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A non-syndromic orofacial cleft risk locus links tRNA splicing defects to neural crest cell pathologies [Ribo-seq]

ABSTRACT: A non-syndromic orofacial cleft risk locus links tRNA splicing defects to neural crest cell pathologies [Ribo-seq]

PROVIDER: PRJNA1122518 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR29358241.fastq.gz	Fastqsanger.gz
	SRR29358242.fastq.gz	Fastqsanger.gz
	SRR29358243.fastq.gz	Fastqsanger.gz
	SRR29358244.fastq.gz	Fastqsanger.gz
	SRR29358245.fastq.gz	Fastqsanger.gz

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Project description:Orofacial clefts are the most common form of congenital craniofacial malformations worldwide. The etiology of these birth defects is multifactorial, involving genetic and environmental factors. In most cases, however, the underlying causes remain unexplained, precluding molecular understanding of disease mechanisms. Here, we integrated genome-wide association data, targeted re-sequencing of case and control cohorts, cell type-specific epigenomic profiling, and genome architecture analyses, to functionally and molecularly dissect a genomic locus associated with an increased risk of non-syndromic orofacial cleft. We found that common and rare risk variants associated with orofacial cleft intersect with a conserved enhancer (e2p24.2) that becomes activated in cranial neural crest cells—the embryonic cell type responsible for sculpting the craniofacial complex. We mapped e2p24.2 long-range interactions to a topologically associated domain harboring MYCN and DDX1 and demonstrated that both MYCN and DDX1 are required for craniofacial development in chicken embryos. We found that e2p24.2 regulates the expression of MYCN, but not DDX1, in cranial neural crest cells. In turn, DDX1 is a target of the MYC family of transcription factors and a component of the tRNA splicing complex. The loss of DDX1 in cranial neural crest cells resulted in the accumulation of unspliced tRNA fragments, depletion of the mature pool of intron-containing tRNAs, and ribosome stalling at codons decoded by these tRNAs. These effects were accompanied by defects in both global protein synthesis and cranial neural crest cell migration. We further showed that the induction of tRNA fragments is sufficient to disrupt craniofacial development. Together, these results uncovered a molecular mechanism in which impaired tRNA splicing affects neural crest and craniofacial development and positioned MYCN, DDX1, and tRNA processing defects as risk factors in the pathogenesis of orofacial clefts.

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A non-syndromic orofacial cleft risk locus links tRNA splicing defects to neural crest cell pathologies [Ribo-seq]

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