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Msx同源框基因家族与颅面发育

Msx homeobox gene family and craniofacial development.

作者信息

Alappat Sylvia, Zhang Zun Yi, Chen Yi Ping

机构信息

Division of Developmental Biology, Department of Cell and Molecular Biology, Tulane University, New orleans, LA 70118, USA.

出版信息

Cell Res. 2003 Dec;13(6):429-42. doi: 10.1038/sj.cr.7290185.

Abstract

Vertebrate Msx genes are unlinked, homeobox-containing genes that bear homology to the Drosophila muscle segment homeobox gene. These genes are expressed at multiple sites of tissue-tissue interactions during vertebrate embryonic development. Inductive interactions mediated by the Msx genes are essential for normal craniofacial, limb and ectodermal organ morphogenesis, and are also essential to survival in mice, as manifested by the phenotypic abnormalities shown in knockout mice and in humans. This review summarizes studies on the expression, regulation, and functional analysis of Msx genes that bear relevance to craniofacial development in humans and mice. Key words: Msx genes, craniofacial, tooth, cleft palate, suture, development, transcription factor, signaling molecule.

摘要

脊椎动物的Msx基因是不连锁的、含有同源异型框的基因,与果蝇的肌肉节段同源异型框基因具有同源性。这些基因在脊椎动物胚胎发育过程中的多个组织-组织相互作用位点表达。由Msx基因介导的诱导相互作用对于正常的颅面、肢体和外胚层器官形态发生至关重要,对小鼠的生存也至关重要,这在基因敲除小鼠和人类中表现出的表型异常中得到体现。本综述总结了与人类和小鼠颅面发育相关的Msx基因的表达、调控及功能分析研究。关键词:Msx基因、颅面、牙齿、腭裂、缝合线、发育、转录因子、信号分子。

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