Epigenetic regulation of craniofacial development and disease

被引:5
|
作者
Shull, Lomeli C. [1 ]
Artinger, Kristin B. [2 ]
机构
[1] Univ Colorado, Dept Craniofacial Biol, Anschutz Med Campus, Aurora, CO 80045 USA
[2] Univ Minnesota, Sch Dent, Dept Diagnost & Biol Sci, Minneapolis, MN USA
来源
BIRTH DEFECTS RESEARCH | 2024年 / 116卷 / 01期
关键词
chromatin; congenital birth defects; craniofacial; epigenetics; neural crest; COFFIN-SIRIS SYNDROME; DE-NOVO MUTATIONS; BORJESON-FORSSMAN-LEHMANN; RUBINSTEIN-TAYBI SYNDROME; OF-FUNCTION MUTATIONS; HISTONE ACETYLTRANSFERASE KAT6B; LINKED INTELLECTUAL DISABILITY; DNA METHYLTRANSFERASES DNMT3A; CHROMATIN REMODELING COMPLEX; MENTAL-RETARDATION SYNDROME;
D O I
10.1002/bdr2.2271
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
BackgroundThe formation of the craniofacial complex relies on proper neural crest development. The gene regulatory networks (GRNs) and signaling pathways orchestrating this process have been extensively studied. These GRNs and signaling cascades are tightly regulated as alterations to any stage of neural crest development can lead to common congenital birth defects, including multiple syndromes affecting facial morphology as well as nonsyndromic facial defects, such as cleft lip with or without cleft palate. Epigenetic factors add a hierarchy to the regulation of transcriptional networks and influence the spatiotemporal activation or repression of specific gene regulatory cascades; however less is known about their exact mechanisms in controlling precise gene regulation.AimsIn this review, we discuss the role of epigenetic factors during neural crest development, specifically during craniofacial development and how compromised activities of these regulators contribute to congenital defects that affect the craniofacial complex.
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页数:34
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