<?xml version="1.0" ?>
<!DOCTYPE PubmedArticleSet PUBLIC "-//NLM//DTD PubMedArticle, 1st January 2025//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/out/pubmed_250101.dtd">
<PubmedArticleSet>
<PubmedArticle><MedlineCitation Status="MEDLINE" Owner="NLM" IndexingMethod="Manual"><PMID Version="1">21852402</PMID><DateCompleted><Year>2011</Year><Month>11</Month><Day>22</Day></DateCompleted><DateRevised><Year>2021</Year><Month>10</Month><Day>20</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1477-9129</ISSN><JournalIssue CitedMedium="Internet"><Volume>138</Volume><Issue>19</Issue><PubDate><Year>2011</Year><Month>Oct</Month></PubDate></JournalIssue><Title>Development (Cambridge, England)</Title><ISOAbbreviation>Development</ISOAbbreviation></Journal><ArticleTitle>Fez function is required to maintain the size of the animal plate in the sea urchin embryo.</ArticleTitle><Pagination><StartPage>4233</StartPage><EndPage>4243</EndPage><MedlinePgn>4233-43</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1242/dev.069856</ELocationID><Abstract><AbstractText>Partitioning ectoderm precisely into neurogenic and non-neurogenic regions is an essential step for neurogenesis of almost all bilaterian embryos. Although it is widely accepted that antagonism between BMP and its inhibitors primarily sets up the border between these two types of ectoderm, it is unclear how such extracellular, diffusible molecules create a sharp and precise border at the single-cell level. Here, we show that Fez, a zinc finger protein, functions as an intracellular factor attenuating BMP signaling specifically within the neurogenic region at the anterior end of sea urchin embryos, termed the animal plate. When Fez function is blocked, the size of this neurogenic ectoderm becomes smaller than normal. However, this reduction is rescued in Fez morphants simply by blocking BMP2/4 translation, indicating that Fez maintains the size of the animal plate by attenuating BMP2/4 function. Consistent with this, the gradient of BMP activity along the aboral side of the animal plate, as measured by pSmad1/5/8 levels, drops significantly in cells expressing Fez and this steep decline requires Fez function. Our data reveal that this neurogenic ectoderm produces an intrinsic system that attenuates BMP signaling to ensure the establishment of a stable, well-defined neural territory, the animal plate.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Yaguchi</LastName><ForeName>Shunsuke</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>Shimoda Marine Research Center, University of Tsukuba, 5-10-1 Shimoda, Shizuoka 415-0025, Japan. yag@kurofune.shimoda.tsukuba.ac.jp</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Yaguchi</LastName><ForeName>Junko</ForeName><Initials>J</Initials></Author><Author ValidYN="Y"><LastName>Wei</LastName><ForeName>Zheng</ForeName><Initials>Z</Initials></Author><Author ValidYN="Y"><LastName>Jin</LastName><ForeName>Yinhua</ForeName><Initials>Y</Initials></Author><Author ValidYN="Y"><LastName>Angerer</LastName><ForeName>Lynne M</ForeName><Initials>LM</Initials></Author><Author ValidYN="Y"><LastName>Inaba</LastName><ForeName>Kazuo</ForeName><Initials>K</Initials></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><Agency>Intramural NIH HHS</Agency><Country>United States</Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D052060">Research Support, N.I.H., Intramural</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2011</Year><Month>08</Month><Day>18</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Development</MedlineTA><NlmUniqueID>8701744</NlmUniqueID><ISSNLinking>0950-1991</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D019485">Bone Morphogenetic Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D051785">Smad Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D014157">Transcription