The base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalization

被引:349
作者
Reiter, Jeremy F. [3 ]
Blacque, Oliver E. [2 ]
Leroux, Michel R. [1 ]
机构
[1] Simon Fraser Univ, Dept Mol Biol & Biochem, Burnaby, BC V5A 1S6, Canada
[2] Univ Coll Dublin, UCD Conway Inst, Sch Biomol & Biomed Sci, Belfield, Ireland
[3] Univ Calif San Francisco, Cardiovasc Res Inst, Dept Biochem & Biophys, San Francisco, CA 94158 USA
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
cilium; transition zone; transition fibre; basal body; ciliopathy; OUTER SEGMENT FORMATION; MECKEL-GRUBER-SYNDROME; INTRAFLAGELLAR TRANSPORT; JOUBERT-SYNDROME; RETINAL DEGENERATION; DIFFUSION BARRIER; PLASMA-MEMBRANE; SOLUBLE-PROTEIN; FREEZE-FRACTURE; IMPORTIN-ALPHA;
D O I
10.1038/embor.2012.73
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Both the basal body and the microtubule-based axoneme it nucleates have evolutionarily conserved subdomains crucial for cilium bio-genesis, function and maintenance. Here, we focus on two conspicuous but underappreciated regions of these structures that make membrane connections. One is the basal body distal end, which includes transition fibres of largely undefined composition that link to the base of the ciliary membrane. Transition fibres seem to serve as docking sites for intraflagellar transport particles, which move proteins within the ciliary compartment and are required for cilium biogenesis and sustained function. The other is the proximal-most region of the axoneme, termed the transition zone, which is characterized by Y-shaped linkers that span from the axoneme to the ciliary necklace on the membrane surface. The transition zone comprises a growing number of ciliopathy proteins that function as modular components-of a ciliary gate. This gate, which forms early during ciliogenesis, might function in part by regulating intraflagellar transport. Together with a recently described septin ring diffusion barrier at the ciliary base, the transition fibres and transition zone deserve attention for their varied roles in forming functional ciliary compartments.
引用
收藏
页码:608 / 618
页数:11
相关论文
共 108 条
  • [92] SOROKIN SP, 1968, J CELL SCI, V3, P207
  • [93] SPENCER M, 1988, INVEST OPHTH VIS SCI, V29, P1012
  • [94] Epithelial polarity requires septin coupling of vesicle transport to polyglutamylated microtubules
    Spiliotis, Elias T.
    Hunt, Stephen J.
    Hu, Qicong
    Kinoshita, Makoto
    Nelson, W. James
    [J]. JOURNAL OF CELL BIOLOGY, 2008, 180 (02) : 295 - 303
  • [95] An essential quality control mechanism at the eukaryotic basal body prior to intraflagellar transport
    Stephan, Angela
    Vaughan, Sue
    Shaw, Michael K.
    Gull, Keith
    McKean, Paul G.
    [J]. TRAFFIC, 2007, 8 (10) : 1323 - 1330
  • [96] Plasma membrane compartmentalization in yeast by messenger RNA transport and a septin diffusion barrier
    Takizawa, PA
    DeRisi, JL
    Wilhelm, JE
    Vale, RD
    [J]. SCIENCE, 2000, 290 (5490) : 341 - 344
  • [97] The stumpy gene is required for mammalian ciliogenesis
    Town, Terrence
    Breunig, Joshua J.
    Sarkisian, Matthew R.
    Spilianakis, Charalampos
    Ayoub, Albert E.
    Liu, Xiuxin
    Ferrandino, Anthony F.
    Gallagher, A. Rachel
    Li, Ming O.
    Rakic, Pasko
    Flavell, Richard A.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (08) : 2853 - 2858
  • [98] Flagellar membrane localization via association with lipid rafts
    Tyler, Kevin M.
    Fridberg, Alina
    Toriello, Krista M.
    Olson, Cheryl L.
    Cieslak, John A.
    Hazlett, Theodore L.
    Engman, David M.
    [J]. JOURNAL OF CELL SCIENCE, 2009, 122 (06) : 859 - 866
  • [99] Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes
    Valente, Enza Maria
    Logan, Clare V.
    Mougou-Zerelli, Soumaya
    Lee, Jeong Ho
    Silhavy, Jennifer L.
    Brancati, Francesco
    Iannicelli, Miriam
    Travaglini, Lorena
    Romani, Sveva
    Illi, Barbara
    Adams, Matthew
    Szymanska, Katarzyna
    Mazzotta, Annalisa
    Lee, Ji Eun
    Tolentino, Jerlyn C.
    Swistun, Dominika
    Salpietro, Carmelo D.
    Fede, Carmelo
    Gabriel, Stacey
    Russ, Carsten
    Cibulskis, Kristian
    Sougnez, Carrie
    Hildebrandt, Friedhelm
    Otto, Edgar A.
    Held, Susanne
    Diplas, Bill H.
    Davis, Erica E.
    Mikula, Mario
    Strom, Charles M.
    Ben-Zeev, Bruria
    Lev, Dorit
    Sagie, Tally Lerman
    Michelson, Marina
    Yaron, Yuval
    Krause, Amanda
    Boltshauser, Eugen
    Elkhartoufi, Nadia
    Roume, Joelle
    Shalev, Stavit
    Munnich, Arnold
    Saunier, Sophie
    Inglehearn, Chris
    Saad, Ali
    Alkindy, Adila
    Thomas, Sophie
    Vekemans, Michel
    Dallapiccola, Bruno
    Katsanis, Nicholas
    Johnson, Colin A.
    Attie-Bitach, Tania
    [J]. NATURE GENETICS, 2010, 42 (07) : 619 - U100
  • [100] Ftm is a novel basal body protein of cilia involved in Shh signalling
    Vierkotten, Jeanette
    Dildrop, Renate
    Peters, Thomas
    Wang, Baolin
    Ruether, Ulrich
    [J]. DEVELOPMENT, 2007, 134 (14): : 2569 - 2577