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Prdm1a 对于斑马鱼咽后弓的发育是必需的。

Prdm1a is necessary for posterior pharyngeal arch development in zebrafish.

机构信息

Department of Biomedical and Pharmaceutical Sciences, University of Montana, Center for Structural and Functional Neuroscience, Missoula, Montana, USA.

出版信息

Dev Dyn. 2009 Oct;238(10):2575-87. doi: 10.1002/dvdy.22090.


DOI:10.1002/dvdy.22090
PMID:19777590
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2832216/
Abstract

Multiple tissue interactions and signaling within the pharyngeal arches are required for development of the craniofacial skeleton. Here, we focus on the role of the transcription factor prdm1a in the differentiation of the posterior skeleton. prdm1a is expressed in the presumptive pharyngeal arch region and later in an endodermal pouch, the otic vesicle, and pharyngeal teeth. prdm1a mutants display a reduction in pharyngeal arch markers, a loss of posterior ceratobranchial cartilages, and a reduction in most neural crest-derived dermal bones. This is likely caused by a decrease in the number of proliferating cells but not an increase in cell death. Finally, a reduction in two key developmental signaling pathways, Fgf and retinoic acid, alters prdm1a expression, suggesting that prdm1a expression is mediated by these signaling pathways to pattern the posterior craniofacial skeleton. Together, these results indicate an essential role for prdm1a in the development of the zebrafish craniofacial skeleton.

摘要

多个组织间的相互作用和信号传递在咽弓的发育中对于颅面骨骼的形成是必需的。在这里,我们重点关注转录因子 prdm1a 在后部骨骼分化中的作用。prdm1a 在假定的咽弓区域表达,随后在一个内胚层囊,即听泡和咽齿中表达。prdm1a 突变体显示咽弓标记物减少,后鳃软骨减少,大多数神经嵴衍生的真皮骨减少。这可能是由于增殖细胞数量减少,而不是细胞死亡增加所致。最后,两种关键的发育信号通路,Fgf 和视黄酸的减少改变了 prdm1a 的表达,表明 prdm1a 的表达是由这些信号通路介导的,以模式化后部颅面骨骼。总之,这些结果表明 prdm1a 在斑马鱼颅面骨骼发育中具有重要作用。

相似文献

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[2]
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[3]
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[4]
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[4]
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[6]
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[7]
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[8]
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[9]
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[10]
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Biol Rev Camb Philos Soc. 2022-2

本文引用的文献

[1]
Development of the cranium and paired fins in the zebrafish Danio rerio (Ostariophysi, Cyprinidae).

J Morphol. 1996-8

[2]
A role for chemokine signaling in neural crest cell migration and craniofacial development.

Dev Biol. 2009-9-1

[3]
Transcriptional control of Rohon-Beard sensory neuron development at the neural plate border.

Dev Dyn. 2009-4

[4]
barx1 is necessary for ectomesenchyme proliferation and osteochondroprogenitor condensation in the zebrafish pharyngeal arches.

Dev Biol. 2008-9-1

[5]
Prdm1- and Sox6-mediated transcriptional repression specifies muscle fibre type in the zebrafish embryo.

EMBO Rep. 2008-7

[6]
Expression of multiple slow myosin heavy chain genes reveals a diversity of zebrafish slow twitch muscle fibres with differing requirements for Hedgehog and Prdm1 activity.

Development. 2008-6

[7]
The emergence of ectomesenchyme.

Dev Dyn. 2008-3

[8]
Blimp1 regulates development of the posterior forelimb, caudal pharyngeal arches, heart and sensory vibrissae in mice.

Development. 2007-12

[9]
Cranial neural crest and development of the head skeleton.

Adv Exp Med Biol. 2006

[10]
Blimp-1 is an essential component of the genetic program controlling development of the pectoral limb bud.

Dev Biol. 2006-12-15

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