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脊椎动物后脑节段模式形成的分子机制。

Molecular mechanisms of segmental patterning in the vertebrate hindbrain.

作者信息

Wilkinson D G

机构信息

MRC Laboratory of Eukaryotic Molecular Genetics, National Institute for Medical Research, London, UK.

出版信息

Perspect Dev Neurobiol. 1993;1(3):117-25.

PMID:7916256
Abstract

The finding that pattern formation in the vertebrate hindbrain occurs through a process of segmentation raises the question of the underlying molecular mechanisms. A number of genes have been implicated in this pattern through their segment-restricted expression, and the function and possible regulatory relationships of these are discussed. There is now strong evidence that certain Hox genes are involved in specifying hindbrain segments and neural crest derivatives that contribute to cranial ganglia and the branchial arches. It is likely that retinoic acid receptors either directly or indirectly regulate Hox gene expression in the hindbrain. The zinc finger gene Krox-20 controls the segment-restricted up-regulation of at least one Hox gene, Hox-B2. Studies of the Krox-20 gene reveal a progressive sharpening of its expression domains that reflect cellular interactions leading to segment formation. A receptor tyrosine kinase gene, Sek, has been implicated in such cellular interactions by its rhombomeric expression pattern. In addition, this receptor kinase may be involved in mesoderm segmentation.

摘要

脊椎动物后脑的模式形成是通过分段过程实现的这一发现,引发了关于其潜在分子机制的问题。许多基因因其在分段区域的特异性表达而与这种模式相关,本文将讨论这些基因的功能以及可能的调控关系。目前有充分的证据表明,某些Hox基因参与确定后脑节段以及对脑神经节和鳃弓有贡献的神经嵴衍生物。视黄酸受体很可能直接或间接地调节后脑Hox基因的表达。锌指基因Krox-20控制至少一种Hox基因Hox-B2在分段区域的上调表达。对Krox-20基因的研究揭示了其表达域的逐渐细化,这反映了导致节段形成的细胞间相互作用。一种受体酪氨酸激酶基因Sek,因其在菱脑节中的表达模式而与这种细胞间相互作用有关。此外,这种受体激酶可能参与中胚层的分段。

相似文献

1
Molecular mechanisms of segmental patterning in the vertebrate hindbrain.脊椎动物后脑节段模式形成的分子机制。
Perspect Dev Neurobiol. 1993;1(3):117-25.
2
Molecular mechanisms of segmental patterning in the vertebrate hindbrain and neural crest.脊椎动物后脑和神经嵴节段模式形成的分子机制。
Bioessays. 1993 Aug;15(8):499-505. doi: 10.1002/bies.950150802.
3
Retinoic acid alters hindbrain Hox code and induces transformation of rhombomeres 2/3 into a 4/5 identity.视黄酸改变后脑Hox编码,并诱导菱脑节2/3转变为4/5身份。
Nature. 1992;360(6406):737-41. doi: 10.1038/360737a0.
4
Genetic control of segmentation in the vertebrate hindbrain.脊椎动物后脑节段化的遗传控制。
Perspect Dev Neurobiol. 1995;3(1):29-38.
5
[Role of the Krox-20 gene in the development of rhombencephalon].[Krox-20基因在菱脑发育中的作用]
C R Seances Soc Biol Fil. 1997;191(1):91-4.
6
Progressive spatial restriction of Sek-1 and Krox-20 gene expression during hindbrain segmentation.后脑分割过程中Sek-1和Krox-20基因表达的渐进性空间限制。
Dev Biol. 1996 Jan 10;173(1):26-38. doi: 10.1006/dbio.1996.0004.
7
Homeobox genes and models for patterning the hindbrain and branchial arches.同源异型盒基因与后脑和鳃弓模式形成的模型
Dev Suppl. 1991;1:187-96.
8
The expression pattern of the mouse receptor tyrosine kinase gene MDK1 is conserved through evolution and requires Hoxa-2 for rhombomere-specific expression in mouse embryos.小鼠受体酪氨酸激酶基因MDK1的表达模式在进化过程中是保守的,并且在小鼠胚胎中,其菱脑节特异性表达需要Hoxa-2。
Dev Biol. 1996 Aug 1;177(2):397-412. doi: 10.1006/dbio.1996.0173.
9
Hox genes and segmentation of the vertebrate hindbrain.Hox基因与脊椎动物后脑的分节
Curr Top Dev Biol. 2009;88:103-37. doi: 10.1016/S0070-2153(09)88004-6.
10
Overexpression of thyroid hormone receptor alpha 1 during zebrafish embryogenesis disrupts hindbrain patterning and implicates retinoic acid receptors in the control of hox gene expression.甲状腺激素受体α1在斑马鱼胚胎发育过程中的过表达会破坏后脑模式,并表明视黄酸受体参与hox基因表达的调控。
Differentiation. 1999 Jul;65(1):1-11. doi: 10.1046/j.1432-0436.1999.6510001.x.

引用本文的文献

1
Why Does the Face Predict the Brain? Neural Crest Induction, Craniofacial Morphogenesis, and Neural Circuit Development.为何面部能预示大脑?神经嵴诱导、颅面形态发生与神经回路发育。
Front Physiol. 2020 Dec 11;11:610970. doi: 10.3389/fphys.2020.610970. eCollection 2020.
2
Hoxb1 functions in both motoneurons and in tissues of the periphery to establish and maintain the proper neuronal circuitry.Hoxb1在运动神经元和外周组织中都发挥作用,以建立和维持适当的神经回路。
Genes Dev. 2004 Jul 1;18(13):1539-52. doi: 10.1101/gad.1207204. Epub 2004 Jun 15.
3
Hoxb-2 transcriptional activation in rhombomeres 3 and 5 requires an evolutionarily conserved cis-acting element in addition to the Krox-20 binding site.
除了Krox-20结合位点外,菱脑节3和5中Hoxb-2的转录激活还需要一个进化上保守的顺式作用元件。
EMBO J. 1996 Oct 1;15(19):5383-96.