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<PubmedArticle><MedlineCitation Status="PubMed-not-MEDLINE" Owner="NLM"><PMID Version="1">32244588</PMID><DateRevised><Year>2020</Year><Month>09</Month><Day>28</Day></DateRevised><Article PubModel="Electronic"><Journal><ISSN IssnType="Electronic">2221-3759</ISSN><JournalIssue CitedMedium="Internet"><Volume>8</Volume><Issue>2</Issue><PubDate><Year>2020</Year><Month>Apr</Month><Day>01</Day></PubDate></JournalIssue><Title>Journal of developmental biology</Title><ISOAbbreviation>J Dev Biol</ISOAbbreviation></Journal><ArticleTitle><i>Gbx1</i> and <i>Gbx2</i> Are Essential for Normal Patterning and Development of Interneurons and Motor Neurons in the Embryonic Spinal Cord.</ArticleTitle><ELocationID EIdType="pii" ValidYN="Y">9</ELocationID><ELocationID EIdType="doi" ValidYN="Y">10.3390/jdb8020009</ELocationID><Abstract><AbstractText>The molecular mechanisms regulating neurogenesis involve the control of gene expression by transcription factors. <i>Gbx1</i> and <i>Gbx2</i>, two members of the Gbx family of homeodomain-containing transcription factors, are known for their essential roles in central nervous system development. The expression domains of mouse <i>Gbx1</i> and <i>Gbx2</i> include regions of the forebrain, anterior hindbrain, and spinal cord. In the spinal cord, <i>Gbx1</i> and <i>Gbx2</i> are expressed in PAX2<sup>+</sup> interneurons of the dorsal horn and ventral motor neuron progenitors. Based on their shared domains of expression and instances of overlap, we investigated the functional relationship between <i>Gbx</i> family members in the developing spinal cord using <i>Gbx1</i><sup>-/-</sup>, <i>Gbx2</i><sup>-/-</sup>, and <i>Gbx1</i><sup>-/-</sup>/<i>Gbx2</i><sup>-/-</sup> embryos. In situ hybridization analyses of embryonic spinal cords show upregulation of <i>Gbx2</i> expression in <i>Gbx1</i><sup>-/-</sup> embryos and upregulation of <i>Gbx1</i> expression in <i>Gbx2</i><sup>-/-</sup> embryos. Additionally, our data demonstrate that <i>Gbx</i> genes regulate development of a subset of PAX2<sup>+</sup> dorsal inhibitory interneurons. While we observe no difference in overall proliferative status of the developing ependymal layer, expansion of proliferative cells into the anatomically defined mantle zone occurs in <i>Gbx</i> mutants. Lastly, our data shows a marked increase in apoptotic cell death in the ventral spinal cord of <i>Gbx</i> mutants during mid-embryonic stages. While our studies reveal that both members of the <i>Gbx</i> gene family are involved in development of subsets of PAX2<sup>+</sup> dorsal interneurons and survival of ventral motor neurons, <i>Gbx1</i> and <i>Gbx2</i> are not sufficient to genetically compensate for the loss of one another. Thus, our studies provide novel insight to the relationship harbored between <i>Gbx1</i> and <i>Gbx2</i> in spinal cord development.