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      An Update on the Molecular Mechanism of the Vertebrate Isthmic Organizer Development in the Context of the Neuromeric Model

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          Abstract

          A crucial event during the development of the central nervous system (CNS) is the early subdivision of the neural tube along its anterior-to-posterior axis to form neuromeres, morphogenetic units separated by transversal constrictions and programed for particular genetic cascades. The narrower portions observed in the developing neural tube are responsible for relevant cellular and molecular processes, such as clonal restrictions, expression of specific regulatory genes, and differential fate specification, as well as inductive activities. In this developmental context, the gradual formation of the midbrain-hindbrain (MH) constriction has been an excellent model to study the specification of two major subdivisions of the CNS containing the mesencephalic and isthmo-cerebellar primordia. This MH boundary is coincident with the common Otx2-(midbrain)/ Gbx2-(hindbrain) expressing border. The early interactions between these two pre-specified areas confer positional identities and induce the generation of specific diffusible morphogenes at this interface, in particular FGF8 and WNT1. These signaling pathways are responsible for the gradual histogenetic specifications and cellular identity acquisitions with in the MH domain. This review is focused on the cellular and molecular mechanisms involved in the specification of the midbrain/hindbrain territory and the formation of the isthmic organizer. Emphasis will be placed on the chick/quail chimeric experiments leading to the acquisition of the first fate mapping and experimental data to, in this way, better understand pioneering morphological studies and innovative gain/loss-of-function analysis.

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          Forebrain gene expression domains and the evolving prosomeric model.

          The prosomeric model attributes morphological meaning to gene expression patterns and other data in the forebrain. It divides this territory into the same transverse segments (prosomeres) and longitudinal zones in all vertebrates. The axis and longitudinal zones of this model are widely accepted but controversy subsists about the number of prosomeres and their nature as segments. We describe difficulties encountered in establishing continuity between prosomeric limits postulated in the hypothalamus and intra-telencephalic limits. Such difficulties throw doubt on the intersegmental nature of these limits. We sketch a simplified model, in which the secondary prosencephalon (telencephalon plus hypothalamus) is a complex protosegment not subdivided into prosomeres, which exhibits patterning singularities. By contrast, we continue to postulate that prosomeres p1-p3 (i.e. the pretectum, thalamus and prethalamus) are the caudal forebrain.
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            The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain.

            The Wnt-1 (int-1) proto-oncogene, which encodes a putative signaling molecule, is expressed exclusively in the developing central nervous system and adult testes. To examine the role of Wnt-1, we generated six independent embryonic stem cell lines in which insertion of a neoR gene by homologous recombination inactivated a Wnt-1 allele. Germline chimeras were generated from two lines, and progeny from matings between heterozygous parents were examined. In all day 9.5 fetuses homozygous for mutated Wnt-1 alleles, most of the midbrain and some rostral metencephalon were absent. The remainder of the neural tube and all other tissues were normal. In late-gestation homozygotes, there was virtually no midbrain and no cerebellum, while the rest of the fetus was normal. Homozygotes are born, but die within 24 hr. Thus the normal role of Wnt-1 is in determination or subsequent development of a specific region of the central nervous system.
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              An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombination.

              We describe a strategy for generating an allelic series of mutations at a given locus that requires the production of only one targetted mouse line. The 'allelogenic' mouse line we produced carries a hypomorphic allele of Fgf8, which can be converted to a null allele by mating to cre transgenic animals. The hypomorphic allele can also be reverted to wild-type by mating the allelogenic mice to flp transgenic animals, thereby generating a mouse line suitable for Cre-induced tissue-specific knockout experiments. Analysis of embryos carrying different combinations of these alleles revealed requirements for Fgf8 gene function during gastrulation, as well as cardiac, craniofacial, forebrain, midbrain and cerebellar development.
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                Author and article information

                Contributors
                Journal
                Front Neuroanat
                Front Neuroanat
                Front. Neuroanat
                Frontiers in Neuroanatomy
                Frontiers Media S.A.
                1662-5129
                24 March 2022
                2022
                : 16
                : 826976
                Affiliations
                [1] 1Departamento de Biología Celular, Facultad de Ciencias, Universidad de Extremadura , Badajoz, Spain
                [2] 2Instituto de Neurociencias de Alicante, Universidad Miguel Hernández-CSIC , Alicante, Spain
                Author notes

                Edited by: Fernando de Castro, Cajal Institute (CSIC), Spain

                Reviewed by: Kyo Yamasu, Saitama University, Japan; James Y. H. Li, University of Connecticut Health Center, United States

                *Correspondence: Matías Hidalgo-Sánchez mhidalgo@ 123456unex.es Diego Echevarria diegoaza@ 123456umh.es
                Article
                10.3389/fnana.2022.826976
                8987131
                35401126
                8acc6220-440f-43e6-a59a-801a245e5396
                Copyright © 2022 Hidalgo-Sánchez, Andreu-Cervera, Villa-Carballar and Echevarria.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 01 December 2021
                : 28 February 2022
                Page count
                Figures: 10, Tables: 0, Equations: 0, References: 262, Pages: 25, Words: 22292
                Funding
                Funded by: Junta de Extremadura, doi 10.13039/501100014181;
                Funded by: Generalitat Valenciana, doi 10.13039/501100003359;
                Categories
                Neuroscience
                Review

                Neurosciences
                midbrain,hindbrain,otx2,gbx2,engrailed,pax,fgf8,wnt1
                Neurosciences
                midbrain, hindbrain, otx2, gbx2, engrailed, pax, fgf8, wnt1

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