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den Hollander, A.I.* ; Koenekoop, R.K.* ; Mohamed, M.D.* ; Arts, H.H.* ; Boldt, K.H.W. ; Towns, K.V.* ; Sedmak, T.* ; Beer, M. ; Nagel-Wolfrum, K.* ; McKibbin, M.* ; Dharmaraj, S.* ; Lopez, I.* ; Ivings, L.* ; Williams, G.A.* ; Springell, K.* ; Woods, C.G.* ; Jafri, H.* ; Rashid, Y.* ; Strom, T.M. ; van der Zwaag, B.* ; Gosens, I.* ; Kersten, F.F.* ; van Wijk, E.* ; Veltman, J.A.* ; Zonneveld, M.N.* ; van Beersum, S.E.* ; Maumenee, I.H.* ; Wolfrum, U.* ; Cheetham, M.E.* ; Ueffing, M. ; Cremers, F.P.* ; Inglehearn, C.F.* ; Roepman, R.*

Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis.

Nat. Genet. 39, 889-895 (2007)
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Leber congenital amaurosis (LCA) causes blindness or severe visual impairment at or within a few months of birth. Here we show, using homozygosity mapping, that the LCA5 gene on chromosome 6q14, which encodes the previously unknown ciliary protein lebercilin, is associated with this disease. We detected homozygous nonsense and frameshift mutations in LCA5 in five families affected with LCA. In a sixth family, the LCA5 transcript was completely absent. LCA5 is expressed widely throughout development, although the phenotype in affected individuals is limited to the eye. Lebercilin localizes to the connecting cilia of photoreceptors and to the microtubules, centrioles and primary cilia of cultured mammalian cells. Using tandem affinity purification, we identified 24 proteins that link lebercilin to centrosomal and ciliary functions. Members of this interactome represent candidate genes for LCA and other ciliopathies. Our findings emphasize the emerging role of disrupted ciliary processes in the molecular pathogenesis of LCA.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
ISSN (print) / ISBN 1061-4036
e-ISSN 1546-1718
Zeitschrift Nature Genetics
Quellenangaben Band: 39, Heft: 7, Seiten: 889-895 Artikelnummer: , Supplement: ,
Verlag Nature Publishing Group
Verlagsort New York, NY
Begutachtungsstatus Peer reviewed