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Buckley</LastName><ForeName>Desir&#xe8; M</ForeName><Initials>DM</Initials><Identifier Source="ORCID">0000-0003-4780-8173</Identifier><AffiliationInfo><Affiliation>Department of Molecular Biosciences, University of Texas at Austin, Austin, TX 78712, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Burroughs-Garcia</LastName><ForeName>Jessica</ForeName><Initials>J</Initials><AffiliationInfo><Affiliation>Section of Pediatric Hematology-Oncology, Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Kriks</LastName><ForeName>Sonja</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>Neurona Therapeutics, South San Francisco, CA 94080, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Lewandoski</LastName><ForeName>Mark</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Cancer and Developmental Biology Laboratory, National Cancer Institute, Frederick, MD 21702, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Waters</LastName><ForeName>Samuel T</ForeName><Initials>ST</Initials><AffiliationInfo><Affiliation>Division of Sciences and Mathematics, University of the District of Columbia, Washington, DC 20008, USA.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>NSF 1021288</GrantID><Agency>National Science Foundation</Agency><Country/></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2020</Year><Month>04</Month><Day>01</Day></ArticleDate></Article><MedlineJournalInfo><Country>Switzerland</Country><MedlineTA>J Dev Biol</MedlineTA><NlmUniqueID>101613409</NlmUniqueID><ISSNLinking>2221-3759</ISSNLinking></MedlineJournalInfo><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Gbx1</Keyword><Keyword MajorTopicYN="N">Gbx2</Keyword><Keyword MajorTopicYN="N">development</Keyword><Keyword MajorTopicYN="N">mouse</Keyword><Keyword MajorTopicYN="N">spinal cord</Keyword></KeywordList><CoiStatement>The authors declare no conflict of interest. The funders had no role in the design of the study, collection or interpretation of the data, or in preparation of the manuscript.</CoiStatement></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2019</Year><Month>12</Month><Day>17</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2020</Year><Month>3</Month><Day>1</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2020</Year><Month>3</Month><Day>26</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2020</Year><Month>4</Month><Day>5</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2020</Year><Month>4</Month><Day>5</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2020</Year><Month>4</Month><Day>5</Day><Hour>6</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="pmc-release"><Year>2020</Year><Month>4</Month><Day>1</Day></PubMedPubDate></History><PublicationStatus>epublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">32244588</ArticleId><ArticleId IdType="pmc">PMC7345146</ArticleId><ArticleId IdType="doi">10.3390/jdb8020009</ArticleId><ArticleId IdType="pii">jdb8020009</ArticleId></ArticleIdList><ReferenceList><Reference><Citation>Jessell T.M. Neuronal specification in the spinal cord: Inductive signals and transcriptional codes. Nat. Rev. Genet. 2000;1:20&#x2013;29. doi: 10.1038/35049541.</Citation><ArticleIdList><ArticleId IdType="doi">10.1038/35049541</ArticleId><ArticleId IdType="pubmed">11262869</ArticleId></ArticleIdList></Reference><Reference><Citation>Goulding M., Lanuza G., Sapir T., Narayan S. The formation of sensorimotor circuits. Curr. Opin. Neurobiol. 2002;12:508&#x2013;515. doi: 10.1016/S0959-4388(02)00371-9.