POLR1B and neural crest cell anomalies in Treacher Collins syndrome type 4

Elodie Sanchez, Beryl Laplace-Builhe, Frederic Tran Mau-Them, Eric Richard, Alice Goldenberg, Tomi L. Toler, Thomas Guignard, Vincent Gatinois, Marie Vincent, Catherine Blanchet, Anne Boland, Marie Therese Bihoreau, Jean-Francois Deleuze, Robert Olaso, Walton Nephi, Hermann-Josef Luedecke, Joke B. G. M. Verheij, Florence Moreau-Lenoir, Francoise Denoyelle, Jean-Baptiste RiviereJean-Louis Laplanche, Marcia Willing, Guillaume Captier, Florence Apparailly*, Dagmar Wieczorek, Corinne Collet, Farida Djouad, David Genevieve

*Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

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    Purpose Treacher Collins syndrome (TCS) is a rare autosomal dominant mandibulofacial dysostosis, with a prevalence of 0.2-1/10,000. Features include bilateral and symmetrical malar and mandibular hypoplasia and facial abnormalities due to abnormal neural crest cell (NCC) migration and differentiation. To date, three genes have been identified: TCOF1, POLR1C, and POLR1D. Despite a large number of patients with a molecular diagnosis, some remain without a known genetic anomaly. Methods We performed exome sequencing for four individuals with TCS but who were negative for pathogenic variants in the known causative genes. The effect of the pathogenic variants was investigated in zebrafish. Results We identified three novel pathogenic variants in POLR1B. Knockdown of polr1b in zebrafish induced an abnormal craniofacial phenotype mimicking TCS that was associated with altered ribosomal gene expression, massive p53-associated cellular apoptosis in the neuroepithelium, and reduced number of NCC derivatives. Conclusion Pathogenic variants in the RNA polymerase I subunit POLR1B might induce massive p53-dependent apoptosis in a restricted neuroepithelium area, altering NCC migration and causing cranioskeletal malformations. We identify POLR1B as a new causative gene responsible for a novel TCS syndrome (TCS4) and establish a novel experimental model in zebrafish to study POLR1B-related TCS.

    Original languageEnglish
    Pages (from-to)547-556
    Number of pages10
    JournalGenetics in Medicine
    Issue number3
    Publication statusPublished - Mar-2020


    • Treacher Collins-Franceschetti
    • POLR1B
    • apoptosis
    • neural crest cells
    • TOOLS
    • P53

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