Factors</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D036703" MajorTopicYN="N">Blastula</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D019521" MajorTopicYN="N">Body Patterning</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D019485" MajorTopicYN="N">Bone Morphogenetic Proteins</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D019070" MajorTopicYN="N">Cell Lineage</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004475" MajorTopicYN="N">Ectoderm</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D004625" MajorTopicYN="N">Embryo, Nonmammalian</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018507" MajorTopicYN="Y">Gene Expression Regulation, Developmental</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D007150" MajorTopicYN="N">Immunohistochemistry</DescriptorName><QualifierName UI="Q000379" MajorTopicYN="N">methods</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008954" MajorTopicYN="N">Models, Biological</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009693" MajorTopicYN="N">Nucleic Acid Hybridization</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D020411" MajorTopicYN="N">Oligonucleotide Array Sequence Analysis</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012617" MajorTopicYN="N">Sea Urchins</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D051785" MajorTopicYN="N">Smad Proteins</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014157" MajorTopicYN="N">Transcription Factors</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D016335" MajorTopicYN="Y">Zinc Fingers</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2011</Year><Month>8</Month><Day>20</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2011</Year><Month>8</Month><Day>20</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2011</Year><Month>12</Month><Day>13</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pmc-release"><Year>2012</Year><Month>10</Month><Day>1</Day></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">21852402</ArticleId><ArticleId IdType="pmc">PMC3171223</ArticleId><ArticleId IdType="doi">10.1242/dev.069856</ArticleId><ArticleId IdType="pii">dev.069856</ArticleId></ArticleIdList><ReferenceList><Reference><Citation>
Alexandrova E. M., Thomsen G. H. (2006). Smurf1 regulates neural patterning and folding in <i>Xenopus</i> embryos by antagonizing the BMP/Smad1 pathway. <i>Dev. Biol.</i> 299, 398-410
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC2577174</ArticleId><ArticleId IdType="pubmed">16973150</ArticleId></ArticleIdList></Reference><Reference><Citation>
Angerer L. M., Oleksyn D. W., Logan C. Y., McClay D. R., Dale L., Angerer R. C. (2000). A BMP pathway regulates cell fate allocation along the sea urchin animal-vegetal embryonic axis. <i>Development</i> 127, 1105-1114
</Citation><ArticleIdList><ArticleId IdType="pubmed">10662649</ArticleId></ArticleIdList></Reference><Reference><Citation>
Ben-Zvi D., Shilo B. Z., Fainsod A., Barkai N. (2008). Scaling of the BMP activation gradient in <i>Xenopus</i> embryos. <i>Nature</i> 453, 1205-1211
</Citation><ArticleIdList><ArticleId IdType="pubmed">18580943</ArticleId></ArticleIdList></Reference><Reference><Citation>
Bradham C. A., Oikonomou C., Kuhn A., Core A. B., Modell J. W., McClay D. R., Poustka A. J. (2009). Chordin is required for neural but not axial development in sea urchin embryos. <i>Dev. Biol.</i> 328, 221-233
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC2700341</ArticleId><ArticleId IdType="pubmed">19389361</ArticleId></ArticleIdList></Reference><Reference><Citation>
Burke R. D., Osborne L., Wang D., Murabe N., Yaguchi S., Nakajima Y. (2006). Neuron-specific expression of a synaptotagmin gene in the sea urchin <i>Strongylocentrotus purpuratus</i>. <i>J. Comp. Neurol.</i> 496, 244-251
</Citation><ArticleIdList><ArticleId IdType="pubmed">16538680</ArticleId></ArticleIdList></Reference><Reference><Citation>
