Dorsal and lateral fates in the mouse neural tube require the cell-autonomous activity of the open brain gene

Citation
Jt. Eggenschwiler et Kv. Anderson, Dorsal and lateral fates in the mouse neural tube require the cell-autonomous activity of the open brain gene, DEVELOP BIO, 227(2), 2000, pp. 648-660
Citations number
43
Categorie Soggetti
Cell & Developmental Biology
Journal title
DEVELOPMENTAL BIOLOGY
ISSN journal
00121606 → ACNP
Volume
227
Issue
2
Year of publication
2000
Pages
648 - 660
Database
ISI
SICI code
0012-1606(20001115)227:2<648:DALFIT>2.0.ZU;2-9
Abstract
The processes that specify early regional identity in dorsal and lateral re gions of the mammalian neural tube are not well understood. The mouse open brain (opb) gene plays an essential role in dorsal neural patterning: in th e caudal spinal cord of opb mutants, dorsal cell types are absent and marke rs of ventral fates, including Shh, expand into dorsal regions. Analysis of the opb mutant phenotype and of opb/opb <-> wild-type chimeric embryos rev eals that early in neural development, the wild-type opb gene (opb(+)) is r equired cell autonomously for the expression of Pax7 in dorsal cells and Pa x6 in lateral cells. Thus the opb(+) gene product acts intracellularly in t he reception or interpretation of signals that determine cell types in the dorsal 80% of the neural tube. At later stages, the lack of opb(+) causes a non-cell-autonomous expansion of ventral cell types into dorsal regions of the neural tube, revealing that opb(+) controls the production of a diffus ible molecule that defines the domain of Shh expression. The data indicate that opb(+) could act as either a novel component of a dorsalizing pathway or a novel intracellular negative regulator of the Shh signal transduction pathway. (C) 2000 Academic Press.