Dworkin Sebastian, Simkin Johanna, Darido Charbel, Partridge Darren D, Georgy Smitha R, Caddy Jacinta, Wilanowski Tomasz, Lieschke Graham J, Doggett Karen, Heath Joan K, Jane Stephen M
Department of Medicine, Monash University Central Clinical School, Prahran, VIC 3181, Australia.
Walter and Eliza Hall Institute of Medical Research, 1G Royal Parade, Parkville, VIC 3050, Australia.
Mech Dev. 2014 Aug;133:77-90. doi: 10.1016/j.mod.2014.05.005. Epub 2014 Jun 7.
Craniofacial development is a highly conserved process that requires complex interactions between neural crest cells (NCCs) and pharyngeal tissues derived from all three germ layers. Signals emanating from the pharyngeal endoderm drive differentiation of NCCs into craniofacial cartilage, and disruption of this process underpins several human craniofacial defects (CFD). Here, we demonstrate that morpholino (MO)-mediated knockdown in zebrafish of the highly conserved transcription factor grainyhead-like 3 (grhl3), which is selectively expressed in the pharyngeal endoderm, leads to severe hypoplasia of the lower jaw cartilages. Phylogenetic analysis of conserved grhl-binding sites in gene regulatory regions identified endothelin-1 (edn1) as a putative direct grhl3 target gene, and this was confirmed by chromatin precipitation (ChIP) assays in zebrafish embryos. Injection of sub-phenotypic concentrations of MOs targeting both grhl3 and edn1 induced jaw abnormalities, and injection of edn1 mRNA into grhl3-morphants rescued both pharyngeal expression of the downstream effectors of edn1, and jaw cartilage formation. This study sheds new light on the role of endodermal endothelin-1 in vertebrate jaw development, and highlights potential new genetic defects that could underpin human CFD.
颅面发育是一个高度保守的过程,需要神经嵴细胞(NCCs)与源自所有三个胚层的咽组织之间进行复杂的相互作用。咽内胚层发出的信号驱动NCCs分化为颅面软骨,这一过程的破坏是几种人类颅面缺陷(CFD)的基础。在此,我们证明,在斑马鱼中,通过吗啉代(MO)介导敲低在咽内胚层中选择性表达的高度保守转录因子颗粒头样3(grhl3),会导致下颌软骨严重发育不全。对基因调控区域中保守的grhl结合位点进行系统发育分析,确定内皮素-1(edn1)为推定的grhl3直接靶基因,斑马鱼胚胎中的染色质沉淀(ChIP)分析证实了这一点。注射针对grhl3和edn1的亚表型浓度的MO会诱导颌骨异常,而向grhl3突变体注射edn1 mRNA可挽救edn1下游效应物的咽部表达以及颌骨软骨形成。这项研究为内胚层内皮素-1在脊椎动物颌骨发育中的作用提供了新的线索,并突出了可能是人类CFD基础的潜在新基因缺陷。