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发育肢体中Wnt-1的表达与生长及骨骼模式异常的相关性。

Correlation of expression of Wnt-1 in developing limbs with abnormalities in growth and skeletal patterning.

作者信息

Zákány J, Duboule D

机构信息

European Molecular Biology Laboratory, Heidelberg, Germany.

出版信息

Nature. 1993 Apr 8;362(6420):546-9. doi: 10.1038/362546a0.

Abstract

The Wnt genes are members of a family of vertebrate genes related to the Drosophila gene wingless (wg). They encode secreted molecules that are thought to be important in patterning and growth control during ontogenesis. Several such genes are transcribed in localized domains during limb budding and morphogenesis. We report here a congenital limb malformation in a mouse transgenic line that ectopically expresses Wnt-1 in the developing limbs. The hemizygote phenotype, which is inherited as an autosomal dominant trait, presents extensive distal truncations of skeletal elements, skeletal fusions and interdigital webbing. The data shown here demonstrate that abnormal Wnt-1 expression is correlated with retarded mesenchymal condensations replaced by highly proliferative cells in the limb bud. This seems to lead to an inability of the affected cells to participate in normal skeletal development leading to the adult defects.

摘要

Wnt基因是与果蝇无翅基因(wg)相关的脊椎动物基因家族的成员。它们编码分泌分子,这些分子被认为在个体发育过程中的模式形成和生长控制中很重要。在肢体萌芽和形态发生过程中,有几个这样的基因在局部区域转录。我们在此报告了一个小鼠转基因品系中的先天性肢体畸形,该品系在发育中的肢体中异位表达Wnt-1。半合子表型作为常染色体显性性状遗传,表现为骨骼元素的广泛远端截断、骨骼融合和指间蹼。此处所示数据表明,异常的Wnt-1表达与肢体芽中被高度增殖细胞取代的间充质凝聚延迟相关。这似乎导致受影响的细胞无法参与正常的骨骼发育,从而导致成年期缺陷。

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