</Citation><ArticleIdList><ArticleId IdType="doi">10.1016/S0959-4388(02)00371-9</ArticleId><ArticleId IdType="pubmed">12367629</ArticleId></ArticleIdList></Reference><Reference><Citation>Briscoe J., Pierani A., Jessell T.M., Ericson J. A homeodomain protein code specifies progenitor cell identity and neuronal fate in the ventral neural tube. Cell. 2000;101:435&#x2013;445. doi: 10.1016/S0092-8674(00)80853-3.</Citation><ArticleIdList><ArticleId IdType="doi">10.1016/S0092-8674(00)80853-3</ArticleId><ArticleId IdType="pubmed">10830170</ArticleId></ArticleIdList></Reference><Reference><Citation>Caspary T., Anderson K.V. Patterning cell types in the dorsal spinal cord: What the mouse mutants say. Nat. Rev. Neurosci. 2003;4:289&#x2013;297. doi: 10.1038/nrn1073.</Citation><ArticleIdList><ArticleId IdType="doi">10.1038/nrn1073</ArticleId><ArticleId IdType="pubmed">12671645</ArticleId></ArticleIdList></Reference><Reference><Citation>Gross M.K., Dottori M., Goulding M. Lbx1 specifies somatosensory association interneurons in the dorsal spinal cord. Neuron. 2002;34:535&#x2013;549. doi: 10.1016/S0896-6273(02)00690-6.</Citation><ArticleIdList><ArticleId IdType="doi">10.1016/S0896-6273(02)00690-6</ArticleId><ArticleId IdType="pubmed">12062038</ArticleId></ArticleIdList></Reference><Reference><Citation>M&#xfc;ller T., Brohmann H., Pierani A., Heppenstall P.A., Lewin G.R., Jessell T.M., Birchmeier C. The homeodomain factor lbx1 distinguishes two major programs of neuronal differentiation in the dorsal spinal cord. Neuron. 2002;34:551&#x2013;562. doi: 10.1016/S0896-6273(02)00689-X.</Citation><ArticleIdList><ArticleId IdType="doi">10.1016/S0896-6273(02)00689-X</ArticleId><ArticleId IdType="pubmed">12062039</ArticleId></ArticleIdList></Reference><Reference><Citation>Julius D., Basbaum A.I. Molecular mechanisms of nociception. Nature. 2001;413:203&#x2013;210. doi: 10.1038/35093019.</Citation><ArticleIdList><ArticleId IdType="doi">10.1038/35093019</ArticleId><ArticleId IdType="pubmed">11557989</ArticleId></ArticleIdList></Reference><Reference><Citation>Gillespie P.G., Walker R.G. Molecular basis of mechanosensory transduction. Nature. 2001;413:194&#x2013;202. doi: 10.1038/35093011.</Citation><ArticleIdList><ArticleId IdType="doi">10.1038/35093011</ArticleId><ArticleId IdType="pubmed">11557988</ArticleId></ArticleIdList></Reference><Reference><Citation>Helms A.W., Johnson J.E. Specification of dorsal spinal cord interneurons. Curr. Opin. Neurobiol. 2003;13:42&#x2013;49. doi: 10.1016/S0959-4388(03)00010-2.</Citation><ArticleIdList><ArticleId IdType="doi">10.1016/S0959-4388(03)00010-2</ArticleId><ArticleId IdType="pubmed">12593981</ArticleId></ArticleIdList></Reference><Reference><Citation>Pillai A., Mansouri A., Behringer R., Westphal H., Goulding M. Lhx1 and Lhx5 maintain the inhibitory-neurotransmitter status of interneurons in the dorsal spinal cord. Development. 2007;134:357&#x2013;366. doi: 10.1242/dev.02717.</Citation><ArticleIdList><ArticleId IdType="doi">10.1242/dev.02717</ArticleId><ArticleId IdType="pubmed">17166926</ArticleId></ArticleIdList></Reference><Reference><Citation>Cheng L., Arata A., Mizuguchi R., Qian Y., Karunaratne A., Gray P.A., Arata S., Shirasawa S., Bouchard M., Luo P., et al. Tlx3 and Tlx1 are post-mitotic selector genes determining glutamatergic over GABAergic cell fates. Nat. Neurosci. 