Chen H. B., Shen J., Ip Y. T., Xu L. (2006). Identification of phosphatases for Smad in the BMP/DPP pathway. <i>Gene Dev.</i> 20, 648-653
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC1413280</ArticleId><ArticleId IdType="pubmed">16510868</ArticleId></ArticleIdList></Reference><Reference><Citation>
De Robertis E. M., Kuroda H. (2004). Dorsal-ventral patterning and neural induction in <i>Xenopus</i> embryos. <i>Annu. Rev. Cell Dev. Biol.</i> 20, 285-308
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC2280069</ArticleId><ArticleId IdType="pubmed">15473842</ArticleId></ArticleIdList></Reference><Reference><Citation>
Deheuninck J., Luo K. (2009). Ski and SnoN, potent negative regulators of TGF-beta signaling. <i>Cell Res.</i> 19, 47-57
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC3103856</ArticleId><ArticleId IdType="pubmed">19114989</ArticleId></ArticleIdList></Reference><Reference><Citation>
Duboc V., Rottinger E., Besnardeau L., Lepage T. (2004). Nodal and BMP2/4 signaling organizes the oral-aboral axis of the sea urchin embryo. <i>Dev. Cell</i> 6, 397-410
</Citation><ArticleIdList><ArticleId IdType="pubmed">15030762</ArticleId></ArticleIdList></Reference><Reference><Citation>
Gardner T. S., Cantor C. R., Collins J. J. (2000). Construction of a genetic toggle switch in <i>Escherichia coli</i>. <i>Nature</i> 403, 339-342
</Citation><ArticleIdList><ArticleId IdType="pubmed">10659857</ArticleId></ArticleIdList></Reference><Reference><Citation>
Hirata T., Nakazawa M., Muraoka O., Nakayama R., Suda Y., Hibi M. (2006a). Zinc-finger genes Fez and Fez-like function in the establishment of diencephalon subdivisions. <i>Development</i> 133, 3993-4004
</Citation><ArticleIdList><ArticleId IdType="pubmed">16971467</ArticleId></ArticleIdList></Reference><Reference><Citation>
Hirata T., Nakazawa M., Yoshihara S., Miyachi H., Kitamura K., Yoshihara Y., Hibi M. (2006b). Zinc-finger gene Fez in the olfactory sensory neurons regulates development of the olfactory bulb non-cell-autonomously. <i>Development</i> 133, 1433-1443
</Citation><ArticleIdList><ArticleId IdType="pubmed">16540508</ArticleId></ArticleIdList></Reference><Reference><Citation>
Inman G. J., Nicol&#xe1;s F. J., Hill C. S. (2002). Nucleocytoplasmic shuttling of Smads 2, 3, and 4 permits sensing of TGF-&#x3b2; receptor activity. <i>Mol. Cell</i> 10, 283-294
</Citation><ArticleIdList><ArticleId IdType="pubmed">12191474</ArticleId></ArticleIdList></Reference><Reference><Citation>
Khokha M. K., Yeh J., Grammer T. C., Harland R. M. (2005). Depletion of three BMP antagonists from Spemann's organizer leads to a catastrophic loss of dorsal structures. <i>Dev. Cell</i> 8, 401-411
</Citation><ArticleIdList><ArticleId IdType="pubmed">15737935</ArticleId></ArticleIdList></Reference><Reference><Citation>
Kiecker C., Niehrs C. (2001). A morphogen gradient of Wnt/beta-catenin signaling regulates anteroposterior neural patterning in <i>Xenopus</i>. <i>Development</i> 128, 4189-4201
</Citation><ArticleIdList><ArticleId IdType="pubmed">11684656</ArticleId></ArticleIdList></Reference><Reference><Citation>
Lamb T. M., Knecht A. K., Smith W. C., Stachel S. E., Economides A. N., Stahl N., Yancopolous G. D., Harland R. M. (1993). Neural induction by the secreted polypeptide noggin. <i>Science</i> 262, 713-718
</Citation><ArticleIdList><ArticleId IdType="pubmed">8235591</ArticleId></ArticleIdList></Reference><Reference><Citation>
Lapraz F., Besnardeau L., Lepage T. (2009). Patterning of the dorsal-ventral axis in echinoderms: insights into the evolution of the BMP-chordin signaling network. <i>PLoS Biol.</i> 7, e1000248
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC2772021</ArticleId><ArticleId IdType="pubmed">19956794</ArticleId></ArticleIdList></Reference><Reference><Citation>
