Functional characterization of putative cilia genes by high-content analysis

被引:66
作者
Lai, Cary K. [1 ]
Gupta, Nidhi [1 ]
Wen, Xiaohui [1 ]
Rangell, Linda [2 ]
Chih, Ben [1 ]
Peterson, Andrew S. [1 ]
Bazan, J. Fernando [3 ]
Li, Li [4 ]
Scales, Suzie J. [1 ]
机构
[1] Genentech Inc, Dept Mol Biol, San Francisco, CA 94080 USA
[2] Genentech Inc, Dept Pathol, San Francisco, CA 94080 USA
[3] Genentech Inc, Dept Prot Engn & Struct Biol, San Francisco, CA 94080 USA
[4] Genentech Inc, Dept Bioinformat, San Francisco, CA 94080 USA
关键词
INTRAFLAGELLAR TRANSPORT PROTEINS; PROTEOMIC ANALYSIS; SONIC HEDGEHOG; REPRESSOR FUNCTIONS; COUPLED-RECEPTORS; SENSORY ORGANELLE; CELLS ANTENNA; DISEASE GENE; MOUSE; MEMBRANE;
D O I
10.1091/mbc.E10-07-0596
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cilia are microtubule-based protrusions from the cell surface that are involved in a number of essential signaling pathways, yet little is known about many of the proteins that regulate their structure and function. A number of putative cilia genes have been identified by proteomics and comparative sequence analyses, but functional data are lacking for the vast majority. We therefore monitored the effects in three cell lines of small interfering RNA (siRNA) knockdown of 40 of these genes by high-content analysis. We assayed cilia number, length, and transport of two different cargoes (membranous serotonin receptor 6-green fluorescent protein [HTR6-GFP] and the endogenous Hedgehog [Hh] pathway transcription factor Gli3) by immunofluorescence microscopy; and cilia function using a Gli-luciferase Hh signaling assay. Hh signaling was most sensitive to perturbations, with or without visible structural cilia defects. Validated hits include Ssa2 and mC21orf2 with ciliation defects; Ift46 with short cilia; Ptpdc1 and Iqub with elongated cilia; and Arl3, Nme7, and Ssna1 with distinct ciliary transport but not length defects. Our data confirm various ciliary roles for several ciliome proteins and show it is possible to uncouple ciliary cargo transport from cilia formation in vertebrates.
引用
收藏
页码:1104 / 1119
页数:16
相关论文
共 82 条
[1]   ODA16 aids axonemal outer row dynein assembly through an interaction with the intraflagellar transport machinery [J].
Ahmed, Noveera T. ;
Gao, Chunlei ;
Lucker, Ben F. ;
Cole, Douglas G. ;
Mitchell, David R. .
JOURNAL OF CELL BIOLOGY, 2008, 183 (02) :313-322
[2]   Decoding cilia function: Defining specialized genes required for compartmentalized cilia biogenesis [J].
Avidor-Reiss, T ;
Maer, AM ;
Koundakjian, E ;
Polyanovsky, A ;
Keil, T ;
Subramaniam, S ;
Zuker, CS .
CELL, 2004, 117 (04) :527-539
[3]   The ciliopathies: An emerging class of human genetic disorders [J].
Badano, Jose L. ;
Mitsuma, Norimasa ;
Beales, Phil L. ;
Katsanis, Nicholas .
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, 2006, 7 :125-148
[4]   The TROVE module: A common element in telomerase, Ro and Vault ribonucleoproteins [J].
Bateman, A ;
Kickhoefer, V .
BMC BIOINFORMATICS, 2003, 4 (1)
[5]   Identification of ciliary localization sequences within the third intracellular loop of G protein-coupled receptors [J].
Berbari, Nicolas F. ;
Johnson, Andrew D. ;
Lewis, Jacqueline S. ;
Askwith, Candice C. ;
Mykytyn, Kirk .
MOLECULAR BIOLOGY OF THE CELL, 2008, 19 (04) :1540-1547
[6]   The Primary Cilium as a Complex Signaling Center [J].
Berbari, Nicolas F. ;
O'Connor, Amber K. ;
Haycraft, Courtney J. ;
Yoder, Bradley K. .
CURRENT BIOLOGY, 2009, 19 (13) :R526-R535
[7]   Functional genomics of the cilium, a sensory organelle [J].
Blacque, OE ;
Perens, EA ;
Boroevich, KA ;
Inglis, PN ;
Li, CM ;
Warner, A ;
Khattra, J ;
Holt, RA ;
Ou, GS ;
Mah, AK ;
McKay, SJ ;
Huang, P ;
Swoboda, P ;
Jones, SJM ;
Marra, MA ;
Baillie, DL ;
Moerman, DG ;
Shaham, S ;
Leroux, MR .
CURRENT BIOLOGY, 2005, 15 (10) :935-941
[8]   Flagellar motility is required for the viability of the bloodstream trypanosome [J].
Broadhead, R ;
Dawe, HR ;
Farr, H ;
Griffiths, S ;
Hart, SR ;
Portman, N ;
Shaw, MK ;
Ginger, ML ;
Gaskell, SJ ;
McKean, PG ;
Gull, K .
NATURE, 2006, 440 (7081) :224-227
[9]   The graded response to sonic hedgehog depends on cilia architecture [J].
Caspary, Tamara ;
Larkins, Christine E. ;
Anderson, Kathryn V. .
DEVELOPMENTAL CELL, 2007, 12 (05) :767-778
[10]   Mutations in Radial Spoke Head Protein Genes RSPH9 and RSPH4A Cause Primary Ciliary Dyskinesia with Central-Microtubular-Pair Abnormalities [J].
Castleman, Victoria H. ;
Romio, Leila ;
Chodhari, Rahul ;
Hirst, Robert A. ;
de Castro, Sandra C. P. ;
Parker, Keith A. ;
Ybot-Gonzalez, Patricia ;
Emes, Richard D. ;
Wilson, Stephen W. ;
Wallis, Colin ;
Johnson, Colin A. ;
Herrera, Rene J. ;
Rutman, Andrew ;
Dixon, Mellisa ;
Shoemark, Amelia ;
Bush, Andrew ;
Hogg, Claire ;
Gardiner, R. Mark ;
Reish, Orit ;
Greene, Nicholas D. E. ;
O'Callaghan, Christopher ;
Purton, Saul ;
Chung, Eddie M. K. ;
Mitchison, Hannah M. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2009, 84 (02) :197-209