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配对样同源盒基因MHox是多个谱系骨骼发生早期事件所必需的。

The paired-like homeo box gene MHox is required for early events of skeletogenesis in multiple lineages.

作者信息

Martin J F, Bradley A, Olson E N

机构信息

Department of Biochemistry and Molecular Biology, University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.

出版信息

Genes Dev. 1995 May 15;9(10):1237-49. doi: 10.1101/gad.9.10.1237.

Abstract

Formation of cartilage and bone involves sequential processes in which undifferentiated mesenchyme aggregates into primordial condensations that subsequently grow and differentiate, eventually forming the adult skeleton. Although much has been learned about the structural molecules that compose cartilage and bone, little is known about the nuclear factors that regulate chondrogenesis and osteogenesis. MHox is a homeo box-containing gene that is expressed in the mesenchyme of facial, limb, and vertebral skeletal precursors during mouse embryogenesis. MHox expression has been shown to require epithelial-derived signals, suggesting that MHox may regulate the epithelial-mesenchymal interactions required for skeletal organogenesis. To determine the functions of MHox, we generated a loss-of-function mutation in the MHox gene. Mice homozygous for a mutant MHox allele die soon after birth and exhibit defects of skeletogenesis, involving the loss or malformation of craniofacial, limb, and vertebral skeletal structures. The affected skeletal elements are derived from the cranial neural crest, as well as somitic and lateral mesoderm. Analysis of the mutant phenotype during ontogeny demonstrated a defect in the formation and growth of chondrogenic and osteogenic precursors. These findings provide evidence that MHox regulates the formation of preskeletal condensations from undifferentiated mesenchyme.

摘要

软骨和骨的形成涉及一系列过程,其中未分化的间充质聚集形成原始凝块,这些凝块随后生长并分化,最终形成成年骨骼。尽管人们已经对构成软骨和骨的结构分子有了很多了解,但对于调节软骨生成和骨生成的核因子却知之甚少。MHox是一个含有同源框的基因,在小鼠胚胎发育过程中,它在面部、肢体和椎骨骨骼前体的间充质中表达。研究表明,MHox的表达需要上皮来源的信号,这表明MHox可能调节骨骼器官发生所需的上皮-间充质相互作用。为了确定MHox的功能,我们在MHox基因中产生了功能缺失突变。纯合突变MHox等位基因的小鼠在出生后不久死亡,并表现出骨骼发生缺陷,包括颅面、肢体和椎骨骨骼结构的缺失或畸形。受影响的骨骼元素来自颅神经嵴以及体节和侧中胚层。对个体发育过程中突变表型的分析表明,软骨生成和骨生成前体的形成和生长存在缺陷。这些发现提供了证据,证明MHox调节未分化间充质形成骨骼前凝块的过程。

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