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Prdm1a 在斑马鱼神经嵴特化过程中直接激活 foxd3 和 tfap2a。

Prdm1a directly activates foxd3 and tfap2a during zebrafish neural crest specification.

机构信息

Department of Craniofacial Biology, School of Dental Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.

出版信息

Development. 2013 Aug;140(16):3445-55. doi: 10.1242/dev.096164.


DOI:10.1242/dev.096164
PMID:23900542
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3737723/
Abstract

The neural crest comprises multipotent precursor cells that are induced at the neural plate border by a series of complex signaling and genetic interactions. Several transcription factors, termed neural crest specifiers, are necessary for early neural crest development; however, the nature of their interactions and regulation is not well understood. Here, we have established that the PR/SET domain-containing transcription factor Prdm1a is co-expressed with two essential neural crest specifiers, foxd3 and tfap2a, at the neural plate border. Through rescue experiments, chromatin immunoprecipitation and reporter assays, we have determined that Prdm1a directly binds to and transcriptionally activates enhancers for foxd3 and tfap2a and that they are functional, direct targets of Prdm1a at the neural plate border. Additionally, analysis of dominant activator and dominant repressor Prdm1a constructs suggests that Prdm1a is required both as a transcriptional activator and transcriptional repressor for neural crest development in zebrafish embryos.

摘要

神经嵴由多能前体细胞组成,这些前体细胞在神经板边缘受到一系列复杂的信号和遗传相互作用的诱导。一些转录因子,称为神经嵴特化因子,对于早期神经嵴发育是必需的;然而,它们的相互作用和调控的本质尚不清楚。在这里,我们已经确定 PR/SET 结构域包含的转录因子 Prdm1a 与两个必需的神经嵴特化因子 foxd3 和 tfap2a 在神经板边缘共同表达。通过挽救实验、染色质免疫沉淀和报告基因分析,我们已经确定 Prdm1a 直接结合并转录激活 foxd3 和 tfap2a 的增强子,并且它们是 Prdm1a 在神经板边缘的功能性直接靶标。此外,对显性激活子和显性抑制子 Prdm1a 构建体的分析表明,Prdm1a 对于斑马鱼胚胎的神经嵴发育既需要作为转录激活因子,也需要作为转录抑制因子。

相似文献

[1]
Prdm1a directly activates foxd3 and tfap2a during zebrafish neural crest specification.

Development. 2013-8

[2]
Tfap2a and Foxd3 regulate early steps in the development of the neural crest progenitor population.

Dev Biol. 2011-9-22

[3]
prdm1a Regulates sox10 and islet1 in the development of neural crest and Rohon-Beard sensory neurons.

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[4]
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[5]
Highlighted article: "prdm1a regulates sox10 and islet1 in the development of neural crest and Rohon-Beard sensory neurons" by E.C. Olesnicky, L. Hernandez-Lagunas, K.B. Artinger.

Genesis. 2010-11

[6]
prdm1a functions upstream of itga5 in zebrafish craniofacial development.

Genesis. 2015

[7]
prdm1a and olig4 act downstream of Notch signaling to regulate cell fate at the neural plate border.

Dev Biol. 2011-6-13

[8]
CHD7, Oct3/4, Sox2, and Nanog control FoxD3 expression during mouse neural crest-derived stem cell formation.

FEBS J. 2016-10

[9]
An evolutionarily conserved kernel of gata5, gata6, otx2 and prdm1a operates in the formation of endoderm in zebrafish.

Dev Biol. 2011-7-1

[10]
Transcriptional control of Rohon-Beard sensory neuron development at the neural plate border.

Dev Dyn. 2009-4

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prdm1a drives a fate switch between hair cells of different mechanosensory organs.

Nat Commun. 2025-8-18

[2]
Reactivation of an embryonic cardiac neural crest transcriptional profile during zebrafish heart regeneration.

Proc Natl Acad Sci U S A. 2025-6-24

[3]
drives a fate switch between hair cells of different mechanosensory organs.

bioRxiv. 2025-6-3

[4]
Reactivation of an Embryonic Cardiac Neural Crest Transcriptional Subcircuit During Zebrafish Heart Regeneration.

bioRxiv. 2025-1-17

[5]
Genetic and Developmental Divergence in the Neural Crest Program between Cichlid Fish Species.

Mol Biol Evol. 2024-11-1

[6]
Genetic and developmental divergence in the neural crest programme between cichlid fish species.

bioRxiv. 2024-6-7

[7]
PRDM1 DNA-binding zinc finger domain is required for normal limb development and is disrupted in split hand/foot malformation.

Dis Model Mech. 2023-4-1

[8]
Shoc2 controls ERK1/2-driven neural crest development by balancing components of the extracellular matrix.

Dev Biol. 2022-12

[9]
NRG1/ErbB signalling controls the dialogue between macrophages and neural crest-derived cells during zebrafish fin regeneration.

Nat Commun. 2021-11-3

[10]
Single-cell RNA analysis identifies pre-migratory neural crest cells expressing markers of differentiated derivatives.

Elife. 2021-8-16

本文引用的文献

[1]
Dynamic and differential regulation of stem cell factor FoxD3 in the neural crest is Encrypted in the genome.

PLoS Genet. 2012-12-20

[2]
Redundant roles of PRDM family members in zebrafish craniofacial development.

Dev Dyn. 2012-11-14

[3]
BMP, Wnt and FGF signals are integrated through evolutionarily conserved enhancers to achieve robust expression of Pax3 and Zic genes at the zebrafish neural plate border.

Development. 2012-10-3

[4]
The Prdm family: expanding roles in stem cells and development.

Development. 2012-7

[5]
Novel Tfap2-mediated control of soxE expression facilitated the evolutionary emergence of the neural crest.

Development. 2012-1-12

[6]
Tfap2a and Foxd3 regulate early steps in the development of the neural crest progenitor population.

Dev Biol. 2011-9-22

[7]
Ancestral network module regulating prdm1 expression in the lamprey neural plate border.

Dev Dyn. 2011-8-25

[8]
Prdm1a and miR-499 act sequentially to restrict Sox6 activity to the fast-twitch muscle lineage in the zebrafish embryo.

Development. 2011-8-31

[9]
prdm1a and olig4 act downstream of Notch signaling to regulate cell fate at the neural plate border.

Dev Biol. 2011-6-13

[10]
Neural crest stem cell multipotency requires Foxd3 to maintain neural potential and repress mesenchymal fates.

Development. 2011-1-12

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