{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T23:05:58Z","timestamp":1791327958687,"version":"4.3.1"},"reference-count":69,"publisher":"American Society for Cell Biology (ASCB)","issue":"19","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["MBoC"],"published-print":{"date-parts":[[2014,10]]},"abstract":"<jats:p>Defects in centrosome and cilium function are associated with phenotypically related syndromes called ciliopathies. Cby1, the mammalian orthologue of the Drosophila Chibby protein, localizes to mature centrioles, is important for ciliogenesis in multiciliated airway epithelia in mice, and antagonizes canonical Wnt signaling via direct regulation of \u03b2-catenin. We report that deletion of the mouse Cby1 gene results in cystic kidneys, a phenotype common to ciliopathies, and that Cby1 facilitates the formation of primary cilia and ciliary recruitment of the Joubert syndrome protein Arl13b. Localization of Cby1 to the distal end of mature centrioles depends on the centriole protein Ofd1. Superresolution microscopy using both three-dimensional SIM and STED reveals that Cby1 localizes to an \u223c250-nm ring at the distal end of the mature centriole, in close proximity to Ofd1 and Ahi1, a component of the transition zone between centriole and cilium. The amount of centriole-localized Ahi1, but not Ofd1, is reduced in Cby1<jats:sup>\u2212\/\u2212<\/jats:sup>cells. This suggests that Cby1 is required for efficient recruitment of Ahi1, providing a possible molecular mechanism for the ciliogenesis defect in Cby1<jats:sup>\u2212\/\u2212<\/jats:sup>cells.<\/jats:p>","DOI":"10.1091\/mbc.e14-02-0735","type":"journal-article","created":{"date-parts":[[2014,8,8]],"date-time":"2014-08-08T02:54:50Z","timestamp":1407466490000},"page":"2919-2933","source":"Crossref","is-referenced-by-count":65,"title":["Cby1 promotes Ahi1 recruitment to a ring-shaped domain at the centriole\u2013cilium interface and facilitates proper cilium formation and function"],"prefix":"10.1091","volume":"25","author":[{"given":"Yin Loon","family":"Lee","sequence":"first","affiliation":[{"name":"Department of Biology, Stanford School of Medicine, Stanford University, Stanford, CA 94305"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Joshua","family":"Sant\u00e9","sequence":"additional","affiliation":[{"name":"Department of Biology, Stanford School of Medicine, Stanford University, Stanford, CA 94305"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Colin J.","family":"Comerci","sequence":"additional","affiliation":[{"name":"Department of Chemistry, Stanford School of Medicine, Stanford University, Stanford, CA 94305"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Benjamin","family":"Cyge","sequence":"additional","affiliation":[{"name":"Department of Pharmacological Sciences, Stony Brook University, Stony Brook, NY 11794"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Luis F.","family":"Menezes","sequence":"additional","affiliation":[{"name":"National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Feng-Qian","family":"Li","sequence":"additional","affiliation":[{"name":"Department of Pharmacological Sciences, Stony Brook University, Stony Brook, NY 11794"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gregory G.","family":"Germino","sequence":"additional","affiliation":[{"name":"National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"W. 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