|
|
|
||||
| Home Help Feedback Subscriptions Archive Search Table of Contents | |||||
Journal of Cell Science, Vol 112, Issue 11 1633-1644, Copyright © 1999 by Company of Biologists
JOURNAL ARTICLES |
KF Lechtreck, A Teltenkotter and A Grunow
Botanisches Institut, Universitat zu Koln, Gyrhofstr. 15, D-50931 Koln, Germany. kflecht@novell.biolan.uni-koeln.de
A monoclonal antibody raised against purified flagellar basal apparatuses from the green flagellate Spermatozopsis similis reacted with a protein of 210 kDa (p210) in western blots. The protein was partially cloned by immunoscreening of a cDNA library. The sequence encoded a novel protein rich in alanine (25%) and proline (20%), which contained regions similar to proteins of comparable amino acid composition such as extracellular matrix components or the membrane-cytoskeletal linker synapsin. Using a polyclonal antibody (anti-p210) raised against the C-terminal part of p210, it was shown that the protein was highly enriched in the basal apparatuses. Immunogold electron microscopy of isolated cytoskeletons or whole cells revealed that p210 was located in the flagellar transition region. The protein was part of the Y-shaped fibrous linkers between the doublet microtubules and the flagellar membrane, as indicated by statistical analysis of post-labeled sections using anti-centrin and anti-tubulin as controls. In premitotic cells p210 was located in a fibrous layer at the distal end of nascent basal bodies, which was perforated by the outgrowing axoneme. During deflagellation the protein remained at the basal body but we observed changes in its distribution, indicating that p210 partially moved to the tip of the basal body. p210 can be used as a marker to determine basal body position, orientation (parallel or antiparallel) and number in S. similis by indirect immunofluorescence. We suppose that p210 is involved in linking basal bodies to the plasma membrane, which is an important step during ciliogenesis.
This article has been cited by other articles:
![]() |
S. Geimer and M. Melkonian The ultrastructure of the Chlamydomonas reinhardtii basal apparatus: identification of an early marker of radial asymmetry inherent in the basal body J. Cell Sci., June 1, 2004; 117(13): 2663 - 2674. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. N. Gomperts, X. Gong-Cooper, and B. P. Hackett Foxj1 regulates basal body anchoring to the cytoskeleton of ciliated pulmonary epithelial cells J. Cell Sci., March 15, 2004; 117(8): 1329 - 1337. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. T. O'Toole, T. H. Giddings, J. R. McIntosh, and S. K. Dutcher Three-dimensional Organization of Basal Bodies from Wild-Type and {delta}-Tubulin Deletion Strains of Chlamydomonas reinhardtii Mol. Biol. Cell, July 1, 2003; 14(7): 2999 - 3012. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. D. Silflow, M. LaVoie, L.-W. Tam, S. Tousey, M. Sanders, W.-c. Wu, M. Borodovsky, and P. A. Lefebvre The Vfl1 Protein in Chlamydomonas Localizes in a Rotationally Asymmetric Pattern at the Distal Ends of the Basal Bodies J. Cell Biol., March 26, 2001; 153(1): 63 - 74. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. M. Preble, T. H. Giddings , Jr., and S. K. Dutcher Extragenic Bypass Suppressors of Mutations in the Essential Gene BLD2 Promote Assembly of Basal Bodies With Abnormal Microtubules in Chlamydomonas reinhardtii Genetics, January 1, 2001; 157(1): 163 - 181. [Abstract] [Full Text] |
||||