The Ciliary Rootlet Maintains Long-Term Stability of Sensory Cilia

Author:

Yang Jun1,Gao Jiangang2,Adamian Michael1,Wen Xiao-Hong3,Pawlyk Basil1,Zhang Luo4,Sanderson Michael J.4,Zuo Jian2,Makino Clint L.3,Li Tiansen1

Affiliation:

1. The Berman-Gund Laboratory for the Study of Retinal Degenerations

2. Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, Tennessee

3. Howe Laboratory, Department of Ophthalmology, Harvard Medical School, Massachusetts Eye and Ear Infirmary, Boston, Massachusetts 02114

4. Department of Physiology, University of Massachusetts Medical School, Worcester, Massachusetts

Abstract

ABSTRACT The striated ciliary rootlet is a prominent cytoskeleton originating from basal bodies of ciliated cells. Although a familiar structure in cell biology, its function has remained unresolved. In this study, we carried out targeted disruption in mice of the gene for rootletin, a component of the rootlet. In the mutant, ciliated cells are devoid of rootlets. Phototransduction and ciliary beating in sensory and motile cilia initially exhibit no apparent functional deficits. However, photoreceptors degenerate over time, and mutant lungs appear prone to pathological changes consistent with insufficient mucociliary clearance. Further analyses revealed a striking fragility at the ciliary base in photoreceptors lacking rootlets. In vitro assays suggest that the rootlet is among the least dynamic of all cytoskeletons and interacts with actin filaments. Thus, a primary function of the rootlet is to provide structural support for the cilium. Inasmuch as photoreceptors elaborate an exceptionally enlarged sensory cilium, they are especially dependent on the rootlet for structural integrity and long-term survival.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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3. Besharse, J. C., and C. J. Horst. 1990. The photoreceptor connecting cilium: a model for the transition zone, p. 389-417. In R. A. Bloodgood (ed.), Ciliary and flagellar membranes. Plenum, New York, N.Y.

4. Fariss, R. N., R. S. Molday, S. K. Fisher, and B. Matsumoto. 1997. Evidence from normal and degenerating photoreceptors that two outer segment integral membrane proteins have separate transport pathways. J. Comp. Neurol. 387 : 148-156.

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