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Msx1和Osr2的拮抗作用将哺乳动物的牙齿排列成单行。

Antagonistic actions of Msx1 and Osr2 pattern mammalian teeth into a single row.

作者信息

Zhang Zunyi, Lan Yu, Chai Yang, Jiang Rulang

机构信息

Center for Oral Biology and Department of Biomedical Genetics, University of Rochester Medical Center, Rochester, NY 14642, USA.

出版信息

Science. 2009 Feb 27;323(5918):1232-4. doi: 10.1126/science.1167418.

Abstract

Mammals have single-rowed dentitions, whereas many nonmammalian vertebrates have teeth in multiple rows. Neither the molecular mechanism regulating iterative tooth initiation nor that restricting mammalian tooth development in one row is known. We found that mice lacking the transcription factor odd-skipped related-2 (Osr2) develop supernumerary teeth lingual to their molars because of expansion of the odontogenic field. Osr2 was expressed in a lingual-to-buccal gradient and restricted expression of bone morphogenetic protein 4 (Bmp4), an essential odontogenic signal, in the developing tooth mesenchyme. Expansion of odontogenic field in Osr2-deficient mice required Msx1, a feedback activator of Bmp4 expression. These findings suggest that the Bmp4-Msx1 pathway propagates mesenchymal activation for sequential tooth induction and that spatial modulation of this pathway provides a mechanism for patterning vertebrate dentition.

摘要

哺乳动物具有单排牙列,而许多非哺乳动物脊椎动物有多排牙齿。目前,调控牙齿迭代起始的分子机制以及限制哺乳动物牙齿排成一排发育的分子机制均不为人知。我们发现,缺乏转录因子odd-skipped related-2(Osr2)的小鼠由于牙源性区域的扩展,在其磨牙舌侧长出了额外的牙齿。Osr2在舌侧至颊侧呈梯度表达,并限制了骨形态发生蛋白4(Bmp4,一种重要的牙源性信号)在发育中的牙齿间充质中的表达。Osr2缺陷小鼠牙源性区域的扩展需要Msx1,它是Bmp4表达的反馈激活因子。这些发现表明,Bmp4-Msx1通路传播间充质激活以进行连续的牙齿诱导,并且该通路的空间调节为脊椎动物牙列的模式形成提供了一种机制。

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