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
  • [1] TERMINOLOGY AND NOMENCLATURE OF THE CYTOSKELETAL ELEMENTS ASSOCIATED WITH THE FLAGELLAR CILIARY APPARATUS IN PROTISTS
    ANDERSEN, RA
    BARR, DJS
    LYNN, DH
    MELKONIAN, M
    MOESTRUP, O
    SLEIGH, MA
    [J]. PROTOPLASMA, 1991, 164 (1-3) : 1 - 8
  • [2] 3-DIMENSIONAL STRUCTURE OF BASAL BODY FROM RHESUS-MONKEY OVIDUCT
    ANDERSON, RG
    [J]. JOURNAL OF CELL BIOLOGY, 1972, 54 (02) : 246 - &
  • [3] hPOC5 is a centrin-binding protein required for assembly of full-length centrioles
    Azimzadeh, Juliette
    Hergert, Polla
    Delouvee, Annie
    Euteneuer, Ursula
    Formstecher, Etienne
    Khodjakov, Alexey
    Bornens, Michel
    [J]. JOURNAL OF CELL BIOLOGY, 2009, 185 (01) : 101 - 114
  • [4] Making Sense of Cilia in Disease: The Human Cilloplathies
    Baker, Kate
    Beales, Philip L.
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2009, 151C (04) : 281 - 295
  • [5] Compartmentalization of the cell cortex by septins is required for maintenance of cell polarity in yeast
    Barral, Y
    Mermall, V
    Mooseker, MS
    Snyder, M
    [J]. MOLECULAR CELL, 2000, 5 (05) : 841 - 851
  • [6] Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteins
    Bialas, Nathan J.
    Inglis, Peter N.
    Li, Chunmei
    Robinson, Jon F.
    Parker, Jeremy D. K.
    Healey, Michael P.
    Davis, Erica E.
    Inglis, Chrystal D.
    Toivonen, Tiina
    Cottell, David C.
    Blacque, Oliver E.
    Quarmby, Lynne M.
    Katsanis, Nicholas
    Leroux, Michel R.
    [J]. JOURNAL OF CELL SCIENCE, 2009, 122 (05) : 611 - 624
  • [7] Functional genomics of the cilium, a sensory organelle
    Blacque, OE
    Perens, EA
    Boroevich, KA
    Inglis, PN
    Li, CM
    Warner, A
    Khattra, J
    Holt, RA
    Ou, GS
    Mah, AK
    McKay, SJ
    Huang, P
    Swoboda, P
    Jones, SJM
    Marra, MA
    Baillie, DL
    Moerman, DG
    Shaham, S
    Leroux, MR
    [J]. CURRENT BIOLOGY, 2005, 15 (10) : 935 - 941
  • [8] Intraflagellar transport: from molecular characterisation to mechanism
    Blacque, Oliver E.
    Cevik, Sebiha
    Kaplan, Oktay Ismail
    [J]. FRONTIERS IN BIOSCIENCE-LANDMARK, 2008, 13 : 2633 - 2652
  • [9] BOISVIEUXULRICH E, 1989, J CELL SCI, V92, P9
  • [10] Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice
    Boldt, Karsten
    Mans, Dorus A.
    Won, Jungyeon
    van Reeuwijk, Jeroen
    Vogt, Andreas
    Kinkl, Norbert
    Letteboer, Stef J. F.
    Hicks, Wanda L.
    Hurd, Ron E.
    Naggert, Jurgen K.
    Texier, Yves
    den Hollander, Anneke I.
    Koenekoop, Robert K.
    Bennett, Jean
    Cremers, Frans P. M.
    Gloeckner, Christian J.
    Nishina, Patsy M.
    Roepman, Ronald
    Ueffing, Marius
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2011, 121 (06) : 2169 - 2180