Lee H. X., Ambrosio A. L., Reversade B., De Robertis E. M. (2006). Embryonic dorsal-ventral signaling: secreted Frizzled-related proteins as inhibitors of tolloid proteinases. <i>Cell</i> 124, 147-159
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC2486255</ArticleId><ArticleId IdType="pubmed">16413488</ArticleId></ArticleIdList></Reference><Reference><Citation>
Logan C. Y., Miller J. R., Ferkowicz M. J., McClay D. R. (1999). Nuclear beta-catenin is required to specify vegetal cell fates in the sea urchin embryo. <i>Development</i> 126, 345-357
</Citation><ArticleIdList><ArticleId IdType="pubmed">9847248</ArticleId></ArticleIdList></Reference><Reference><Citation>
Materna S. C., Nam J., Davidson E. H. (2010). High accuracy, high-resolution prevalence measurement for the majority of locally expressed regulatory genes in early sea urchin development. <i>Gene Expr. Patterns</i> 10, 177-184
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC2902461</ArticleId><ArticleId IdType="pubmed">20398801</ArticleId></ArticleIdList></Reference><Reference><Citation>
Minokawa T., Rast J. P., Arenas-Mena C., Franco C. B., Davidson E. H. (2004). Expression patterns of four different regulatory genes that function during sea urchin development. <i>Gene Expr. Patterns</i> 4, 449-456
</Citation><ArticleIdList><ArticleId IdType="pubmed">15183312</ArticleId></ArticleIdList></Reference><Reference><Citation>
Nakajima Y., Kaneko H., Murray G., Burke R. D. (2004). Divergent patterns of neural development in larval echinoids and asteroids. <i>Evol. Dev.</i> 6, 95-104
</Citation><ArticleIdList><ArticleId IdType="pubmed">15009122</ArticleId></ArticleIdList></Reference><Reference><Citation>
Nitta K. R., Tanegashima K., Takahashi S., Asashima M. (2004). XSIP1 is essential for early neural gene expression and neural differentiation by suppression of BMP signaling. <i>Dev. Biol.</i> 275, 258-267
</Citation><ArticleIdList><ArticleId IdType="pubmed">15464588</ArticleId></ArticleIdList></Reference><Reference><Citation>
Piccolo S., Agius E., Lu B., Goodman S., Dale L., De Robertis E. M. (1997). Cleavage of Chordin by Xolloid metalloprotease suggests a role for proteolytic processing in the regulation of Spemann organizer activity. <i>Cell</i> 91, 407-416
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC3070600</ArticleId><ArticleId IdType="pubmed">9363949</ArticleId></ArticleIdList></Reference><Reference><Citation>
Plouhinec J. L., De Robertis E. M. (2009). Systems biology of the self-regulating morphogenetic gradient of the <i>Xenopus gastrula</i>. <i>Cold Spring Harb. Perspect. Biol.</i> 1, a001701
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC2742089</ArticleId><ArticleId IdType="pubmed">20066084</ArticleId></ArticleIdList></Reference><Reference><Citation>
Reversade B., Kuroda H., Lee H., Mays A., De Robertis E. M. (2005). Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in <i>Xenopus</i> embryos. <i>Development</i> 132, 3381-3392
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC2278118</ArticleId><ArticleId IdType="pubmed">15975940</ArticleId></ArticleIdList></Reference><Reference><Citation>
Sapkota G., Alarcon C., Spagnoli F. M., Brivanlou A. H., Massague J. (2007). Balancing BMP signaling through integrated inputs into the Smad1 linker. <i>Mol. Cell</i> 25, 441-454
</Citation><ArticleIdList><ArticleId IdType="pubmed">17289590</ArticleId></ArticleIdList></Reference><Reference><Citation>
Sasai Y., Lu B., Steinbeisser H., Geissert D., Gont L. K., De Robertis E. M. (1994). <i>Xenopus</i> chordin: a novel dorsalizing factor activated by organizer-specific homeobox genes. <i>Cell</i> 79, 779-790
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC3082463</ArticleId><ArticleId IdType="pubmed">8001117</ArticleId></ArticleIdList></Reference><Reference><Citation>
