Literature DB >> 10769235

Fate and function of the ventral ectodermal ridge during mouse tail development.

D C Goldman1, G R Martin, P P Tam.   

Abstract

In the mouse embryo, the body axis continues to develop after gastrulation as a tail forms at the posterior end of the embryo. Little is known about what controls outgrowth and patterning of the tail, but it has been speculated that the ventral ectodermal ridge (VER), a morphologically distinct ectoderm on the ventral surface near the tip of the tail, is a source of signals that regulate tail development (Grüneberg, H. (1956). Nature 177, 787-788). We tested this hypothesis by ablating all or part of the VER and assessing the effects of such ablations on the development of tail explants cultured in vitro. The data showed that the VER produces signals necessary for somitogenesis in the tail and that the cells that produce these signals are localized in the middle and posterior region of the VER. Dye labeling experiments revealed that cells from these regions move anteriorly within the VER and eventually exit it, thereby colonizing the ventral surface ectoderm anterior to the VER. In situ hybridization analysis showed that the genes encoding the signaling molecules FGF17 and BMP2 are specifically expressed in the VER. Assays for gene expression in VER-ablated and control tails were performed to identify targets of VER signaling. The data showed that the VER is required for expression of the gene encoding the BMP antagonist noggin in the tail ventral mesoderm, leading us to speculate that one of the major functions of the VER in tail development is to regulate BMP activity.

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Year:  2000        PMID: 10769235     DOI: 10.1242/dev.127.10.2113

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  19 in total

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Review 2.  Cellular and molecular mechanisms of regeneration in Xenopus.

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Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2004-05-29       Impact factor: 6.237

3.  The cessation of gastrulation: BMP signaling and EMT during and at the end of gastrulation.

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4.  STELLA-positive subregions of the primitive streak contribute to posterior tissues of the mouse gastrula.

Authors:  Maria M Mikedis; Karen M Downs
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5.  Organization of Embryonic Morphogenesis via Mechanical Information.

Authors:  Dipjyoti Das; Dörthe Jülich; Jamie Schwendinger-Schreck; Emilie Guillon; Andrew K Lawton; Nicolas Dray; Thierry Emonet; Corey S O'Hern; Mark D Shattuck; Scott A Holley
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Review 6.  Birth defects associated with perturbations in preimplantation, gastrulation, and axis extension: from conjoined twinning to caudal dysgenesis.

Authors:  Anna Ferrer-Vaquer; Anna-Katerina Hadjantonakis
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2012-11-26       Impact factor: 5.814

7.  Mouse Crossveinless-2 is the vertebrate homolog of a Drosophila extracellular regulator of BMP signaling.

Authors:  Catherine Coffinier; Nan Ketpura; Uyen Tran; Douglas Geissert; E M De Robertis
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8.  PRDM1/BLIMP1 is widely distributed to the nascent fetal-placental interface in the mouse gastrula.

Authors:  Maria M Mikedis; Karen M Downs
Journal:  Dev Dyn       Date:  2016-11-12       Impact factor: 3.780

Review 9.  New horizons at the caudal embryos: coordinated urogenital/reproductive organ formation by growth factor signaling.

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Journal:  Curr Opin Genet Dev       Date:  2009-09-16       Impact factor: 5.578

10.  Widespread but tissue-specific patterns of interferon-induced transmembrane protein 3 (IFITM3, FRAGILIS, MIL-1) in the mouse gastrula.

Authors:  Maria M Mikedis; Karen M Downs
Journal:  Gene Expr Patterns       Date:  2013-04-29       Impact factor: 1.224

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