Literature DB >> 21087601

Ectodermal Wnt/β-catenin signaling shapes the mouse face.

Bethany S Reid1, Hui Yang, Vida Senkus Melvin, Makoto M Taketo, Trevor Williams.   

Abstract

The canonical Wnt/β-catenin pathway is an essential component of multiple developmental processes. To investigate the role of this pathway in the ectoderm during facial morphogenesis, we generated conditional β-catenin mouse mutants using a novel ectoderm-specific Cre recombinase transgenic line. Our results demonstrate that ablating or stabilizing β-catenin in the embryonic ectoderm causes dramatic changes in facial morphology. There are accompanying alterations in the expression of Fgf8 and Shh, key molecules that establish a signaling center critical for facial patterning, the frontonasal ectodermal zone (FEZ). These data indicate that Wnt/β-catenin signaling within the ectoderm is critical for facial development and further suggest that this pathway is an important mechanism for generating the diverse facial shapes of vertebrates during evolution.
Copyright © 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 21087601      PMCID: PMC3057077          DOI: 10.1016/j.ydbio.2010.11.012

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  40 in total

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2.  Generation and characterization of a novel neural crest marker allele, Inka1-LacZ, reveals a role for Inka1 in mouse neural tube closure.

Authors:  Bethany S Reid; Thomas D Sargent; Trevor Williams
Journal:  Dev Dyn       Date:  2010-04       Impact factor: 3.780

3.  Intestinal polyposis in mice with a dominant stable mutation of the beta-catenin gene.

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4.  The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.

Authors:  L Nanni; J E Ming; M Bocian; K Steinhaus; D W Bianchi; C Die-Smulders; A Giannotti; K Imaizumi; K L Jones; M D Campo; R A Martin; P Meinecke; M E Pierpont; N H Robin; I D Young; E Roessler; M Muenke
Journal:  Hum Mol Genet       Date:  1999-12       Impact factor: 6.150

5.  Cre-mediated gene inactivation demonstrates that FGF8 is required for cell survival and patterning of the first branchial arch.

Authors:  A Trumpp; M J Depew; J L Rubenstein; J M Bishop; G R Martin
Journal:  Genes Dev       Date:  1999-12-01       Impact factor: 11.361

6.  Ectodermal Wnt function as a neural crest inducer.

Authors:  Martín I García-Castro; Christophe Marcelle; Marianne Bronner-Fraser
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7.  Spatial and temporal analysis of gene expression during growth and fusion of the mouse facial prominences.

Authors:  Weiguo Feng; Sonia M Leach; Hannah Tipney; Tzulip Phang; Mark Geraci; Richard A Spritz; Lawrence E Hunter; Trevor Williams
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8.  FGF4, a direct target of LEF1 and Wnt signaling, can rescue the arrest of tooth organogenesis in Lef1(-/-) mice.

Authors:  Klaus Kratochwil; Juan Galceran; Sabine Tontsch; Wera Roth; Rudolf Grosschedl
Journal:  Genes Dev       Date:  2002-12-15       Impact factor: 11.361

9.  Inactivation of the beta-catenin gene by Wnt1-Cre-mediated deletion results in dramatic brain malformation and failure of craniofacial development.

Authors:  V Brault; R Moore; S Kutsch; M Ishibashi; D H Rowitch; A P McMahon; L Sommer; O Boussadia; R Kemler
Journal:  Development       Date:  2001-04       Impact factor: 6.868

10.  A role for frizzled 3 in neural crest development.

Authors:  M A Deardorff; C Tan; J P Saint-Jeannet; P S Klein
Journal:  Development       Date:  2001-10       Impact factor: 6.868

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  48 in total

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2.  Signals from the brain induce variation in avian facial shape.

Authors:  Diane Hu; Nathan M Young; Qiuping Xu; Heather Jamniczky; Rebecca M Green; Washington Mio; Ralph S Marcucio; Benedikt Hallgrimsson
Journal:  Dev Dyn       Date:  2015-08-10       Impact factor: 3.780

Review 3.  Receptor tyrosine kinase signaling: regulating neural crest development one phosphate at a time.

Authors:  Katherine A Fantauzzo; Philippe Soriano
Journal:  Curr Top Dev Biol       Date:  2015-01-20       Impact factor: 4.897

4.  ISLET1-Dependent β-Catenin/Hedgehog Signaling Is Required for Outgrowth of the Lower Jaw.

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Journal:  Mol Cell Biol       Date:  2017-03-31       Impact factor: 4.272

5.  A conserved Pbx-Wnt-p63-Irf6 regulatory module controls face morphogenesis by promoting epithelial apoptosis.

Authors:  Elisabetta Ferretti; Bingsi Li; Rediet Zewdu; Victoria Wells; Jean M Hebert; Courtney Karner; Matthew J Anderson; Trevor Williams; Jill Dixon; Michael J Dixon; Michael J Depew; Licia Selleri
Journal:  Dev Cell       Date:  2011-10-06       Impact factor: 12.270

6.  The molecular anatomy of mammalian upper lip and primary palate fusion at single cell resolution.

Authors:  Hong Li; Kenneth L Jones; Joan E Hooper; Trevor Williams
Journal:  Development       Date:  2019-06-17       Impact factor: 6.868

7.  Cell and Tissue Scale Forces Coregulate Fgfr2-Dependent Tetrads and Rosettes in the Mouse Embryo.

Authors:  Jun Wen; Hirotaka Tao; Kimberly Lau; Haijiao Liu; Craig A Simmons; Yu Sun; Sevan Hopyan
Journal:  Biophys J       Date:  2017-05-23       Impact factor: 4.033

8.  Anisotropic stress orients remodelling of mammalian limb bud ectoderm.

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Journal:  Nat Cell Biol       Date:  2015-04-20       Impact factor: 28.824

9.  Association of WNT9B Gene Polymorphisms With Nonsyndromic Cleft Lip With or Without Cleft Palate in Brazilian Nuclear Families.

Authors:  Clarissa Fontoura; Renato M Silva; José M Granjeiro; Ariadne Letra
Journal:  Cleft Palate Craniofac J       Date:  2015-01

10.  Distinct populations within Isl1 lineages contribute to appendicular and facial skeletogenesis through the β-catenin pathway.

Authors:  Ryutaro Akiyama; Hiroko Kawakami; M Mark Taketo; Sylvia M Evans; Naoyuki Wada; Anna Petryk; Yasuhiko Kawakami
Journal:  Dev Biol       Date:  2014-01-11       Impact factor: 3.582

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