Saudemont A., Haillot E., Mekpoh F., Bessodes N., Quirin M., Lapraz F., Duboc V., Rottinger E., Range R., Oisel A., et al.  (2010). Ancestral regulatory circuits governing ectoderm patterning downstream of Nodal and BMP2/4 revealed by gene regulatory network analysis in an echinoderm. <i>PLoS Genet.</i> 6, e1001259
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC3009687</ArticleId><ArticleId IdType="pubmed">21203442</ArticleId></ArticleIdList></Reference><Reference><Citation>
Sea Urchin Genome Sequencing Consortium: Sodergren E., Weinstock G. M., Davidson E. H., Cameron R. A., Gibbs R. A., Angerer R. C., Angerer L. M., Arnone M. I., Burgess D. R., Burke R. D., et al.  (2006). The genome of the sea urchin <i>Strongylocentrotus purpuratus</i>. <i>Science</i> 314, 941-952
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC3159423</ArticleId><ArticleId IdType="pubmed">17095691</ArticleId></ArticleIdList></Reference><Reference><Citation>
Shen Z. J., Kim S. K., Jun D. Y., Park W., Kim Y. H., Malter J. S., Moon B. J. (2007). Antisense targeting of TGF-beta1 augments BMP-induced upregulation of osteopontin, type I collagen and Cbfa1 in human Saos-2 cells. <i>Exp. Cell Res.</i> 313, 1415-1425
</Citation><ArticleIdList><ArticleId IdType="pubmed">17359969</ArticleId></ArticleIdList></Reference><Reference><Citation>
Shimizu T., Hibi M. (2009). Formation and patterning of the forebrain and olfactory system by zinc-finger genes <i>Fezf1</i> and <i>Fezf2</i>. <i>Dev. Growth Differ.</i> 51, 221-231
</Citation><ArticleIdList><ArticleId IdType="pubmed">19222525</ArticleId></ArticleIdList></Reference><Reference><Citation>
Shimizu T., Nakazawa M., Kani S., Bae T.-K., Shimizu T., Kageyama R., Hibi M. (2010). Zinc finger genes <i>Fezf1</i> and <i>Fezf2</i> control neuronal differentiation by repressing <i>Hes5</i> expression in the forebrain. <i>Development</i> 137, 1875-1885
</Citation><ArticleIdList><ArticleId IdType="pubmed">20431123</ArticleId></ArticleIdList></Reference><Reference><Citation>
Spemann H., Mangold H. (1924). The induction of embryonic predispositions by implantation of organizers foreign to the species. <i>Arch. Mikrosk. Anat. Entwicklungsmech.</i> 100, 599-638
</Citation></Reference><Reference><Citation>
Tu Q., Brown C. T., Davidson E. H., Oliveri P. (2006). Sea urchin Forkhead gene family: phylogeny and embryonic expression. <i>Dev. Biol.</i> 300, 49-62
</Citation><ArticleIdList><ArticleId IdType="pubmed">17081512</ArticleId></ArticleIdList></Reference><Reference><Citation>
van Grunsven L. A., Michiels C., Van de Putte T., Nelles L., Wuytens G., Verschueren K., Huylebroeck D. (2003). Interaction between Smad-interacting protein-1 and the corepressor C-terminal binding protein is dispensable for transcriptional repression of E-cadherin. <i>J. Biol. Chem.</i> 278, 26135-26145
</Citation><ArticleIdList><ArticleId IdType="pubmed">12714599</ArticleId></ArticleIdList></Reference><Reference><Citation>
van Grunsven L. A., Taelman V., Michiels C., Verstappen G., Souopgui J., Nichane M., Moens E., Opdecamp K., Vanhomwegen J., Kricha S., et al.  (2007). XSip1 neuralizing activity involves the co-repressor CtBP and occurs through BMP dependent and independent mechanisms. <i>Dev. Biol.</i> 306, 34-49
</Citation><ArticleIdList><ArticleId IdType="pubmed">17442301</ArticleId></ArticleIdList></Reference><Reference><Citation>
Verschueren K., Remacle J. E., Collart C., Hraft H., Baker B. S., Tylzanowski P., Nelles L., Wuytens G., Su M.-T., Bodmer R., et al.  (1999). SIP1, a novel zinc finger/homeodomain repressor, interacts with Smad proteins and binds to 5&#x2032;-CACCT sequences in candidate target genes. <i>J. Biol. Chem.</i> 274, 20489-20498
</Citation><ArticleIdList><ArticleId IdType="pubmed">10400677</ArticleId></ArticleIdList></Reference><Reference><Citation>
Wei Z., Angerer R. C., Angerer L. M. (2006). A database of mRNA expression patterns for the sea urchin embryo. <i>Dev. Biol.</i> 300, 476-484
