The roles of cilia in developmental disorders and disease

被引:257
作者
Bisgrove, Brent W. [1 ]
Yost, H. Joseph [1 ]
机构
[1] Univ Utah, Huntsman Canc Inst, Ctr Children, Dept Oncol Sci, Salt Lake City, UT 84112 USA
来源
DEVELOPMENT | 2006年 / 133卷 / 21期
关键词
D O I
10.1242/dev.02595
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cilia are highly conserved organelles that have diverse motility and sensory functions. Recent discoveries have revealed that cilia also have crucial roles in cell signaling pathways and in maintaining cellular homeostasis. As such, defects in cilia formation or function have profound effects on the development of body pattern and the physiology of multiple organ systems. By categorizing syndromes that are due to cilia dysfunction in humans and from studies in vertebrate model organisms, molecular pathways that intersect with cilia formation and function have come to light. Here, we summarize an emerging view that in order to understand some complex developmental pathways and disease etiologies, one must consider the molecular functions performed by cilia.
引用
收藏
页码:4131 / 4143
页数:13
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共 150 条
[1]  
AFZELIUS B A, 1976, Science (Washington D C), V193, P317
[2]   Cilia-related diseases [J].
Afzelius, BA .
JOURNAL OF PATHOLOGY, 2004, 204 (04) :470-477
[3]   Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome [J].
Ansley, SJ ;
Badano, JL ;
Blacque, OE ;
Hill, J ;
Hoskins, BE ;
Leitch, CC ;
Kim, JC ;
Ross, AJ ;
Eichers, ER ;
Teslovich, TM ;
Mah, AK ;
Johnsen, RC ;
Cavender, JC ;
Lewis, RA ;
Leroux, MR ;
Beales, PL ;
Katsanis, N .
NATURE, 2003, 425 (6958) :628-633
[4]   Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2 [J].
Badano, JL ;
Ansley, SJ ;
Leitch, CC ;
Lewis, RA ;
Lupski, JR ;
Katsanis, N .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (03) :650-658
[5]   Dysfunctional cilia lead to altered ependyma and choroid plexus function, and result in the formation of hydrocephalus [J].
Banizs, B ;
Pike, MM ;
Millican, CL ;
Ferguson, WB ;
Komlosi, P ;
Sheetz, J ;
Bell, PD ;
Schwiebert, EM ;
Yoder, BK .
DEVELOPMENT, 2005, 132 (23) :5329-5339
[6]   A polycystic kidney-disease gene homologue required for male mating behaviour in C-elegans [J].
Barr, MM ;
Sternberg, PW .
NATURE, 1999, 401 (6751) :386-389
[7]   The Caenorhabditis elegans autosomal dominant polycystic kidney disease gene homologs lov-1 and pkd-2 act in the same pathway [J].
Barr, MM ;
DeModena, J ;
Braun, D ;
Nguyen, CQ ;
Hall, DH ;
Sternberg, PW .
CURRENT BIOLOGY, 2001, 11 (17) :1341-1346
[8]   Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia [J].
Bartoloni, L ;
Blouin, JL ;
Pan, YZ ;
Gehrig, C ;
Maiti, AK ;
Scamuffa, N ;
Rossier, C ;
Jorissen, M ;
Armengot, M ;
Meeks, M ;
Mitchison, HM ;
Chung, EMK ;
Delozier-Blanchet, CD ;
Craigen, WJ ;
Antonarakis, SE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (16) :10282-10286
[9]   Polaris and Polycystin-2 in dorsal forerunner cells and Kupffer's vesicle are required for specification of the zebrafish left-right axis [J].
Bisgrove, BW ;
Snarr, BS ;
Emrazian, A ;
Yost, HJ .
DEVELOPMENTAL BIOLOGY, 2005, 287 (02) :274-288
[10]   Loss of C-elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport [J].
Blacque, OE ;
Reardon, MJ ;
Li, CM ;
McCarthy, J ;
Mahjoub, MR ;
Ansley, SJ ;
Badano, LL ;
Mah, AK ;
Beales, PL ;
Davidson, WS ;
Johnsen, RC ;
Audeh, M ;
Plasterk, RHA ;
Baillie, DL ;
Katsanis, N ;
Quarmby, LM ;
Wicks, SR ;
Leroux, MR .
GENES & DEVELOPMENT, 2004, 18 (13) :1630-1642