2004;7:510&#x2013;517. doi: 10.1038/nn1221.</Citation><ArticleIdList><ArticleId IdType="doi">10.1038/nn1221</ArticleId><ArticleId IdType="pubmed">15064766</ArticleId></ArticleIdList></Reference><Reference><Citation>Mizuguchi R., Kriks S., Cordes R., Gossler A., Ma Q., Goulding M. Ascl1 and Gsh1/2 control inhibitory and excitatory cell fate in spinal sensory interneurons. Nat. Neurosci. 2006;9:770&#x2013;778. doi: 10.1038/nn1706.</Citation><ArticleIdList><ArticleId IdType="doi">10.1038/nn1706</ArticleId><ArticleId IdType="pubmed">16715081</ArticleId></ArticleIdList></Reference><Reference><Citation>Glasgow S.M., Henke R.M., MacDonald R.J., Wright C.V., Johnson J.E. Ptf1a determines GABAergic over glutamatergic neuronal cell fate in the spinal cord dorsal horn. Development. 2005;132:5461&#x2013;5469. doi: 10.1242/dev.02167.</Citation><ArticleIdList><ArticleId IdType="doi">10.1242/dev.02167</ArticleId><ArticleId IdType="pubmed">16291784</ArticleId></ArticleIdList></Reference><Reference><Citation>Wildner H., Gupta R.D., Br&#xf6;hl D., Heppenstall P.A., Zeilhofer H.U., Birchmeier C. Genome-wide expression analysis of Ptf1a- and Ascl1-deficient mice reveals new markers for distinct dorsal horn interneuron populations contributing to nociceptive reflex plasticity. J. Neurosci. 2013;33:7299&#x2013;7307. doi: 10.1523/JNEUROSCI.0491-13.2013.</Citation><ArticleIdList><ArticleId IdType="doi">10.1523/JNEUROSCI.0491-13.2013</ArticleId><ArticleId IdType="pmc">PMC3684736</ArticleId><ArticleId IdType="pubmed">23616538</ArticleId></ArticleIdList></Reference><Reference><Citation>Ulloa F., Briscoe J. Morphogens and the control of cell proliferation and patterning in the spinal cord. Cell Cycle. 2007;6:2640&#x2013;2649. doi: 10.4161/cc.6.21.4822.</Citation><ArticleIdList><ArticleId IdType="doi">10.4161/cc.6.21.4822</ArticleId><ArticleId IdType="pubmed">17912034</ArticleId></ArticleIdList></Reference><Reference><Citation>Goulding M. Circuits controlling vertebrate locomotion: Moving in a new direction. Nat. Rev. Neurosci. 2009;10:507&#x2013;518. doi: 10.1038/nrn2608.</Citation><ArticleIdList><ArticleId IdType="doi">10.1038/nrn2608</ArticleId><ArticleId IdType="pmc">PMC2847453</ArticleId><ArticleId IdType="pubmed">19543221</ArticleId></ArticleIdList></Reference><Reference><Citation>Arber S. Motor circuits in action: Specification, connectivity, and function. Neuron. 2012;74:975&#x2013;989. doi: 10.1016/j.neuron.2012.05.011.</Citation><ArticleIdList><ArticleId IdType="doi">10.1016/j.neuron.2012.05.011</ArticleId><ArticleId IdType="pubmed">22726829</ArticleId></ArticleIdList></Reference><Reference><Citation>Ericson J., Rashbass P., Schedl A., Brenner-Morton S.K.A.W.A.K.A.M.I., Kawakami A., Van Heyningen V., Jessell T.M., Briscoe J. Pax6 controls progenitor cell identity and neuronal fate in response to graded Shh signaling. Cell. 1997;90:169&#x2013;180. doi: 10.1016/S0092-8674(00)80323-2.</Citation><ArticleIdList><ArticleId IdType="doi">10.1016/S0092-8674(00)80323-2</ArticleId><ArticleId IdType="pubmed">9230312</ArticleId></ArticleIdList></Reference><Reference><Citation>Waters S.T., Lewandoski M. A threshold requirement for Gbx2 levels in hindbrain development. Development. 