XB-ART-58504
J Dev Biol
2021 Aug 27;93:. doi: 10.3390/jdb9030034.
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The Role of RNA-Binding Proteins in Vertebrate Neural Crest and Craniofacial Development.
Forman TE
,
Dennison BJC
,
Fantauzzo KA
.
???displayArticle.abstract???
Cranial neural crest (NC) cells delaminate from the neural folds in the forebrain to the hindbrain during mammalian embryogenesis and migrate into the frontonasal prominence and pharyngeal arches. These cells generate the bone and cartilage of the frontonasal skeleton, among other diverse derivatives. RNA-binding proteins (RBPs) have emerged as critical regulators of NC and craniofacial development in mammals. Conventional RBPs bind to specific sequence and/or structural motifs in a target RNA via one or more RNA-binding domains to regulate multiple aspects of RNA metabolism and ultimately affect gene expression. In this review, we discuss the roles of RBPs other than core spliceosome components during human and mouse NC and craniofacial development. Where applicable, we review data on these same RBPs from additional vertebrate species, including chicken, Xenopus and zebrafish models. Knockdown or ablation of several RBPs discussed here results in altered expression of transcripts encoding components of developmental signaling pathways, as well as reduced cell proliferation and/or increased cell death, indicating that these are common mechanisms contributing to the observed phenotypes. The study of these proteins offers a relatively untapped opportunity to provide significant insight into the mechanisms underlying gene expression regulation during craniofacial morphogenesis.
???displayArticle.pubmedLink??? 34564083
???displayArticle.link??? J Dev Biol
???displayArticle.grants??? [+]
F31DE029364 NIDCR NIH HHS, R01DE027689 NIDCR NIH HHS, K02DE028572 NIDCR NIH HHS, F31 DE029364 NIDCR NIH HHS, R01 DE027689 NIDCR NIH HHS, K02 DE028572 NIDCR NIH HHS, T32 GM008497 NIGMS NIH HHS
Species referenced: Xenopus laevis
Genes referenced: cnbp col2a1 ddx3x dlx2 eif4a3 elavl1 elavl4 esrp1 fam50a foxd3 hnrnpk hnrnpu ptbp1 rbfox2 rbmx sox9 srsf3 tbx2 tcof1 tfap2a
GO keywords: neural crest cell migration [+]
???displayArticle.disOnts??? nonsyndromic deafness [+]
X-linked monogenic disease
myotonic dystrophy type 2
specific developmental disorder
pervasive developmental disorder
macrocephaly-autism syndrome
dystonia 16
TARP syndrome
microcephaly
epilepsy
Treacher Collins syndrome
cleft palate
cleft lip
???displayArticle.omims??? TREACHER COLLINS SYNDROME 1; TCS1 [+]
ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES
INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SHASHI TYPE; MRXSSH
INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, ARMFIELD TYPE; MRXSA
FRAGILE X SYNDROME; FXS
INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB
INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB
BASILICATA-AKHTAR SYNDROME; MRXSBA
TARP SYNDROME; TARPS
MYOTONIC DYSTROPHY 2; DM2
DYSTONIA 16; DYT16
AU-KLINE SYNDROME; AUKS
DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 54; DEE54
DEAFNESS, AUTOSOMAL RECESSIVE 109; DFNB109
???attribute.lit??? ???displayArticles.show???
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