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


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

doi: 10.1242/10.1242/jcs.00168


This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
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 Mikami, A.
Right arrow Articles by Vallee, R. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Mikami, A.
Right arrow Articles by Vallee, R. B.
Journal of Cell Science 115, 4801-4808 (2002)
doi: 10.1242/jcs.00168


Research Article

Molecular structure of cytoplasmic dynein 2 and its distribution in neuronal and ciliated cells

Atsushi Mikami1, Sharon H. Tynan1, Taro Hama2, Katherine Luby-Phelps3, Tetsuichiro Saito2, James E. Crandall4, Joseph C. Besharse3 and Richard B. Vallee1,*

1 Department of Pathology, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA
2 Department of Development and Differentiation, Institute for Frontier Medical Sciences, Kyoto University, Kyoto 606-8507 Japan
3 Department of Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, WI 53226, USA
4 Department of Developmental Neurobiology, Eunice Kennedy Shriver Center, University of Massachusetts Medical School, Waltham, MA 02452, USA

* Author for correspondence (e-mail: rv2025{at}columbia.edu)

Accepted 12 September 2002

Cytoplasmic dynein is involved in a wide variety of cellular functions. In addition to the initially characterized form (MAP 1C/dynein 1), a second form of cytoplasmic dynein (dynein 2) has been identified and implicated in intraflagellar transport (IFT) in lower eukaryotes and in Golgi organization in vertebrates. In the current study, the primary structure of the full-length dynein 2 heavy chain (HC) was determined from cDNA sequence. The dynein 1 and dynein 2 sequences were similar within the motor region, and around the light intermediate chain (LIC)-binding site within the N-terminal stem region. The dynein 2 HC co-immunoprecipitated with LIC3, a homologue of dynein 1 LICs. Dynein 2 mRNA was abundant in the ependymal layer of the neural tube and in the olfactory epithelium. Antibodies to dynein 2 HC, LIC3 and a component of IFT particles strongly stained the ependymal layer lining the lateral ventricles. Both dynein 2 HC and LIC3 staining was also observed associated with connecting cilia in the retina and within primary cilia of non-neuronal cultured cells. These data support a specific role for dynein 2 in the generation and maintenance of cilia.

Key words: Dynein, Cilium, Microtubule, Retina, Light intermediate chain, Brain




This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
S. A. Baker, K. Freeman, K. Luby-Phelps, G. J. Pazour, and J. C. Besharse
IFT20 Links Kinesin II with a Mammalian Intraflagellar Transport Complex That Is Conserved in Motile Flagella and Sensory Cilia
J. Biol. Chem., September 5, 2003; 278(36): 34211 - 34218.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 2002