spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search    

The fully linked HTML version of this article has now been published.
Development ePress online publication date 6 Jun 2007
doi: 10.1242/dev.003715


This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
dev.003715v1
134/14/2569    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Vierkotten, J.
Right arrow Articles by Rüther, U.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Vierkotten, J.
Right arrow Articles by Rüther, U.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Research article

Ftm is a novel basal body protein of cilia involved in Shh signalling


Jeanette Vierkotten, Renate Dildrop, Thomas Peters, Baolin Wang, and Ulrich Rüther*
* Author for correspondence (e-mail: ruether{at}uni-duesseldorf.de)

In this study we show in mice that Ftm (Rpgrip1l) is located at the ciliary basal body. Our data reveal that Ftm is necessary for developmental processes such as the establishment of left-right asymmetry and patterning of the neural tube and the limbs. The loss of Ftm affects the ratio of Gli3 activator to Gli3 repressor, suggesting an involvement of Ftm in Shh signalling. As Ftm is not essential for cilia assembly but for full Shh response, Ftm can be considered as a novel component for cilium-related Hh signalling. Furthermore, the absence of Ftm in arthropods underlines the divergence between vertebrate and Drosophila Hh pathways.


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
Hum Mol GenetHome page
S. D. Weatherbee, L. A. Niswander, and K. V. Anderson
A mouse model for Meckel syndrome reveals Mks1 is required for ciliogenesis and Hedgehog signaling
Hum. Mol. Genet., December 1, 2009; 18(23): 4565 - 4575.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
Y.-C. Hsiao, Z. J. Tong, J. E. Westfall, J. G. Ault, P. S. Page-McCaw, and R. J. Ferland
Ahi1, whose human ortholog is mutated in Joubert syndrome, is required for Rab8a localization, ciliogenesis and vesicle trafficking
Hum. Mol. Genet., October 15, 2009; 18(20): 3926 - 3941.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
P. Huang and A. F. Schier
Dampened Hedgehog signaling but normal Wnt signaling in zebrafish without cilia
Development, September 15, 2009; 136(18): 3089 - 3098.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
V. L. Patterson, C. Damrau, A. Paudyal, B. Reeve, D. T. Grimes, M. E. Stewart, D. J. Williams, P. Siggers, A. Greenfield, and J. N. Murdoch
Mouse hitchhiker mutants have spina bifida, dorso-ventral patterning defects and polydactyly: identification of Tulp3 as a novel negative regulator of the Sonic hedgehog pathway
Hum. Mol. Genet., May 15, 2009; 18(10): 1719 - 1739.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
N. J. Bialas, P. N. Inglis, C. Li, J. F. Robinson, J. D. K. Parker, M. P. Healey, E. E. Davis, C. D. Inglis, T. Toivonen, D. C. Cottell, et al.
Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteins
J. Cell Sci., March 1, 2009; 122(5): 611 - 624.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
Y. Yin, F. Bangs, I. R. Paton, A. Prescott, J. James, M. G. Davey, P. Whitley, G. Genikhovich, U. Technau, D. W. Burt, et al.
The Talpid3 gene (KIAA0586) encodes a centrosomal protein that is essential for primary cilia formation
Development, February 15, 2009; 136(4): 655 - 664.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
M. Varjosalo and J. Taipale
Hedgehog: functions and mechanisms
Genes & Dev., September 15, 2008; 22(18): 2454 - 2472.
[Abstract] [Full Text] [PDF]


Home page
Nephrol Dial TransplantHome page
O. Devuyst and V. J. Arnould
Mutations in RPGRIP1L: extending the clinical spectrum of ciliopathies
Nephrol. Dial. Transplant., May 1, 2008; 23(5): 1500 - 1503.
[Full Text] [PDF]


Home page
J. Med. Genet.Home page
M Adams, U M Smith, C V Logan, and C A Johnson
Recent advances in the molecular pathology, cell biology and genetics of ciliopathies
J. Med. Genet., May 1, 2008; 45(5): 257 - 267.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
G. Stratigopoulos, S. L. Padilla, C. A. LeDuc, E. Watson, A. T. Hattersley, M. I. McCarthy, L. M. Zeltser, W. K. Chung, and R. L. Leibel
Regulation of Fto/Ftm gene expression in mice and humans
Am J Physiol Regulatory Integrative Comp Physiol, April 1, 2008; 294(4): R1185 - R1196.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 2007