2006;133:1991&#x2013;2000. doi: 10.1242/dev.02364.</Citation><ArticleIdList><ArticleId IdType="doi">10.1242/dev.02364</ArticleId><ArticleId IdType="pubmed">16651541</ArticleId></ArticleIdList></Reference><Reference><Citation>Wassarman K.M., Lewandoski M., Campbell K., Joyner A.L., Rubenstein J.L., Martinez S., Martin G.R. Specification of the anterior hindbrain and establishment of a normal mid/hindbrain organizer is dependent on Gbx2 gene function. Development. 1997;124:2923&#x2013;2934.</Citation><ArticleIdList><ArticleId IdType="pubmed">9247335</ArticleId></ArticleIdList></Reference><Reference><Citation>Luu B., Ellisor D., Zervas M. The lineage contribution and role of Gbx2 in spinal cord development. PLoS ONE. 2011;6:e20940. doi: 10.1371/journal.pone.0020940.</Citation><ArticleIdList><ArticleId IdType="doi">10.1371/journal.pone.0020940</ArticleId><ArticleId IdType="pmc">PMC3116860</ArticleId><ArticleId IdType="pubmed">21698205</ArticleId></ArticleIdList></Reference><Reference><Citation>Liu A., Joyner A.L. EN and GBX2 play essential roles downstream of FGF8 in patterning the mouse mid/hindbrain region. Development. 2001;128:181&#x2013;191.</Citation><ArticleIdList><ArticleId IdType="pubmed">11124114</ArticleId></ArticleIdList></Reference><Reference><Citation>Li J.Y., Lao Z., Joyner A.L. Changing requirements for Gbx2 in development of the cerebellum and maintenance of the mid/hindbrain organizer. Neuron. 2002;36:31&#x2013;43. doi: 10.1016/S0896-6273(02)00935-2.</Citation><ArticleIdList><ArticleId IdType="doi">10.1016/S0896-6273(02)00935-2</ArticleId><ArticleId IdType="pubmed">12367504</ArticleId></ArticleIdList></Reference><Reference><Citation>Burroughs-Garcia J., Sittaramane V., Chandrasekhar A., Waters S.T. Evolutionarily conserved function of Gbx2 in anterior hindbrain development. Dev. Dyn. 2011;240:828&#x2013;838. doi: 10.1002/dvdy.22589.</Citation><ArticleIdList><ArticleId IdType="doi">10.1002/dvdy.22589</ArticleId><ArticleId IdType="pubmed">21360792</ArticleId></ArticleIdList></Reference><Reference><Citation>Buckley D.M., Burroughs-Garcia J., Lewandoski M., Waters S.T. Characterization of the Gbx1&#x2212;/&#x2212; mouse mutant: A requirement for Gbx1 in normal locomotion and sensorimotor circuit development. PLoS ONE. 2013;8:e56214. doi: 10.1371/journal.pone.0056214.</Citation><ArticleIdList><ArticleId IdType="doi">10.1371/journal.pone.0056214</ArticleId><ArticleId IdType="pmc">PMC3572027</ArticleId><ArticleId IdType="pubmed">23418536</ArticleId></ArticleIdList></Reference><Reference><Citation>Del Barrio M.G., Bourane S., Grossmann K., Sch&#xfc;le R., Britsch S., O&#x2019;Leary D.D., Goulding M. A transcription factor code defines nine sensory interneuron subtypes in the mechanosensory area of the spinal cord. PLoS ONE. 2013;8:e77928. doi: 10.1371/journal.pone.0077928.</Citation><ArticleIdList><ArticleId IdType="doi">10.1371/journal.pone.0077928</ArticleId><ArticleId IdType="pmc">PMC3817166</ArticleId><ArticleId IdType="pubmed">24223744</ArticleId></ArticleIdList></Reference><Reference><Citation>Su C.Y., Kemp H.A., Moens C.B. Cerebellar development in the absence of Gbx function in zebrafish. Dev. Biol. 2014;386:181&#x2013;190. doi: 10.1016/j.ydbio.2013.10.026.