate to the dorsal neural tube progenitors.•Folate transporter are required for epigenetic Sox2 repression on neural crest territory.</description><subject>DNA methylation</subject><subject>Epigenetic</subject><subject>Folate</subject><subject>Neural crest</subject><subject>Sox2</subject><issn>0012-1606</issn><issn>1095-564X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kM1rGzEQxUVpaFy3f0Gh6NjLuqP9lA49hBCngUAOSSA3oY9ZV2a9ciVtqP_7aGM3x8CDgeE37zGPkG8MVgxY-3O7Oljt_KoExleQBewDWTAQTdG09dNHssibsmAttOfkc4xbAKg4rz6R8wpAcCHEgsS1H1RCarF3xuFoDnQf8BnHFOmIU1ADNQFjov1M6QO1LqYpaDduaPqDFPdugyMmZ-i9_1fSgPk8RudHmjUT1oeYXU5madL4hZz1aoj49TSX5HF99XD5u7i9u765vLgtTA11KgzrtGLIoe5tYzkTSuua1X3XtKIxHfBaqLLtRIdgmBaqqUxZKWVM0_OmLlm1JD-Ovvvg_075Cblz0eAwqBH9FGUJvBOi4qXIaHVETfAxBuzlPridCgfJQM5ty618bVvObUvIgjng-ylg0ju0bzf_683AryOA-c1nh0HG15LRuoAmSevduwEvTxSTYQ</recordid><startdate>20181201</startdate><enddate>20181201</enddate><creator>Alata Jimenez, Nagif</creator><creator>Torres Pérez, Sergio A.</creator><creator>Sánchez-Vásquez, Estefanía</creator><creator>Fernandino, Juan I.</creator><creator>Strobl-Mazzulla, Pablo H.</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6585-8548</orcidid></search><sort><creationdate>20181201</creationdate><title>Folate deficiency prevents neural crest fate by disturbing the epigenetic Sox2 repression on the dorsal neural tube</title><author>Alata Jimenez, Nagif ; Torres Pérez, Sergio A. ; Sánchez-Vásquez, Estefanía ; Fernandino, Juan I. ; Strobl-Mazzulla, Pablo H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-c17ba1e804fd5d819abb414f75695c70849a26797e0c1b9a53c23aacc5f854213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>DNA methylation</topic><topic>Epigenetic</topic><topic>Folate</topic><topic>Neural crest</topic><topic>Sox2</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alata Jimenez, Nagif</creatorcontrib><creatorcontrib>Torres Pérez, Sergio A.</creatorcontrib><creatorcontrib>Sánchez-Vásquez, Estefanía</creatorcontrib><creatorcontrib>Fernandino, Juan I.</creatorcontrib><creatorcontrib>Strobl-Mazzulla, Pablo H.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Developmental biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alata Jimenez, Nagif</au><au>Torres Pérez, Sergio A.</au><au>Sánchez-Vásquez, Estefanía</au><au>Fernandino, Juan I.</au><au>Strobl-Mazzulla, Pablo H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Folate deficiency prevents neural crest fate by disturbing the epigenetic Sox2 repression on the dorsal neural tube</atitle><jtitle>Developmental biology</jtitle><addtitle>Dev Biol</addtitle><date>2018-12-01</date><risdate>2018</risdate><volume>444</volume><spage>S193</spage><epage>S201</epage><pages>S193-S201</pages><issn>0012-1606</issn><eissn>1095-564X</eissn><abstract>Folate deficiency has been known to contribute to neural tube and neural crest defects, but why these tissues are particularly affected, and which are the molecular mechanisms involved in those abnormalities are important human health questions that remain unanswered. Here we study the function of two of the main folate transporters, FolR1 and Rfc1, which are robustly expressed in these tissues. Folate is the precursor of S-adenosylmethionine, which is the main donor for DNA, protein and RNA methylation. Our results show that knockdown of FolR1 and/or Rfc1 reduced the abundance of histone H3 lysine and DNA methylation, two epigenetic modifications that play an important role during neural and neural crest development. Additionally, by knocking down folate transporter or pharmacologically inhibiting folate transport and metabolism, we observed ectopic Sox2 expression at the expense of neural crest markers in the dorsal neural tube. This is correlated with neural crest associated defects, with particular impact on orofacial formation. By using bisulfite sequencing, we show that this phenotype is consequence of reduced DNA methylation on the Sox2 locus at the dorsal neural tube, which can be rescued by the addition of folinic acid. Taken together, our in vivo results reveal the importance of folate as a source of the methyl groups necessary for the establishment of the correct epigenetic marks during neural and neural crest fate-restriction.
•The epigenetic mechanism of folate deficiency on orofacial anomalies is presented.•Loss of folate transporters confers neural fate to the dorsal neural tube progenitors.•Folate transporter are required for epigenetic Sox2 repression on neural crest territory.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30098999</pmid><doi>10.1016/j.ydbio.2018.08.001</doi><orcidid>https://orcid.org/0000-0002-6585-8548</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | DNA methylation Epigenetic Folate Neural crest Sox2 |
title | Folate deficiency prevents neural crest fate by disturbing the epigenetic Sox2 repression on the dorsal neural tube |
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