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CiliaCarta: An integrated and validated compendium of ciliary genes.
van Dam, Teunis J P; Kennedy, Julie; van der Lee, Robin; de Vrieze, Erik; Wunderlich, Kirsten A; Rix, Suzanne; Dougherty, Gerard W; Lambacher, Nils J; Li, Chunmei; Jensen, Victor L; Leroux, Michel R; Hjeij, Rim; Horn, Nicola; Texier, Yves; Wissinger, Yasmin; van Reeuwijk, Jeroen; Wheway, Gabrielle; Knapp, Barbara; Scheel, Jan F; Franco, Brunella; Mans, Dorus A; van Wijk, Erwin; Képès, François; Slaats, Gisela G; Toedt, Grischa; Kremer, Hannie; Omran, Heymut; Szymanska, Katarzyna; Koutroumpas, Konstantinos; Ueffing, Marius; Nguyen, Thanh-Minh T; Letteboer, Stef J F; Oud, Machteld M; van Beersum, Sylvia E C; Schmidts, Miriam; Beales, Philip L; Lu, Qianhao; Giles, Rachel H; Szklarczyk, Radek; Russell, Robert B; Gibson, Toby J; Johnson, Colin A; Blacque, Oliver E; Wolfrum, Uwe; Boldt, Karsten; Roepman, Ronald; Hernandez-Hernandez, Victor; Huynen, Martijn A.
Afiliação
  • van Dam TJP; Centre for Molecular and Biomolecular Informatics, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Kennedy J; Theoretical Biology and Bioinformatics, Science faculty, Utrecht University, Utrecht, the Netherlands.
  • van der Lee R; School of Biomolecular and Biomedical Science, University College Dublin, Belfield, Dublin, Ireland.
  • de Vrieze E; Centre for Molecular and Biomolecular Informatics, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Wunderlich KA; Department of Otorhinolaryngology, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Rix S; Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Dougherty GW; Molecular Cell Biology, Institute of Molecular Physiology, Johannes Gutenberg University of Mainz, Mainz, Germany.
  • Lambacher NJ; Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.
  • Li C; Department of General Pediatrics, University Hospital Muenster, Muenster, Germany.
  • Jensen VL; School of Biomolecular and Biomedical Science, University College Dublin, Belfield, Dublin, Ireland.
  • Leroux MR; Department of Molecular Biology and Biochemistry and Centre for Cell Biology, Development and Disease, Simon Fraser University, Burnaby, British Columbia, Canada.
  • Hjeij R; Department of Molecular Biology and Biochemistry and Centre for Cell Biology, Development and Disease, Simon Fraser University, Burnaby, British Columbia, Canada.
  • Horn N; Department of Molecular Biology and Biochemistry and Centre for Cell Biology, Development and Disease, Simon Fraser University, Burnaby, British Columbia, Canada.
  • Texier Y; Department of Molecular Biology and Biochemistry and Centre for Cell Biology, Development and Disease, Simon Fraser University, Burnaby, British Columbia, Canada.
  • Wissinger Y; Department of General Pediatrics, University Hospital Muenster, Muenster, Germany.
  • van Reeuwijk J; Medical Proteome Center, Institute for Ophthalmic Research, University of Tuebingen, Tuebingen, Germany.
  • Wheway G; Medical Proteome Center, Institute for Ophthalmic Research, University of Tuebingen, Tuebingen, Germany.
  • Knapp B; Medical Proteome Center, Institute for Ophthalmic Research, University of Tuebingen, Tuebingen, Germany.
  • Scheel JF; Department of Human Genetics and Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Franco B; Section of Ophthalmology & Neurosciences, Leeds Institute of Molecular Medicine, University of Leeds, Leeds, United Kingdom.
  • Mans DA; Molecular Cell Biology, Institute of Molecular Physiology, Johannes Gutenberg University of Mainz, Mainz, Germany.
  • van Wijk E; Molecular Cell Biology, Institute of Molecular Physiology, Johannes Gutenberg University of Mainz, Mainz, Germany.
  • Képès F; Telethon Institute of Genetics and Medicine (TIGEM), Naples, Italy.
  • Slaats GG; Medical Genetics, Department of Translational Medicine, Federico II University of Naples, Naples, Italy.
  • Toedt G; Department of Human Genetics and Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Kremer H; Department of Otorhinolaryngology, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Omran H; Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Szymanska K; Institute of Systems and Synthetic Biology (iSSB), Genopole, CNRS, Univ. Evry, France.
  • Koutroumpas K; Dept. Nephrology and Hypertension, Regenerative Medicine Center, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Ueffing M; Structural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany.
  • Nguyen TT; Department of Otorhinolaryngology, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Letteboer SJF; Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Oud MM; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.
  • van Beersum SEC; Department of General Pediatrics, University Hospital Muenster, Muenster, Germany.
  • Schmidts M; Section of Ophthalmology & Neurosciences, Leeds Institute of Molecular Medicine, University of Leeds, Leeds, United Kingdom.
  • Beales PL; Institute of Systems and Synthetic Biology (iSSB), Genopole, CNRS, Univ. Evry, France.
  • Lu Q; Medical Proteome Center, Institute for Ophthalmic Research, University of Tuebingen, Tuebingen, Germany.
  • Giles RH; Department of Human Genetics and Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Szklarczyk R; Department of Human Genetics and Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Russell RB; Department of Human Genetics and Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Gibson TJ; Department of Human Genetics and Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Johnson CA; Department of Human Genetics and Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Blacque OE; Pediatric Genetics Division, Center for Pediatrics and Adolescent Medicine, University Hospital Freiburg, Freiburg, Germany.
  • Wolfrum U; Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.
  • Boldt K; Biochemie Zentrum Heidelberg (BZH), Heidelberg University, Heidelberg, Germany.
  • Roepman R; Bioquant/Cell Networks, Heidelberg, Germany.
  • Hernandez-Hernandez V; Dept. Nephrology and Hypertension, Regenerative Medicine Center, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Huynen MA; Centre for Molecular and Biomolecular Informatics, Radboud University Medical Center, Nijmegen, the Netherlands.
PLoS One ; 14(5): e0216705, 2019.
Article em En | MEDLINE | ID: mdl-31095607
ABSTRACT
The cilium is an essential organelle at the surface of mammalian cells whose dysfunction causes a wide range of genetic diseases collectively called ciliopathies. The current rate at which new ciliopathy genes are identified suggests that many ciliary components remain undiscovered. We generated and rigorously analyzed genomic, proteomic, transcriptomic and evolutionary data and systematically integrated these using Bayesian statistics into a predictive score for ciliary function. This resulted in 285 candidate ciliary genes. We generated independent experimental evidence of ciliary associations for 24 out of 36 analyzed candidate proteins using multiple cell and animal model systems (mouse, zebrafish and nematode) and techniques. For example, we show that OSCP1, which has previously been implicated in two distinct non-ciliary processes, causes ciliogenic and ciliopathy-associated tissue phenotypes when depleted in zebrafish. The candidate list forms the basis of CiliaCarta, a comprehensive ciliary compendium covering 956 genes. The resource can be used to objectively prioritize candidate genes in whole exome or genome sequencing of ciliopathy patients and can be accessed at http//bioinformatics.bio.uu.nl/john/syscilia/ciliacarta/.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cílios / Genômica Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cílios / Genômica Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article