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Cacheiro, P.* ; Muñoz-Fuentes, V.* ; Murray, S.A.* ; Dickinson, M.E.* ; Bucan, M.* ; Nutter, L.M.J.* ; Peterson, K.A.* ; Haselimashhadi, H.* ; Flenniken, A.M.* ; Morgan, H.* ; Westerberg, H.* ; Konopka, T.* ; Hsu, C.W.* ; Christiansen, A.V.* ; Lanza, D.G.* ; Beaudet, A.L.* ; Heaney, J.D.* ; Fuchs, H. ; Gailus-Durner, V. ; Sorg, T.* ; Prochazka, J.* ; Novosadova, V.* ; Lelliott, C.J.* ; Wardle-Jones, H.* ; Wells, S.* ; Teboul, L.* ; Cater, H.* ; Stewart, M.* ; Hough, T.* ; Wurst, W. ; Sedlacek, R.* ; Adams, D.J.* ; Seavitt, J.R.* ; Tocchini-Valentini, G.* ; Mammano, F.* ; Braun, R.E.* ; McKerlie, C.* ; Herault, Y.* ; Hrabě de Angelis, M. ; Mallon, A.M.* ; Lloyd, K.C.K.* ; Brown, S.D.M.* ; Parkinson, H.* ; Meehan, T.F.* ; Smedley, D.* ; International Mouse Phenotyping Consortium (Marschall, S. ; Lengger, C. ; Maier, H. ; Seisenberger, C. ; Bürger, A. ; Kühn, R. ; Schick, J. ; Hörlein, A. ; Oritz, O. ; Giesert, F. ; Beig, J.)

Human and mouse essentiality screens as a resource for disease gene discovery.

Nat. Commun. 11:655 (2020)
Postprint Forschungsdaten DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
The identification of causal variants in sequencing studies remains a considerable challenge that can be partially addressed by new gene-specific knowledge. Here, we integrate measures of how essential a gene is to supporting life, as inferred from viability and phenotyping screens performed on knockout mice by the International Mouse Phenotyping Consortium and essentiality screens carried out on human cell lines. We propose a cross-species gene classification across the Full Spectrum of Intolerance to Loss-of-function (FUSIL) and demonstrate that genes in five mutually exclusive FUSIL categories have differing biological properties. Most notably, Mendelian disease genes, particularly those associated with developmental disorders, are highly overrepresented among genes non-essential for cell survival but required for organism development. After screening developmental disorder cases from three independent disease sequencing consortia, we identify potentially pathogenic variants in genes not previously associated with rare diseases. We therefore propose FUSIL as an efficient approach for disease gene discovery.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Sprache englisch
Veröffentlichungsjahr 2020
HGF-Berichtsjahr 2020
ISSN (print) / ISBN 2041-1723
e-ISSN 2041-1723
Zeitschrift Nature Communications
Quellenangaben Band: 11, Heft: 1, Seiten: , Artikelnummer: 655 Supplement: ,
Verlag Nature Publishing Group
Verlagsort London
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Experimental Genetics (IEG)
Institute of Developmental Genetics (IDG)
POF Topic(s) 30201 - Metabolic Health
30204 - Cell Programming and Repair
Forschungsfeld(er) Genetics and Epidemiology
PSP-Element(e) G-500600-001
G-500500-001
G-500692-001
DOI 10.1038/s41467-020-14284-2
WOS ID WOS:000513245600040
Scopus ID 85078825003
PubMed ID 32005800
Erfassungsdatum 2020-03-26
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