Comprehensive expression analysis of all Wnt genes and their major secreted antagonists during mouse limb development and cartilage differentiation

被引:172
作者
Witte, Florian [1 ,2 ,3 ]
Dokas, Janine [1 ,2 ]
Neuendorf, Franziska [1 ,2 ]
Mundlos, Stefan [1 ,2 ]
Stricker, Sigmar [1 ,2 ]
机构
[1] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
[2] Charite, Inst Med Genet, D-13353 Berlin, Germany
[3] Free Univ Berlin, Inst Chem Biochem, D-1000 Berlin, Germany
关键词
Limb development; Chondrogenesis; Growth plate; Wnt; Sfrp; Frzb; Dkk; Wisp; Wif1; SIGNALING PATHWAY; HEDGEHOG; SFRP-2; ROLES; MUTATIONS; PATTERNS; CLONING; TARGET; BRAIN; PLAYS;
D O I
10.1016/j.gep.2008.12.009
中图分类号
Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程];
摘要
Wnt signalling plays important roles in patterning and outgrowth of the vertebrate limb. Different mutations in Wnt genes, their antagonists or (co-)receptors result in patterning and outgrowth defects as well as chandrocyte and bone phenotypes in mouse and human. Understanding Wnt activity during mouse limb development and chondrogenesis requires a temporal and spatial overview of Wnt signalling key factor expression. Here we present a comparative expression analysis of all 19 Writ genes and their major secreted antagonists of the Dickkopf (Dkk), Wisp and the secreted frizzled related protein (Sfrp) families during mouse limb development. Our study reveals new domains of expression for Wnt2, Wnt2b, Wnt5b, Wnt6, Wnt7b, Wnt9a, Wnt10a, Wnt10b, Wnt11 and Wnt16, in the limb. We also identified novel expression domains for the Wnt antagonists Sfrp1, Sfrp3, Sfrp5, Wisp1 as well as Dkk2 and Dkk3. We provide a full expression pattern for Wif1 in limb development, for which no limb expression had been documented so far. (c) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:215 / 223
页数:9
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