Department of Biology, Virginia Commonwealth University, Richmond, VA, USA.
Department of Public Health Sciences, University of Virginia School of Medicine, Charlottesville, VA, USA.
BMC Genomics. 2018 Nov 3;19(1):795. doi: 10.1186/s12864-018-5186-8.
Development of the face and mouth is orchestrated by a large number of transcription factors, signaling pathways and epigenetic regulators. While we know many of these regulators, our understanding of how they interact with each other and implement changes in gene expression during orofacial development is still in its infancy. Therefore, this study focuses on uncovering potential cooperation between transcriptional regulators and one important signaling pathway, retinoic acid, during development of the midface.
Transcriptome analyses was performed on facial tissues deficient for retinoic acid receptor function at two time points in development; early (35 hpf) just after the neural crest migrates and facial tissues are specified and later (60 hpf) when the mouth has formed and facial structures begin to differentiate. Functional and network analyses revealed that retinoic acid signaling could cooperate with novel epigenetic factors and calcium-NFAT signaling during early orofacial development. At the later stage, retinoic acid may work with WNT and BMP and regulate homeobox containing transcription factors. Finally, there is an overlap in genes dysregulated in Xenopus embryos with median clefts with human genes associated with similar orofacial defects.
This study uncovers novel signaling pathways required for orofacial development as well as pathways that could interact with retinoic acid signaling during the formation of the face. We show that frog faces are an important tool for studying orofacial development and birth defects.
面部和口腔的发育是由大量转录因子、信号通路和表观遗传调控因子协调控制的。虽然我们已经了解了其中的许多调控因子,但我们对于它们如何相互作用并在口面发育过程中实现基因表达的变化的理解还处于起步阶段。因此,本研究专注于揭示转录调控因子与一种重要的信号通路——视黄酸在中面发育过程中的潜在合作关系。
在发育的两个时间点(早期,即神经嵴迁移和面部组织特化后 35 hpf;晚期,即口形成和面部结构开始分化后 60 hpf),对缺乏视黄酸受体功能的面部组织进行了转录组分析。功能和网络分析揭示了视黄酸信号在早期口面发育过程中可以与新型表观遗传因子和钙-NFAT 信号协同作用。在晚期,视黄酸可能与 WNT 和 BMP 一起作用,并调节同源盒转录因子。最后,在具有中线裂的非洲爪蟾胚胎中失调的基因与人类中与类似口面缺陷相关的基因存在重叠。
本研究揭示了口面发育所必需的新的信号通路,以及在面部形成过程中可能与视黄酸信号相互作用的通路。我们表明,青蛙的面部是研究口面发育和出生缺陷的重要工具。