The fully linked HTML version of this article has now been published.
JCS ePress
online publication date 16 Jan 2007
doi: 10.1242/jcs.03352
Research Article
Functional genomics in Trypanosoma brucei identifies evolutionarily conserved components of motile flagella
Desiree M. Baron,
Katherine S. Ralston,
Zakayi P. Kabututu,
and
Kent L. Hill*
* Author for correspondence (e-mail: kenthill{at}mednet.ucla.edu)
Cilia and flagella are highly conserved, complex organelles involved in a variety of important functions. Flagella are required for motility of several human pathogens and ciliary defects lead to a variety of fatal and debilitating human diseases. Many of the major structural components of cilia and flagella are known, but little is known about regulation of flagellar beat. Trypanosoma brucei, the causative agent of African sleeping sickness, provides an excellent model for studying flagellar motility. We have used comparative genomics to identify a core group of 50 genes unique to organisms with motile flagella. These genes, referred to as T. brucei components of motile flagella (TbCMF) include 30 novel genes, and human homologues of many of the TbCMF genes map to loci associated with human ciliary diseases. To characterize TbCMF protein function we used RNA interference to target 41 TbCMF genes. Sedimentation assays and direct observation demonstrated clear motility defects in a majority of these knockdown mutants. Epitope tagging, fluorescence localization and biochemical fractionation demonstrated flagellar localization for several TbCMF proteins. Finally, ultrastructural analysis identified a family of novel TbCMF proteins that function to maintain connections between outer doublet microtubules, suggesting that they are the first identified components of nexin links. Overall, our results provide insights into the workings of the eukaryotic flagellum, identify several novel human disease gene candidates, reveal unique aspects of the trypanosome flagellum and underscore the value of T. brucei as an experimental system for studying flagellar biology.

CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati
Twitter What's this?
This article has been cited by other articles:

|
 |

|
 |
 
J. A. Rodriguez, M. A. Lopez, M. C. Thayer, Y. Zhao, M. Oberholzer, D. D. Chang, N. K. Kisalu, M. L. Penichet, G. Helguera, R. Bruinsma, et al.
Propulsion of African trypanosomes is driven by bihelical waves with alternating chirality separated by kinks
PNAS,
November 17, 2009;
106(46):
19322 - 19327.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. Adhiambo, T. Blisnick, G. Toutirais, E. Delannoy, and P. Bastin
A novel function for the atypical small G protein Rab-like 5 in the assembly of the trypanosome flagellum
J. Cell Sci.,
March 15, 2009;
122(6):
834 - 841.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. Kubo, A. Yuba-Kubo, S. Tsukita, S. Tsukita, and M. Amagai
Sentan: A Novel Specific Component of the Apical Structure of Vertebrate Motile Cilia
Mol. Biol. Cell,
December 1, 2008;
19(12):
5338 - 5346.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. Absalon, T. Blisnick, L. Kohl, G. Toutirais, G. Dore, D. Julkowska, A. Tavenet, and P. Bastin
Intraflagellar Transport and Functional Analysis of Genes Required for Flagellum Formation in Trypanosomes
Mol. Biol. Cell,
March 1, 2008;
19(3):
929 - 944.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
P. Rompolas, L. B. Pedersen, R. S. Patel-King, and S. M. King
Chlamydomonas FAP133 is a dynein intermediate chain associated with the retrograde intraflagellar transport motor
J. Cell Sci.,
October 15, 2007;
120(20):
3653 - 3665.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. M. Baron, Z. P. Kabututu, and K. L. Hill
Stuck in reverse: loss of LC1 in Trypanosoma brucei disrupts outer dynein arms and leads to reverse flagellar beat and backward movement
J. Cell Sci.,
May 1, 2007;
120(9):
1513 - 1520.
[Abstract]
[Full Text]
[PDF]
|
 |
|
© The Company of Biologists Ltd 2007