Gene-Environment Interplay and MicroRNAs in Cleft Lip and Cleft Palate.
Junichi IwataPublished in: Oral science international (2020)
Cleft lip (CL) with/without cleft palate (CP) (hereafter CL/P) is the second most common congenital birth defect, affecting 7.94 to 9.92 children per 10,000 live births worldwide, followed by Down syndrome. An increasing number of genes have been identified as affecting susceptibility and/or as causative genes for CL/P in mouse genetic and chemically-induced CL and CP studies, as well as in human genome-wide association studies and linkage analysis. While marked progress has been made in the identification of genetic and environmental risk factors for CL/P, the interplays between these factors are not yet fully understood. This review aims to summarize our current knowledge of CL and CP from genetically engineered mouse models and environmental factors that have been studied in mice. Understanding the regulatory mechanism(s) of craniofacial development may not only advance our understanding of craniofacial developmental biology, but could also provide approaches for the prevention of birth defects and for tissue engineering in craniofacial tissue regeneration.
Keyphrases
- genome wide
- tissue engineering
- copy number
- dna methylation
- genome wide association
- endothelial cells
- stem cells
- gestational age
- bioinformatics analysis
- healthcare
- mouse model
- case control
- gene expression
- adipose tissue
- preterm birth
- insulin resistance
- drug induced
- hiv infected
- induced pluripotent stem cells
- hiv testing
- pluripotent stem cells