</Citation><ArticleIdList><ArticleId IdType="doi">10.1016/j.ydbio.2013.10.026</ArticleId><ArticleId IdType="pmc">PMC3935510</ArticleId><ArticleId IdType="pubmed">24183937</ArticleId></ArticleIdList></Reference><Reference><Citation>Meziane H., Fraulob V., Riet F., Krezel W., Selloum M., Geffarth M., Acampora D., H&#xe9;rault Y., Simeone A., Brand M., et al. The homeodomain factor Gbx1 is required for locomotion and cell specification in the dorsal spinal cord. PeerJ. 2013;1:e142. doi: 10.7717/peerj.142.</Citation><ArticleIdList><ArticleId IdType="doi">10.7717/peerj.142</ArticleId><ArticleId IdType="pmc">PMC3757465</ArticleId><ArticleId IdType="pubmed">24010020</ArticleId></ArticleIdList></Reference><Reference><Citation>Waters S.T., Wilson C.P., Lewandoski M. Cloning and embryonic expression analysis of the mouse Gbx1 gene. Gene Expr. Patterns. 2003;3:313&#x2013;317. doi: 10.1016/S1567-133X(03)00041-3.</Citation><ArticleIdList><ArticleId IdType="doi">10.1016/S1567-133X(03)00041-3</ArticleId><ArticleId IdType="pubmed">12799077</ArticleId></ArticleIdList></Reference><Reference><Citation>John A., Wildner H., Britsch S. The homeodomain transcription factor Gbx1 identifies a subpopulation of late-born GABAergic interneurons in the developing dorsal spinal cord. Dev. Dyn. 2005;234:767&#x2013;771. doi: 10.1002/dvdy.20568.</Citation><ArticleIdList><ArticleId IdType="doi">10.1002/dvdy.20568</ArticleId><ArticleId IdType="pubmed">16193514</ArticleId></ArticleIdList></Reference><Reference><Citation>Tourtellotte W.G., Nagarajan R., Bartke A., Milbrandt J. Functional compensation by Egr4 in Egr1-dependent luteinizing hormone regulation and Leydig cell steroidogenesis. Mol. Cell Biol. 2000;20:5261&#x2013;5268. doi: 10.1128/MCB.20.14.5261-5268.2000.</Citation><ArticleIdList><ArticleId IdType="doi">10.1128/MCB.20.14.5261-5268.2000</ArticleId><ArticleId IdType="pmc">PMC85975</ArticleId><ArticleId IdType="pubmed">10866682</ArticleId></ArticleIdList></Reference><Reference><Citation>Relaix F., Rocancourt D., Mansouri A., Buckingham M. Divergent functions of murine Pax3 and Pax7 in limb muscle development. Genes Dev. 2004;18:1088&#x2013;1105. doi: 10.1101/gad.301004.</Citation><ArticleIdList><ArticleId IdType="doi">10.1101/gad.301004</ArticleId><ArticleId IdType="pmc">PMC406297</ArticleId><ArticleId IdType="pubmed">15132998</ArticleId></ArticleIdList></Reference><Reference><Citation>Hanks M., Wurst W., Anson-Cartwright L., Auerbach A.B., Joyner A.L. Rescue of the En-1 mutant phenotype by replacement of En-1 with En-2. Science. 1995;269:679&#x2013;682. doi: 10.1126/science.7624797.</Citation><ArticleIdList><ArticleId IdType="doi">10.1126/science.7624797</ArticleId><ArticleId IdType="pubmed">7624797</ArticleId></ArticleIdList></Reference><Reference><Citation>Urb&#xe1;nek P., Fetka I., Meisler M.H., Busslinger M. Cooperation of Pax2 and Pax5 in midbrain and cerebellum development. Proc. Natl. Acad. Sci. USA. 1997;94:5703&#x2013;5708. doi: 10.1073/pnas.94.11.5703.</Citation><ArticleIdList><ArticleId IdType="doi">10.1073/pnas.94.11.5703</ArticleId><ArticleId IdType="pmc">PMC20842</ArticleId><ArticleId IdType="pubmed">9159136</ArticleId></ArticleIdList></Reference><Reference><Citation>Lin Z., Cantos R., Patente M., Wu D.K. Gbx2 is required for the morphogenesis of the mouse inner ear: A downstream candidate of hindbrain signaling. Development. 