Intraflagellar transport: A critical player in photoreceptor development and the pathogenesis of retinal degenerative diseases

被引:2
作者
Gupta, Mohona [1 ,2 ]
Pazour, Gregory J. [1 ,3 ]
机构
[1] Univ Massachusetts, Chan Med Sch, Program Mol Med, Worcester, MA USA
[2] Univ Massachusetts, Morningside Grad Sch Biol Sci, Chan Med Sch, Worcester, MA USA
[3] Univ Massachusetts, Program Mol Med, Chan Med Sch, Suite 213 Biotech 2,373 Plantat St, Worcester, MA 01605 USA
基金
美国国家卫生研究院;
关键词
cilia; ciliopathy; flagella; intraflagellar transport; outer segment; photoreceptor; retinal degeneration; BARDET-BIEDL-SYNDROME; ASPHYXIATING THORACIC DYSTROPHY; RECESSIVE RETINITIS-PIGMENTOSA; LEBER CONGENITAL AMAUROSIS; LIGHT-DRIVEN TRANSLOCATION; PROTEIN-COUPLED RECEPTORS; OUTER SEGMENT; SENIOR-LOKEN; HYPOMORPHIC MUTATIONS; SKELETAL CILIOPATHIES;
D O I
10.1002/cm.21823
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In vertebrate vision, photons are detected by highly specialized sensory cilia called outer segments. Photoreceptor outer segments form by remodeling the membrane of a primary cilium into a stack of flattened disks. Intraflagellar transport (IFT) is critical to the formation of most types of eukaryotic cilia including the outer segments. This review covers the state of knowledge of the role of IFT in the formation and maintenance of outer segments and the human diseases that result from mutations in genes encoding the IFT complex and associated motors.
引用
收藏
页码:556 / 568
页数:13
相关论文
共 119 条
  • [1] Senior-Loken Syndrome with Rare Manifestations: A Case Report
    Aggarwal, Harikrishan K.
    Jain, Deepak
    Yadav, Sachin
    Kaverappa, Vipin
    Gupta, Abhishek
    [J]. EURASIAN JOURNAL OF MEDICINE, 2013, 45 (02) : 128 - 131
  • [2] ODA16p, a Chlamydomonas flagellar protein needed for dynein assembly
    Ahmed, NT
    Mitchell, DR
    [J]. MOLECULAR BIOLOGY OF THE CELL, 2005, 16 (10) : 5004 - 5012
  • [3] IFT27, encoding a small GTPase component of IFT particles, is mutated in a consanguineous family with Bardet-Biedl syndrome
    Aldahmesh, Mohammed A.
    Li, Yuanyuan
    Alhashem, Amal
    Anazi, Shams
    Alkuraya, Hisham
    Hashem, Mais
    Awaji, Ali A.
    Sogaty, Sameera
    Alkharashi, Abdullah
    Alzahrani, Saeed
    Al Hazzaa, Selwa A.
    Xiong, Yong
    Kong, Shanshan
    Sun, Zhaoxia
    Alkuraya, Fowzan S.
    [J]. HUMAN MOLECULAR GENETICS, 2014, 23 (12) : 3307 - 3315
  • [4] Avila-Fernández A, 2010, MOL VIS, V16, P2550
  • [5] Bardet-Biedl syndrome proteins are required for the localization of G protein-coupled receptors to primary cilia
    Berbari, Nicolas F.
    Lewis, Jacqueline S.
    Bishop, Georgia A.
    Askwith, Candice C.
    Mykytyn, Kirk
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (11) : 4242 - 4246
  • [6] NATURAL COURSE OF RETINITIS PIGMENTOSA OVER A 3-YEAR INTERVAL
    BERSON, EL
    SANDBERG, MA
    ROSNER, B
    BIRCH, DG
    HANSON, AH
    [J]. AMERICAN JOURNAL OF OPHTHALMOLOGY, 1985, 99 (03) : 240 - 251
  • [8] BERSON EL, 1993, INVEST OPHTH VIS SCI, V34, P1659
  • [9] Besharse JC., 1990, CILIARY FLAGELLUAR M, P389
  • [10] Molecular Basis of Tubulin Transport Within the Cilium by IFT74 and IFT81
    Bhogaraju, Sagar
    Cajanek, Lukas
    Fort, Cecile
    Blisnick, Thierry
    Weber, Kristina
    Taschner, Michael
    Mizuno, Naoko
    Lamla, Stefan
    Bastin, Philippe
    Nigg, Erich A.
    Lorentzen, Esben
    [J]. SCIENCE, 2013, 341 (6149) : 1009 - 1012