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Hox基因在体节中胚层中确定椎骨类型。

Hox genes specify vertebral types in the presomitic mesoderm.

作者信息

Carapuço Marta, Nóvoa Ana, Bobola Nicoletta, Mallo Moisés

机构信息

Instituto Gulbenkian de Ciencia, 2780-156 Oeiras, Portugal.

出版信息

Genes Dev. 2005 Sep 15;19(18):2116-21. doi: 10.1101/gad.338705.

DOI:10.1101/gad.338705
PMID:16166377
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1221883/
Abstract

We show here that expression of Hoxa10 in the presomitic mesoderm is sufficient to confer a Hox group 10 patterning program to the somite, producing vertebrae without ribs, an effect not achieved when Hoxa10 is expressed in the somites. In addition, Hox group 11-dependent vertebral sacralization requires Hoxa11 expression in the presomitic mesoderm, while their caudal differentiation requires that Hoxa11 is expressed in the somites. Therefore, Hox gene patterning activity is different in the somites and presomitic mesoderm, the latter being very prominent for Hox gene-mediated patterning of the axial skeleton. This is further supported by our finding that inactivation of Gbx2, a homeobox-containing gene expressed in the presomitic mesoderm but not in the somites, produced Hox-like phenotypes in the axial skeleton without affecting Hox gene expression.

摘要

我们在此表明,在体节形成前的中胚层中Hoxa10的表达足以赋予体节一个Hox基因10模式程序,从而产生无肋骨的椎骨,而当Hoxa10在体节中表达时则无法实现这一效果。此外,Hox基因11依赖性的椎体骶化需要Hoxa11在体节形成前的中胚层中表达,而它们的尾部分化则要求Hoxa11在体节中表达。因此,Hox基因的模式形成活性在体节和体节形成前的中胚层中有所不同,后者在Hox基因介导的轴向骨骼模式形成中非常突出。我们发现,Gbx2(一个在体节形成前的中胚层而非体节中表达的含同源框基因)的失活在不影响Hox基因表达的情况下,在轴向骨骼中产生了类似Hox的表型,这进一步支持了上述观点。

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本文引用的文献

1
Hoxa2 downregulates Six2 in the neural crest-derived mesenchyme.Hoxa2在神经嵴衍生的间充质中下调Six2。
Development. 2005 Feb;132(3):469-78. doi: 10.1242/dev.01536. Epub 2005 Jan 5.
2
Specification of vertebral identity is coupled to Notch signalling and the segmentation clock.椎体身份的特化与Notch信号传导和体节时钟相关联。
Development. 2004 Mar;131(6):1221-33. doi: 10.1242/dev.01030. Epub 2004 Feb 11.
3
Hox10 and Hox11 genes are required to globally pattern the mammalian skeleton.Hox10和Hox11基因对于构建哺乳动物骨骼的整体模式是必需的。
Science. 2003 Jul 18;301(5631):363-7. doi: 10.1126/science.1085672.
4
Mesenchymal patterning by Hoxa2 requires blocking Fgf-dependent activation of Ptx1.Hoxa2介导的间充质模式形成需要阻断Fgf依赖的Ptx1激活。
Development. 2003 Aug;130(15):3403-14. doi: 10.1242/dev.00554.
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Reversible gene inactivation in the mouse.小鼠中的可逆基因失活
Genomics. 2003 Apr;81(4):356-60. doi: 10.1016/s0888-7543(03)00032-6.
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Cdx1 and Cdx2 have overlapping functions in anteroposterior patterning and posterior axis elongation.Cdx1和Cdx2在前后模式形成和后轴延伸中具有重叠功能。
Development. 2002 May;129(9):2181-93. doi: 10.1242/dev.129.9.2181.
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Localized and transient transcription of Hox genes suggests a link between patterning and the segmentation clock.Hox基因的局部和瞬时转录表明了模式形成与体节时钟之间的联系。
Cell. 2001 Jul 27;106(2):207-17. doi: 10.1016/s0092-8674(01)00436-6.
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Wnt-3a is required for somite specification along the anteroposterior axis of the mouse embryo and for regulation of cdx-1 expression.Wnt-3a对于小鼠胚胎前后轴上体节的特化以及cdx-1表达的调控是必需的。
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Axial skeletal patterning in mice lacking all paralogous group 8 Hox genes.缺乏所有同源异型框8基因旁系同源群的小鼠的轴向骨骼模式形成
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Distinct regulatory elements direct delta1 expression in the nervous system and paraxial mesoderm of transgenic mice.不同的调控元件指导转基因小鼠神经系统和轴旁中胚层中delta1的表达。
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