6533b881fe1ef96bd12d85e4

RESEARCH PRODUCT

Additional file 4: of KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome

Anna SandersErik De VriezeAnas AlazamiFatema AlzahraniErik MalarkeyNasrin SoruschLars TebbeStefanie KuhnsTeunis Van DamAmal AlhashemBrahim TabarkiQianhao LuNils LambacherJulie KennedyRachel BowieLisette HetterschijtSylvia Van BeersumJeroen Van ReeuwijkKarsten BoldtHannie KremerRobert KestersonDorota MoniesMohamed AbouelhodaRonald RoepmanMartijn HuynenMarius UeffingRob RussellUwe WolfrumBradley YoderErwin Van WijkFowzan AlkurayaOliver Blacque

subject

description

IFT analysis in C. elegans K04F10.2( tm1830 ) mutants. a Intraflagellar transport rates in wild-type and K04F10.2(tm1830) mutant worms. Shown are the anterograde and retrograde velocities (μm.s-1/standard deviation (SD)) of GFP-tagged IFT proteins along amphid and phasmid channel cilia (combined; top rows), or phasmid cilia only (bottom rows). t-test pairwise comparison with wild-type controls, n number of particles, N measured number of amphids and phasmids. OSM-3 is the worm orthologue of KIF17; CHE-11 is the worm orthologue of IFT140; OSM-6 is the worm orthologue of IFT52. b Representative fluorescence images of phasmid cilia showing normal IFT protein localisations and distributions in tm1830 mutants. ds distal segment, ms middle segment, bb basal body region, den dendrite. All images are similarly scaled and orientated (arrow denotes basal body). Scale bar, 3 μm. c Representative kymographs (time (t) over distance (d) plots) used to generate IFT rate measurements. For each kymograph, the horizontal axis (distance) is 5 μm and the vertical axis (time) is 25 seconds. d Distribution plots of IFT protein velocities. (JPG 1951 kb)

https://dx.doi.org/10.6084/m9.figshare.c.3613589_d4.v1