Title | Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome. |
Publication Type | Journal Article |
Year of Publication | 2015 |
Authors | Roosing, S, Hofree, M, Kim, S, Scott, E, Copeland, B, Romani, M, Silhavy, JL, Rosti, RO, Schroth, J, Mazza, T, Miccinilli, E, Zaki, MS, Swoboda, KJ, Milisa-Drautz, J, Dobyns, WB, Mikati, MA, İncecik, F, Azam, M, Borgatti, R, Romaniello, R, Boustany, R-M, Clericuzio, CL, D'Arrigo, S, Strømme, P, Boltshauser, E, Stanzial, F, Mirabelli-Badenier, M, Moroni, I, Bertini, E, Emma, F, Steinlin, M, Hildebrandt, F, Johnson, CA, Freilinger, M, Vaux, KK, Gabriel, SB, Aza-Blanc, P, Heynen-Genel, S, Ideker, T, Dynlacht, BD, Lee, JEun, Valente, EMaria, Kim, J, Gleeson, JG |
Journal | Elife |
Volume | 4 |
Pagination | e06602 |
Date Published | 2015 May 30 |
ISSN | 2050-084X |
Keywords | Abnormalities, Multiple, Cell Cycle Proteins, Cerebellum, Eye Abnormalities, Gene Frequency, Genetic Predisposition to Disease, Genetic Testing, Genome-Wide Association Study, Heterozygote, Humans, Kidney Diseases, Cystic, Mutant Proteins, Retina, RNA, Small Interfering |
Abstract | Defective primary ciliogenesis or cilium stability forms the basis of human ciliopathies, including Joubert syndrome (JS), with defective cerebellar vermis development. We performed a high-content genome-wide small interfering RNA (siRNA) screen to identify genes regulating ciliogenesis as candidates for JS. We analyzed results with a supervised-learning approach, using SYSCILIA gold standard, Cildb3.0, a centriole siRNA screen and the GTex project, identifying 591 likely candidates. Intersection of this data with whole exome results from 145 individuals with unexplained JS identified six families with predominantly compound heterozygous mutations in KIAA0586. A c.428del base deletion in 0.1% of the general population was found in trans with a second mutation in an additional set of 9 of 163 unexplained JS patients. KIAA0586 is an orthologue of chick Talpid3, required for ciliogenesis and Sonic hedgehog signaling. Our results uncover a relatively high frequency cause for JS and contribute a list of candidates for future gene discoveries in ciliopathies. |
DOI | 10.7554/eLife.06602 |
Alternate Journal | Elife |
PubMed ID | 26026149 |
PubMed Central ID | PMC4477441 |
Grant List | 260888 / / European Research Council / International U54 HG003067 / HG / NHGRI NIH HHS / United States P30NS047101 / NS / NINDS NIH HHS / United States 1R01HD069647-03 / HD / NICHD NIH HHS / United States R01NS048453 / NS / NINDS NIH HHS / United States P30 NS047101 / NS / NINDS NIH HHS / United States R01DK068306 / DK / NIDDK NIH HHS / United States U54HG003067 / HG / NHGRI NIH HHS / United States R01 NS050375 / NS / NINDS NIH HHS / United States R01 NS041537 / NS / NINDS NIH HHS / United States R01 NS048453 / NS / NINDS NIH HHS / United States P03NS047101 / NS / NINDS NIH HHS / United States U54HG006504 / HG / NHGRI NIH HHS / United States U54 HG006504 / HG / NHGRI NIH HHS / United States GGP13146 / / Telethon / Italy R01 DK068306 / DK / NIDDK NIH HHS / United States R01 NS052455 / NS / NINDS NIH HHS / United States P01 HD070494 / HD / NICHD NIH HHS / United States / / Howard Hughes Medical Institute / United States R01 HD069647 / HD / NICHD NIH HHS / United States MR/M000532/1 / / Medical Research Council / United Kingdom R01DK068308 / DK / NIDDK NIH HHS / United States P01HD070494 / HD / NICHD NIH HHS / United States R01NS041537 / NS / NINDS NIH HHS / United States R01NS052455 / NS / NINDS NIH HHS / United States |