@article{5956a6e26ae04dabb4102630c8ad4617,
title = "Cell type-specific structural plasticity of the ciliary transition zone in C. elegans",
abstract = "Background information: The current consensus on cilia development posits that the ciliary transition zone (TZ) is formed via extension of nine centrosomal microtubules. In this model, TZ structure remains unchanged in microtubule number throughout the cilium life cycle. This model does not however explain structural variations of TZ structure seen in nature and could also lend itself to the misinterpretation that deviations from nine-doublet microtubule ultrastructure represent an abnormal phenotype. Thus, a better understanding of events that occur at the TZ in vivo during metazoan development is required. Results: To address this issue, we characterized ultrastructure of two types of sensory cilia in developing Caenorhabditis elegans. We discovered that, in cephalic male (CEM) and inner labial quadrant (IL2Q) sensory neurons, ciliary TZs are structurally plastic and remodel from one structure to another during animal development. The number of microtubule doublets forming the TZ can be increased or decreased over time, depending on cilia type. Both cases result in structural TZ intermediates different from TZ in cilia of adult animals. In CEM cilia, axonemal extension and maturation occurs concurrently with TZ structural maturation. Conclusions and Significance: Our work extends the current model to include the structural plasticity of metazoan transition zone, which can be structurally delayed, maintained or remodelled in cell type-specific manner.",
keywords = "C. elegans, axoneme, cilia, microtubule, transition zone",
author = "Akella, {Jyothi S.} and Malan Silva and Morsci, {Natalia S.} and Nguyen, {Ken C.} and Rice, {William J.} and Hall, {David H.} and Barr, {Maureen M.}",
note = "Funding Information: This work was funded by National Institutes of Health grants DK059418 and DK116606 (to M. M. B.), OD 010943 (to D. H. H), postdoctoral fellowship from the New Jersey Commission on Spinal Cord Research CSCR16FEL008 (to J. S. A.), personal savings (of N. S. M.), and Waksman Institute Charles and Johanna Busch Fellowship and University Bevier Fellowship (to M. S.). Some of this work was performed at the Simons Electron Microscopy Center and National Resource for Automated Molecular Microscopy located at the New York Structural Biology Center, supported by grants from the Simons Foundation (SF349247), NYSTAR and the NIH National Institute of General Medical Sciences (GM103310), with additional support from Agouron Institute (F00316) and NIH (OD019994 and RR029300). Some strains were provided by the National BioResource Project and the Caenorhabditis Genetics Center (CGC), which is funded by NIH Office of Research Infrastructure Programs [P40 OD010440]. Authors declare no competing financial interests or any funding that can compromise the integrity of this work. We thank Leslie Gunther and Frank Macaluso for help in HPF-FS performed at Albert Einstein College of Medicine, Ed Eng at the New York Structural Biology Center (NYSBC) for help in electron tomography, Gloria Androwski for on-going outstanding laboratory support, WormBase and WormAtlas for online resources, the Barr lab for discussion and constructive criticisms, Joel Rosenbaum for feedback on the manuscript. We also thank Dr. Jeff W. Barclay at the University of Liverpool, UK, for generously sharing unpublished data about IL2 neurons. Funding Information: This work was funded by National Institutes of Health grants DK059418 and DK116606 (to M. M. B.), OD 010943 (to D. H. H), postdoctoral fellowship from the New Jersey Commission on Spinal Cord Research CSCR16FEL008 (to J. S. A.), personal savings (of N. S. M.), and Waksman Institute Charles and Johanna Busch Fellowship and University Bevier Fellowship (to M. S.). Some of this work was performed at the Simons Electron Microscopy Center and National Resource for Automated Molecular Microscopy located at the New York Structural Biology Center, supported by grants from the Simons Foundation (SF349247), NYSTAR and the NIH National Institute of General Medical Sciences (GM103310), with additional support from Agouron Institute (F00316) and NIH (OD019994 and RR029300). Some strains were provided by the National BioResource Project and the Caenorhabditis Genetics Center (CGC), which is funded by NIH Office of Research Infrastructure Programs [P40 OD010440]. Authors declare no competing financial interests or any funding that can compromise the integrity of this work. Publisher Copyright: {\textcopyright} 2019 Soci{\'e}t{\'e} Fran{\c c}aise des Microscopies and Soci{\'e}t{\'e} de Biologie Cellulaire de France. Published by John Wiley & Sons Ltd",
year = "2019",
month = apr,
doi = "10.1111/boc.201800042",
language = "English (US)",
volume = "111",
pages = "95--107",
journal = "Biology of the Cell",
issn = "0248-4900",
publisher = "Portland Press Ltd.",
number = "4",
}