Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome.

TitleFunctional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome.
Publication TypeJournal Article
Year of Publication2015
AuthorsRoosing, 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
JournalElife
Volume4
Paginatione06602
Date Published2015 May 30
ISSN2050-084X
KeywordsAbnormalities, 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.

DOI10.7554/eLife.06602
Alternate JournalElife
PubMed ID26026149
PubMed Central IDPMC4477441
Grant List260888 / / 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