prechordal plate
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Author(s):  
José Luis Ferran ◽  
Manuel Irimia ◽  
Luis Puelles

This essay re-examines the singular case of the supposedly unique rostrally elongated notochord described classically in amphioxus. We start from our previous observations in hpf 21 larvae [Albuixech-Crespo et al., 2017] indicating that the brain vesicle has rostrally a rather standard hypothalamic molecular configuration. This correlates with the notochord across a possible rostromedian acroterminal hypothalamic domain . The notochord shows some molecular differences that specifically characterize its pre-acroterminal extension beyond its normal rostral end under the mamillary region. We explored an alternative interpretation that the putative extension of this notochord actually represents a variant form of the prechordal plate in amphioxus, some of whose cells would adopt the notochordal typology, but would lack notochordal patterning properties, and might have some (but not all) prechordal ones instead. We survey in detail the classic and recent literature on gastrulation, prechordal plate and notochord formation in amphioxus, compared the observed patterns with those of some other vertebrates of interest, and re-examine the literature on differential gene expression patterns in this rostralmost area of the head. We noted that previous literature failed at identifying the amphioxus prechordal primordia at appropriate stages. Under this interpretation, a consistent picture can be drawn for cephalochordates, tunicates, and vertebrates. Moreover, there is little evidence for an intrinsic capacity of the early notochord to grow rostralwards (it normally elongates caudalwards). Altogether, we conclude that the hypothesis of a prechordal nature of the elongated amphioxus notochord is consistent with the evidence presented.


eLife ◽  
2021 ◽  
Vol 10 ◽  
Author(s):  
Shaun Abrams ◽  
Jeremy F Reiter

Craniofacial defects are among the most common phenotypes caused by ciliopathies, yet the developmental and molecular etiology of these defects is poorly understood. We investigated multiple mouse models of human ciliopathies (including Tctn2, Cc2d2a and Tmem231 mutants) and discovered that each displays hypotelorism, a narrowing of the midface. As early in development as the end of gastrulation, Tctn2 mutants displayed reduced activation of the Hedgehog (HH) pathway in the prechordal plate, the head organizer. This prechordal plate defect preceded a reduction of HH pathway activation and Shh expression in the adjacent neurectoderm. Concomitant with the reduction of HH pathway activity, Tctn2 mutants exhibited increased cell death in the neurectoderm and facial ectoderm, culminating in a collapse of the facial midline. Enhancing HH signaling by decreasing the gene dosage of a negative regulator of the pathway, Ptch1, decreased cell death and rescued the midface defect in both Tctn2 and Cc2d2a mutants. These results reveal that ciliary HH signaling mediates communication between the prechordal plate and the neurectoderm to provide cellular survival cues essential for development of the facial midline.


2021 ◽  
Author(s):  
Shaun R Abrams ◽  
Jeremy F Reiter

Craniofacial defects are among the most common phenotypes caused by ciliopathies, yet the developmental and molecular etiology of these defects is poorly understood. We investigated multiple mouse models of human ciliopathies (including Tctn2, Cc2d2a and Tmem231 mutants) and discovered that each displays hypotelorism, a narrowing of the midface. As early in development as the end of gastrulation, Tctn2 mutants displayed reduced activation of the Hedgehog (HH) pathway in the prechordal plate, the head organizer. This prechordal plate defect preceded a reduction of HH pathway activation and Shh expression in the adjacent neurectoderm. Concomitant with the reduction of HH pathway activity, Tctn2 mutants exhibited increased cell death in the neurectoderm and facial ectoderm, culminating in a collapse of the facial midline. Enhancing HH signaling by decreasing the gene dosage of a negative regulator of the pathway, Ptch1, decreased cell death and rescued the midface defect in both Tctn2 and Cc2d2a mutants. These results reveal that ciliary HH signaling mediates communication between the prechordal plate and the neurectoderm to provide cellular survival cues essential for development of the facial midline.


2018 ◽  
Vol 441 (2) ◽  
pp. 221-234 ◽  
Author(s):  
Xiaoyun Ren ◽  
Noémie Hamilton ◽  
Ferenc Müller ◽  
Yoshiyuki Yamamoto
Keyword(s):  

2015 ◽  
Vol 89 (1-2) ◽  
pp. 22-30 ◽  
Author(s):  
Dmitri A. Bessarab ◽  
Sinnakaruppan Mathavan ◽  
C. Michael Jones ◽  
N. Ray Dunn

Development ◽  
2014 ◽  
Vol 141 (22) ◽  
pp. 4332-4342 ◽  
Author(s):  
T. Zhang ◽  
C. Yin ◽  
L. Qiao ◽  
L. Jing ◽  
H. Li ◽  
...  
Keyword(s):  

2012 ◽  
Vol 365 (2) ◽  
pp. 350-362 ◽  
Author(s):  
Alice H. Reis ◽  
Karla L. Almeida-Coburn ◽  
Mariana P. Louza ◽  
Débora M. Cerqueira ◽  
Diego P. Aguiar ◽  
...  

2009 ◽  
Vol 327 (1) ◽  
pp. 106-120 ◽  
Author(s):  
Kazushi Aoto ◽  
Yayoi Shikata ◽  
Hajime Imai ◽  
Daisuke Matsumaru ◽  
Tomoyuki Tokunaga ◽  
...  

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