Hnrnpul1 loss of function affects skeletal and limb development

Blackwell, D. L.; Fraser, S. D.; Caluseriu, O.; Vivori, C.; Gordon, P.; Tyndall, A. V.; Lamont, R. E.; Parboosingh, J. S.; Innes, A. M.; Bernier, F. P.; Childs, S. J.

doi:10.1101/2020.02.04.934257

bioRxiv · 10.1101/2020.02.04.934257

Hnrnpul1 loss of function affects skeletal and limb development

Blackwell, D. L.·Fraser, S. D.·Caluseriu, O.·Vivori, C.·Gordon, P.·Tyndall, A. V.·Lamont, R. E.·Parboosingh, J. S.·Innes, A. M.·Bernier, F. P.·Childs, S. J.

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Abstract

Mutations in RNA binding proteins can lead to pleiotropic phenotypes including craniofacial, skeletal, limb and neurological symptoms. Heterogeneous Nuclear Ribonucleoproteins (hnRNPs) are involved in nucleic acid binding, transcription and splicing through direct binding to DNA and RNA, or through interaction with other proteins in the spliceosome. We show a developmental role for Hnrnpul1 in zebrafish, resulting in reduced craniofacial tendon length, severe adult-onset scoliosis and reduced fin size. We demonstrate a role of Hnrnpul1 in alternative splicing and transcriptional regulation using RNA sequencing. Given its cross-species conservation and role in splicing it would not be surprising if it had a role in human development but the developmental role of this gene in humans has not been explored. Whole exome sequencing detected a frameshift variant in HNRNPUL1 in two siblings with congenital limb malformations which remain variants of unknown significance. Zebrafish Hnrnpul1 mutants suggest an important developmental role of hnRNPUL1 and provide motivation for exploring potential conservation of ancient regulatory circuits involving hnRNPUL1 in human development.

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Blackwell, D. L., Fraser, S. D., Caluseriu, O., Vivori, C., Gordon, P., Tyndall, A. V., Lamont, R. E., Parboosingh, J. S., Innes, A. M., Bernier, F. P., Childs, S. J.. 2020-02-04. Hnrnpul1 loss of function affects skeletal and limb development. https://doi.org/10.1101/2020.02.04.934257

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