Cell death in cranial neural crest development

1992 ◽  
Vol 185 (6) ◽  
Author(s):  
Pete Jeffs ◽  
Karen Jaques ◽  
Mark Osmond
2019 ◽  
Vol 69 ◽  
pp. 176-189 ◽  
Author(s):  
Yuqi Yan ◽  
Xiao-tan Zhang ◽  
Guang Wang ◽  
Xin Cheng ◽  
Yu Yan ◽  
...  

2011 ◽  
Vol 356 (1) ◽  
pp. 238-239 ◽  
Author(s):  
Crystal Rogers ◽  
Marianne Bronner-Fraser

2021 ◽  
Vol 15 ◽  
Author(s):  
Rachel A. Keuls ◽  
Ronald J. Parchem

Neural crest development involves a series of dynamic, carefully coordinated events that result in human disease when not properly orchestrated. Cranial neural crest cells acquire unique multipotent developmental potential upon specification to generate a broad variety of cell types. Studies of early mammalian neural crest and nervous system development often use the Cre-loxP system to lineage trace and mark cells for further investigation. Here, we carefully profile the activity of two common neural crest Cre-drivers at the end of neurulation in mice. RNA sequencing of labeled cells at E9.5 reveals that Wnt1-Cre2 marks cells with neuronal characteristics consistent with neuroepithelial expression, whereas Sox10-Cre predominantly labels the migratory neural crest. We used single-cell mRNA and single-cell ATAC sequencing to profile the expression of Wnt1 and Sox10 and identify transcription factors that may regulate the expression of Wnt1-Cre2 in the neuroepithelium and Sox10-Cre in the migratory neural crest. Our data identify cellular heterogeneity during cranial neural crest development and identify specific populations labeled by two Cre-drivers in the developing nervous system.


2014 ◽  
Vol 132 ◽  
pp. 38-43 ◽  
Author(s):  
Paola Betancur ◽  
Marcos Simões-Costa ◽  
Tatjana Sauka-Spengler ◽  
Marianne E. Bronner

2013 ◽  
Vol 381 (1) ◽  
pp. 83-96 ◽  
Author(s):  
Zhidan Xia ◽  
Xiangjun Tong ◽  
Fang Liang ◽  
Yihan Zhang ◽  
Chikin Kuok ◽  
...  

2021 ◽  
Vol 36 (1) ◽  
Author(s):  
Haiyang Li ◽  
Denglu Long ◽  
Guohua Lv ◽  
Xin Cheng ◽  
Guang Wang ◽  
...  

Development ◽  
2000 ◽  
Vol 127 (13) ◽  
pp. 2873-2882 ◽  
Author(s):  
R.A. Cornell ◽  
J.S. Eisen

We examined the role of Delta signaling in specification of two derivatives in zebrafish neural plate: Rohon-Beard spinal sensory neurons and neural crest. deltaA-expressing Rohon-Beard neurons are intermingled with premigratory neural crest cells in the trunk lateral neural plate. Embryos homozygous for a point mutation in deltaA, or with experimentally reduced delta signalling, have supernumerary Rohon-Beard neurons, reduced trunk-level expression of neural crest markers and lack trunk neural crest derivatives. Fin mesenchyme, a putative trunk neural crest derivative, is present in deltaA mutants, suggesting it segregates from other neural crest derivatives as early as the neural plate stage. Cranial neural crest derivatives are also present in deltaA mutants, revealing a genetic difference in regulation of trunk and cranial neural crest development.


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