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC1762123</ArticleId><ArticleId IdType="pubmed">17007833</ArticleId></ArticleIdList></Reference><Reference><Citation>
Wei Z., Yaguchi J., Yaguchi S., Angerer R. C., Angerer L. M. (2009). The sea urchin animal pole domain is a Six3-dependent neurogenic patterning center. <i>Development</i> 136, 1179-1189
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC2685935</ArticleId><ArticleId IdType="pubmed">19270175</ArticleId></ArticleIdList></Reference><Reference><Citation>
Wei Z., Angerer R. C., Angerer L. M. (2011). Direct development of neurons within foregut endoderm of sea urchin embryos. <i>Proc. Natl. Acad. Sci. USA</i> 108, 9143-9147
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC3107264</ArticleId><ArticleId IdType="pubmed">21576476</ArticleId></ArticleIdList></Reference><Reference><Citation>
Weng M., Golden K. L., Lee C.-Y. (2010). dFezf/Earmuff maintains the restricted developmental potential of intermediate neural progenitors in <i>Drosophila</i>. <i>Dev. Cell</i> 18, 126-135
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC6699514</ArticleId><ArticleId IdType="pubmed">20152183</ArticleId></ArticleIdList></Reference><Reference><Citation>
Wikramanayake A. H., Huang L., Klein W. H. (1998). &#x3b2;-catenin is essential for patterning the maternally specified anima-vegetal axis in the sea urchin embryo. <i>Proc. Natl. Acad. Sci. USA</i> 95, 9343-9348
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC21340</ArticleId><ArticleId IdType="pubmed">9689082</ArticleId></ArticleIdList></Reference><Reference><Citation>
Yaguchi S., Katow H. (2003). Expression of tryptophan 5-hydroxylase gene during sea urchin neurogenesis and role of serotonergic nervous system in larval behavior. <i>J. Comp. Neurol.</i> 466, 219-229
</Citation><ArticleIdList><ArticleId IdType="pubmed">14528449</ArticleId></ArticleIdList></Reference><Reference><Citation>
Yaguchi S., Kanoh K., Amemiya S., Katow H. (2000). Initial analysis of immunochemical cell surface properties, location and formation of the serotonergic apical ganglion in sea urchin embryos. <i>Dev. Growth Differ.</i> 42, 479-488
</Citation><ArticleIdList><ArticleId IdType="pubmed">11041489</ArticleId></ArticleIdList></Reference><Reference><Citation>
Yaguchi S., Yaguchi J., Burke R. D. (2006). Specification of ectoderm restricts the size of the animal plate and patterns neurogenesis in sea urchin embryos. <i>Development</i> 133, 2337-2346
</Citation><ArticleIdList><ArticleId IdType="pubmed">16687447</ArticleId></ArticleIdList></Reference><Reference><Citation>
Yaguchi S., Yaguchi J., Burke R. D. (2007). Sp-Smad2/3 mediates patterning of neurogenic ectoderm by nodal in the sea urchin embryo. <i>Dev. Biol.</i> 302, 494-503
</Citation><ArticleIdList><ArticleId IdType="pubmed">17101124</ArticleId></ArticleIdList></Reference><Reference><Citation>
Yaguchi S., Yaguchi J., Angerer R. C., Angerer L. M. (2008). A Wnt-FoxQ2-nodal pathway links primary and secondary axis specification in sea urchin embryos. <i>Dev. Cell</i> 14, 97-107
</Citation><ArticleIdList><ArticleId IdType="pubmed">18194656</ArticleId></ArticleIdList></Reference><Reference><Citation>
Yaguchi S., Yaguchi J., Angerer R. C., Angerer L. M., Burke R. D. (2010a). TGFbeta signaling positions the ciliary band and patterns neurons in the sea urchin embryo. <i>Dev. Biol.</i> 347, 71-81
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC2950233</ArticleId><ArticleId IdType="pubmed">20709054</ArticleId></ArticleIdList></Reference><Reference><Citation>
Yaguchi S., Yaguchi J., Wei Z., Shiba K., Angerer L. M., Inaba K. (2010b). ankAT-1 is a novel gene mediating the apical tuft formation in the sea urchin embryo. <i>Dev. Biol.</i> 348, 67-75
</Citation><ArticleIdList><ArticleId IdType="pmc">PMC2976814</ArticleId><ArticleId IdType="pubmed">20875818</ArticleId></ArticleIdList></Reference></ReferenceList></PubmedData></PubmedArticle></PubmedArticleSet>