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dc.contributor.author한평림-
dc.date.accessioned2018-05-18T08:15:16Z-
dc.date.available2018-05-18T08:15:16Z-
dc.date.issued2005-
dc.identifier.issn0022-3034-
dc.identifier.otherOAK-2591-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/243204-
dc.description.abstractDorsoventral patterning of the Drosophila ventral neuroectoderm is established by the expression of three evolutionarily conserved homeodomain genes: ventral nervous system defective (vnd), intermediate neuroblasts defective (ind), and muscle segment homeobox (msh) in the medial, intermediate, and lateral columns of the ventral neuroectoderm, respectively. It was not clear whether extrinsic factor(s) from the CNS midline cells influence the initial dorsoventral patterning by controlling the expression of the dorsoventral patterning genes. We show here that the CNS midline cells, specified by single-minded (sim), are essential for maintaining expression of the dorsoventral patterning genes. Ectopic expression of sim in the ventral neuroectoderm during the blastoderm stage repressed expression of the three homeodomain genes in the ventral neuroectoderm. This indicates that the identity of the CNS midline cells is established by a series of repressions of the three homeodomain genes in the ventral neuroectoderm. Ectopic expression of sim in the ventral neuroectoderm during initial neurogenesis induced ectopic ind expression in the medial column in addition to that in the intermediate column via EGFR signaling between the ventral neuroectoderm and midline cells. In contrast, it repressed the expression of vnd and msh in the medial and lateral columns, respectively. Our findings demonstrate that the CNS midline cells provide extrinsic positional information via EGFR signaling that maintains the initial subdivision of the ventral neuroectoderm into three dorsoventral columns during initial neurogenesis. © 2004 Wiley Periodicals, Inc.-
dc.languageEnglish-
dc.titleCNS midline cells contribute to maintenance of the initial dorsoventral patterning of the Drosophila ventral neuroectoderm-
dc.typeArticle-
dc.relation.issue4-
dc.relation.volume62-
dc.relation.indexSCOPUS-
dc.relation.startpage397-
dc.relation.lastpage405-
dc.relation.journaltitleJournal of Neurobiology-
dc.identifier.doi10.1002/neu.20104-
dc.identifier.wosidWOS:000227077600001-
dc.identifier.scopusid2-s2.0-13844299856-
dc.author.googleIn O.K.-
dc.author.googleIn C.K.-
dc.author.googleKim S.-
dc.author.googleYeon K.K.-
dc.author.googleHan P.-L.-
dc.author.googleJeon S.-H.-
dc.author.googleSang H.K.-
dc.contributor.scopusid한평림(7201947605)-
dc.date.modifydate20230901081001-
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