2011
DOI: 10.1242/dev.057505
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Dlx5 and Dlx6 expression in the anterior neural fold is essential for patterning the dorsal nasal capsule

Abstract: SUMMARYMorphogenesis of the vertebrate facial skeleton depends upon inductive interactions between cephalic neural crest cells (CNCCs) and cephalic epithelia. The nasal capsule is a CNCC-derived cartilaginous structure comprising a ventral midline bar (mesethmoid) overlaid by a dorsal capsule (ectethmoid). Although Shh signalling from the anterior-most region of the endoderm (EZ-I) patterns the mesethmoid, the cues involved in ectethmoid induction are still undefined. Here, we show that ectethmoid formation de… Show more

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Cited by 20 publications
(16 citation statements)
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“…In particular, the MSX1 and DLX5 homeotic genes also appear to play pivotal roles in this gene network as they establish functional interactions with many of the candidates shown in Figure 3 . Interestingly, MSX genes control the spatial organization of the NC-derived craniofacial skeleton [Khadka et al, 2006;Han et al, 2007;Gitton et al, 2011;Attanasio et al, 2013]. Also DLX homeobox genes function in early NC development, and in the late specification of NC-derived structures [McLarren et al, 2003;Ruest et al, 2003], and they play key roles in skull and brain development [Jones and Rubinstein, 2004;Kraus and Lufkin, 2006;Vincentz et al, 2016].…”
Section: Functional Implication and Biological Interpretation Of Domementioning
confidence: 99%
“…In particular, the MSX1 and DLX5 homeotic genes also appear to play pivotal roles in this gene network as they establish functional interactions with many of the candidates shown in Figure 3 . Interestingly, MSX genes control the spatial organization of the NC-derived craniofacial skeleton [Khadka et al, 2006;Han et al, 2007;Gitton et al, 2011;Attanasio et al, 2013]. Also DLX homeobox genes function in early NC development, and in the late specification of NC-derived structures [McLarren et al, 2003;Ruest et al, 2003], and they play key roles in skull and brain development [Jones and Rubinstein, 2004;Kraus and Lufkin, 2006;Vincentz et al, 2016].…”
Section: Functional Implication and Biological Interpretation Of Domementioning
confidence: 99%
“…Many of these genes are known candidates for ASD, including DLX5 and DLX6 (reviewed above), FGFR2, MSX1, POLR1A , and PTCH1 . Both DLX5 and DLX6 are indeed required for NC-derived facial morphogenesis (Gitton et al, 2011) FGFRs are among the main craniosynostosis-associated genes. In particular, gain-of-function mutations in FGFR2 are typically associated to Apert (OMIM#101200) and Crouzon (OMIM#123500) syndromes, while both FGFR1 and FGFR2 are found mutated in Pfeiffer syndrome (OMIM#101600) (Lattanzi et al, 2012).…”
Section: Asd and The Genetics Of The Domestication Syndromementioning
confidence: 99%
“…Miscommunication between these midline signaling centers leads to midline facial defects such as holoprosencephaly and hypertelorism as seen in humans and many other vertebrate species. In the frontonasal region, the anterior neural fold ectoderm has also been found to signal to the underlying ectomesenchyme to pattern the ectethmoid (dorsal) portion of the nasal capsule (Gitton et al 2011) in avians. In contrast, the underlying mesethmoid cartilage of the avian nasal capsule is induced by endodermal Hedgehog signaling from the foregut (Benouaiche et al 2008).…”
Section: Hedgehog Signalingmentioning
confidence: 99%