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Publication : Craniofacial Defects in Embryos with Homozygous Deletion of <i>Eftud2</i> in Their Neural Crest Cells Are Not Rescued by <i>Trp53</i> Deletion.

First Author  Beauchamp MC Year  2022
Journal  Int J Mol Sci Volume  23
Issue  16 PubMed ID  36012294
Mgi Jnum  J:327815 Mgi Id  MGI:7334088
Doi  10.3390/ijms23169033 Citation  Beauchamp MC, et al. (2022) Craniofacial Defects in Embryos with Homozygous Deletion of Eftud2 in Their Neural Crest Cells Are Not Rescued by Trp53 Deletion. Int J Mol Sci 23(16)
abstractText  Embryos with homozygous mutation of Eftud2 in their neural crest cells (Eftud2(ncc-/-)) have brain and craniofacial malformations, hyperactivation of the P53-pathway and die before birth. Treatment of Eftud2(ncc-/-) embryos with pifithrin-alpha, a P53-inhibitor, partly improved brain and craniofacial development. To uncover if craniofacial malformations and death were indeed due to P53 hyperactivation we generated embryos with homozygous loss of function mutations in both Eftud2 and Trp53 in the neural crest cells. We evaluated the molecular mechanism underlying craniofacial development in pifithrin-alpha-treated embryos and in Eftud2; Trp53 double homozygous (Eftud2(ncc-/-); Trp53(ncc-/-)) mutant embryos. Eftud2(ncc-/-) embryos that were treated with pifithrin-alpha or homozygous mutant for Trp53 in their neural crest cells showed reduced apoptosis in their neural tube and reduced P53-target activity. Furthermore, although the number of SOX10 positive cranial neural crest cells was increased in embryonic day (E) 9.0 Eftud2(ncc-/-); Trp53(ncc-/-) embryos compared to Eftud2(ncc-/-) mutants, brain and craniofacial development, and survival were not improved in double mutant embryos. Furthermore, mis-splicing of both P53-regulated transcripts, Mdm2 and Foxm1, and a P53-independent transcript, Synj2bp, was increased in the head of Eftud2(ncc-/-); Trp53(ncc-/-) embryos. While levels of Zmat3, a P53- regulated splicing factor, was similar to those of wild-type. Altogether, our data indicate that both P53-regulated and P53-independent pathways contribute to craniofacial malformations and death of Eftud2(ncc-/-) embryos.
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