2005;132:2309&#x2013;2318. doi: 10.1242/dev.01804.</Citation><ArticleIdList><ArticleId IdType="doi">10.1242/dev.01804</ArticleId><ArticleId IdType="pubmed">15829521</ArticleId></ArticleIdList></Reference><Reference><Citation>Byrd N.A., Meyers E.N. Loss of Gbx2 results in neural crest cell patterning and pharyngeal arch artery defects in the mouse embryo. Dev. Biol. 2005;284:233&#x2013;245. doi: 10.1016/j.ydbio.2005.05.023.</Citation><ArticleIdList><ArticleId IdType="doi">10.1016/j.ydbio.2005.05.023</ArticleId><ArticleId IdType="pubmed">15996652</ArticleId></ArticleIdList></Reference><Reference><Citation>Villalon E., Schulz D.J., Waters S.T. Real-time PCR quantification of gene expression in embryonic mouse tissue. Methods Mol. Biol. 2014;1092:81&#x2013;94.</Citation><ArticleIdList><ArticleId IdType="pubmed">24318815</ArticleId></ArticleIdList></Reference><Reference><Citation>Smart I.H. Proliferative characteristics of the ependymal layer during the early development of the mouse diencephalon, as revealed by recording the number, location, and plane of cleavage of mitotic figures. Pt 1J. Anat. 1972;113:109&#x2013;129.</Citation><ArticleIdList><ArticleId IdType="pmc">PMC1271371</ArticleId><ArticleId IdType="pubmed">4648478</ArticleId></ArticleIdList></Reference><Reference><Citation>Alnemri E.S., Livingston D.J., Nicholson D.W., Salvesen G., Thornberry N.A., Wong W.W., Yuan J. Human ICE/CED-3 protease nomenclature. Cell. 1996;87:171. doi: 10.1016/S0092-8674(00)81334-3.</Citation><ArticleIdList><ArticleId IdType="doi">10.1016/S0092-8674(00)81334-3</ArticleId><ArticleId IdType="pubmed">8861900</ArticleId></ArticleIdList></Reference><Reference><Citation>Wolpert L. Positional information and the spatial pattern of cellular differentiation. J. Theor. Biol. 1969;25:1&#x2013;47. doi: 10.1016/S0022-5193(69)80016-0.</Citation><ArticleIdList><ArticleId IdType="doi">10.1016/S0022-5193(69)80016-0</ArticleId><ArticleId IdType="pubmed">4390734</ArticleId></ArticleIdList></Reference><Reference><Citation>Liu F., Morrison A.H., Gregor T. Dynamic interpretation of maternal inputs by the Drosophila segmentation gene network. Proc. Natl. Acad. Sci. USA. 2013;110:6724&#x2013;6729. doi: 10.1073/pnas.1220912110.</Citation><ArticleIdList><ArticleId IdType="doi">10.1073/pnas.1220912110</ArticleId><ArticleId IdType="pmc">PMC3637740</ArticleId><ArticleId IdType="pubmed">23580621</ArticleId></ArticleIdList></Reference><Reference><Citation>Prasad T., Wang X., Gray P.A., Weiner J.A. A differential developmental pattern of spinal interneuron apoptosis during synaptogenesis: Insights from genetic analyses of the protocadherin-gamma gene cluster. Development. 2008;135:4153&#x2013;4164. doi: 10.1242/dev.026807.</Citation><ArticleIdList><ArticleId IdType="doi">10.1242/dev.026807</ArticleId><ArticleId IdType="pmc">PMC2755264</ArticleId><ArticleId IdType="pubmed">19029045</ArticleId></ArticleIdList></Reference><Reference><Citation>Lowrie M.B., Lawson S.J. Cell death of spinal interneurones. Prog. Neurobiol. 2000;61:543&#x2013;555. doi: 10.1016/S0301-0082(99)00065-9.