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

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 RM
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 JE
Valente EM
Kim J
Gleeson JG
Source :
ELife [Elife] 2015 May 30; Vol. 4, pp. e06602. Date of Electronic Publication: 2015 May 30.
Publication Year :
2015

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.

Details

Language :
English
ISSN :
2050-084X
Volume :
4
Database :
MEDLINE
Journal :
ELife
Publication Type :
Academic Journal
Accession number :
26026149
Full Text :
https://doi.org/10.7554/eLife.06602