{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,25]],"date-time":"2026-10-25T05:22:26Z","timestamp":1792905746842,"version":"4.5.0"},"reference-count":41,"publisher":"The Company of Biologists","issue":"11","license":[{"start":{"date-parts":[[2025,11,24]],"date-time":"2025-11-24T00:00:00Z","timestamp":1763942400000},"content-version":"vor","delay-in-days":23,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0"}],"funder":[{"DOI":"10.13039\/501100001659","name":"Deutsche Forschungsgemeinschaft","doi-asserted-by":"crossref","award":["BO 1978\/7-3"],"award-info":[{"award-number":["BO 1978\/7-3"]}],"id":[{"id":"10.13039\/501100001659","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/501100001659","name":"Deutsche Forschungsgemeinschaft","doi-asserted-by":"crossref","award":["PA 2030\/5-3"],"award-info":[{"award-number":["PA 2030\/5-3"]}],"id":[{"id":"10.13039\/501100001659","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/100008967","name":"Philipps Universit\u00e4t Marburg","doi-asserted-by":"crossref","id":[{"id":"10.13039\/100008967","id-type":"DOI","asserted-by":"crossref"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2025,11,1]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>We recently identified a rare complex syndrome with craniofacial malformations caused by truncating variants in fibrosin-like 1 (FBRSL1). To investigate the function of Fbrsl1 in craniofacial development, we used the Xenopus laevis model to study the cranial neural crest (NC). While Fbrsl1 was largely dispensable for NC induction and early migration, its loss of function impaired NC differentiation and cartilage formation. This was accompanied by increased expression of p53 and cleaved caspase-3, as well as by exon skipping in the mdm2 gene, a negative regulator of p53. Fbrsl1 may directly affect splicing of mdm2, as we find that FBRSL1 interacts with the splicing factor SF3B1. Notably, pharmacological inhibition of p53 partially rescued the craniofacial phenotype, suggesting that p53-mediated apoptosis underlies the NC defects caused by loss of Fbrsl1 function.<\/jats:p>","DOI":"10.1242\/dmm.052472","type":"journal-article","created":{"date-parts":[[2025,11,24]],"date-time":"2025-11-24T12:36:36Z","timestamp":1763987796000},"source":"Crossref","is-referenced-by-count":3,"title":["Fbrsl1 is required for cranial neural crest development and reflects a conserved function of the human disease-associated protein"],"prefix":"10.1242","volume":"18","author":[{"given":"Sarah","family":"Gerstner","sequence":"first","affiliation":[{"name":"Philipps-University Marburg 1 Department of Biology, Molecular Embryology , , 35043 Marburg ,","place":["Germany"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hanna","family":"Berger-Santangelo","sequence":"additional","affiliation":[{"name":"Philipps-University Marburg 1 Department of Biology, Molecular Embryology , , 35043 Marburg ,","place":["Germany"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gina","family":"Kastens","sequence":"additional","affiliation":[{"name":"Institute of Human Genetics, University Medical Center G\u00f6ttingen 2 , Heinrich-D\u00fcker-Weg 12, 37073 G\u00f6ttingen ,","place":["Germany"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tamara","family":"Scholtes","sequence":"additional","affiliation":[{"name":"Philipps-University Marburg 1 Department of Biology, Molecular Embryology , , 35043 Marburg ,","place":["Germany"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Stella","family":"W\u00e4schenbach","sequence":"additional","affiliation":[{"name":"Philipps-University Marburg 1 Department of Biology, Molecular Embryology , , 35043 Marburg ,","place":["Germany"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-9899-9590","authenticated-orcid":false,"given":"Silke","family":"Pauli","sequence":"additional","affiliation":[{"name":"Institute of Human Genetics, University Medical Center G\u00f6ttingen 2 , Heinrich-D\u00fcker-Weg 12, 37073 G\u00f6ttingen ,","place":["Germany"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2524-5384","authenticated-orcid":false,"given":"Annette","family":"Borchers","sequence":"additional","affiliation":[{"name":"Philipps-University Marburg 1 Department of Biology, Molecular Embryology , , 35043 Marburg ,","place":["Germany"]}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"237","published-online":{"date-parts":[[2025,11,24]]},"reference":[{"key":"2025112407363267600_DMM052472C1","doi-asserted-by":"publisher","first-page":"dmm049544","DOI":"10.1242\/dmm.049544","article-title":"Snrpb is required in murine neural crest cells for proper splicing and craniofacial morphogenesis","volume":"15","author":"Alam","year":"2022","journal-title":"Dis. 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