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
相关论文
共 150 条
[71]   Bend propagation drives central pair rotation in Chlamydomonas reinhardtii flagella [J].
Mitchell, DR ;
Nakatsugawa, M .
JOURNAL OF CELL BIOLOGY, 2004, 166 (05) :709-715
[72]   Cloning of inv, a gene that controls left/right asymmetry and kidney development [J].
Mochizuki, T ;
Saijoh, Y ;
Tsuchiya, K ;
Shirayoshi, Y ;
Takai, S ;
Taya, C ;
Yonekawa, H ;
Yamada, K ;
Nihei, H ;
Nakatsuji, N ;
Overbeek, PA ;
Hamada, H ;
Yokoyama, T .
NATURE, 1998, 395 (6698) :177-181
[73]   The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin [J].
Mollet, G ;
Salomon, R ;
Gribouval, O ;
Silbermann, F ;
Bacq, D ;
Landthaler, G ;
Milford, D ;
Nayir, A ;
Rizzoni, G ;
Antignac, C ;
Saunier, S .
NATURE GENETICS, 2002, 32 (02) :300-305
[74]   Expression analyses and interaction with the anaphase promoting complex protein Apc2 suggest a role for inversin in primary cilia and involvement in the cell cycle [J].
Morgan, D ;
Eley, L ;
Sayer, J ;
Strachan, T ;
Yates, LM ;
Craighead, AS ;
Goodship, JA .
HUMAN MOLECULAR GENETICS, 2002, 11 (26) :3345-3350
[75]   The left-right determinant inversin has highly conserved ankyrin repeat and IQ domains and interacts with calmodulin [J].
Morgan, D ;
Goodship, J ;
Essner, JJ ;
Vogan, KJ ;
Turnpenny, L ;
Yost, HJ ;
Tabin, CJ ;
Strachan, T .
HUMAN GENETICS, 2002, 110 (04) :377-384
[76]  
Murcia NS, 2000, DEVELOPMENT, V127, P2347
[77]   Bardet-Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assembly [J].
Mykytyn, K ;
Mullins, RF ;
Andrews, M ;
Chiang, AP ;
Swiderski, RE ;
Yang, BL ;
Braun, T ;
Casavant, T ;
Stone, EM ;
Sheffield, VC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (23) :8664-8669
[78]   Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome [J].
Mykytyn, K ;
Nishimura, DY ;
Searby, CC ;
Shastri, M ;
Yen, HJ ;
Beck, JS ;
Braun, T ;
Streb, LM ;
Cornier, AS ;
Cox, GF ;
Fulton, AB ;
Carmi, R ;
Lüleci, G ;
Chandrasekharappa, SC ;
Collins, FS ;
Jacobson, SG ;
Heckenlively, JR ;
Weleber, RG ;
Stone, EM ;
Sheffield, VC .
NATURE GENETICS, 2002, 31 (04) :435-438
[79]   Identification of the gene that, when mutated, causes the human obesity syndrome BBS4 [J].
Mykytyn, K ;
Braun, T ;
Carmi, R ;
Haider, NB ;
Searby, CC ;
Shastri, M ;
Beck, G ;
Wright, AF ;
Iannaccone, A ;
Elbedour, K ;
Riise, R ;
Baldi, A ;
Raas-Rothschild, A ;
Gorman, SW ;
Duhl, DM ;
Jacobson, SG ;
Casavant, T ;
Stone, EM ;
Sheffield, VC .
NATURE GENETICS, 2001, 28 (02) :188-191
[80]   Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells [J].
Nauli, SM ;
Alenghat, FJ ;
Luo, Y ;
Williams, E ;
Vassilev, P ;
Lil, XG ;
Elia, AEH ;
Lu, WN ;
Brown, EM ;
Quinn, SJ ;
Ingber, DE ;
Zhou, J .
NATURE GENETICS, 2003, 33 (02) :129-137