</Citation><ArticleIdList><ArticleId IdType="doi">10.1016/S0301-0082(99)00065-9</ArticleId><ArticleId IdType="pubmed">10775796</ArticleId></ArticleIdList></Reference><Reference><Citation>Oppenheim R.W. Cell death during development of the nervous system. Annu. Rev. Neurosci. 1991;14:453&#x2013;501. doi: 10.1146/annurev.ne.14.030191.002321.</Citation><ArticleIdList><ArticleId IdType="doi">10.1146/annurev.ne.14.030191.002321</ArticleId><ArticleId IdType="pubmed">2031577</ArticleId></ArticleIdList></Reference><Reference><Citation>Mennerick S., Zorumski C.F. Neural activity and survival in the developing nervous system. Mol. Neurobiol. 2000;22:41&#x2013;54.</Citation><ArticleIdList><ArticleId IdType="pubmed">11414280</ArticleId></ArticleIdList></Reference><Reference><Citation>Rhinn M., Lun K., Amores A., Yan Y.L., Postlethwait J.H., Brand M. Cloning, expression and relationship of zebrafish gbx1 and gbx2 genes to Fgf signaling. Mech. Dev. 2003;120:919&#x2013;936. doi: 10.1016/S0925-4773(03)00135-7.</Citation><ArticleIdList><ArticleId IdType="doi">10.1016/S0925-4773(03)00135-7</ArticleId><ArticleId IdType="pubmed">12963112</ArticleId></ArticleIdList></Reference><Reference><Citation>Kikuta H., Kanai M., Ito Y., Yamasu K. gbx2 Homeobox gene is required for the maintenance of the isthmic region in the zebrafish embryonic brain. Dev. Dyn. 2003;228:433&#x2013;450. doi: 10.1002/dvdy.10409.</Citation><ArticleIdList><ArticleId IdType="doi">10.1002/dvdy.10409</ArticleId><ArticleId IdType="pubmed">14579382</ArticleId></ArticleIdList></Reference><Reference><Citation>Sugiyama S., Di Nardo A.A., Aizawa S., Matsuo I., Volovitch M., Prochiantz A., Hensch T.K. Experience-dependent transfer of Otx2 homeoprotein into the visual cortex activates postnatal plasticity. Cell. 2008;134:508&#x2013;520. doi: 10.1016/j.cell.2008.05.054.</Citation><ArticleIdList><ArticleId IdType="doi">10.1016/j.cell.2008.05.054</ArticleId><ArticleId IdType="pubmed">18692473</ArticleId></ArticleIdList></Reference><Reference><Citation>Lesaffre B., Joliot A., Prochiantz A., Volovitch M. Direct non-cell autonomous Pax6 activity regulates eye development in the zebrafish. Neural Dev. 2007;2:2. doi: 10.1186/1749-8104-2-2.</Citation><ArticleIdList><ArticleId IdType="doi">10.1186/1749-8104-2-2</ArticleId><ArticleId IdType="pmc">PMC1797170</ArticleId><ArticleId IdType="pubmed">17229313</ArticleId></ArticleIdList></Reference><Reference><Citation>Brunet I., Weinl C., Piper M., Trembleau A., Volovitch M., Harris W., Prochiantz A., Holt C. The transcription factor Engrailed-2 guides retinal axons. Nature. 2005;438:94&#x2013;98. doi: 10.1038/nature04110.</Citation><ArticleIdList><ArticleId IdType="doi">10.1038/nature04110</ArticleId><ArticleId IdType="pmc">PMC3785142</ArticleId><ArticleId IdType="pubmed">16267555</ArticleId></ArticleIdList></Reference><Reference><Citation>Han D.Y., Kobayashi M., Nakano M., Atobe Y., Kadota T., Funakoshi K. Differential Islet-1 expression among lumbosacral spinal motor neurons in prenatal mouse. Brain Res. 2009;1265:30&#x2013;36. doi: 10.1016/j.brainres.2009.02.020.</Citation><ArticleIdList><ArticleId IdType="doi">10.1016/j.brainres.2009.02.020</ArticleId><ArticleId IdType="pubmed">19236857</ArticleId></ArticleIdList></Reference></ReferenceList></PubmedData></PubmedArticle></PubmedArticleSet>