Regulation of motor activity of ciliary outer-arm dynein by the light chain 1; Implications from the structure of the light chain bound to the microtubule-binding domain of the heavy chain-Reference-Cited by-同舟云学术

Regulation of motor activity of ciliary outer-arm dynein by the light chain 1; Implications from the structure of the light chain bound to the microtubule-binding domain of the heavy chain

Published:2023 Issue:1 Volume:20 Page:n/a
ISSN:2189-4779
Container-title:Biophysics and Physicobiology
language:en
Short-container-title:BIOPHYSICS

Author:

Yagi Toshiki¹^ORCID,Toda Akiyuki²,Ichikawa Muneyoshi³,Kurisu Genji²

Affiliation:

1. Faculty of Bioresource Sciences, Prefectural University of Hiroshima

2. Institute of Protein Research, Osaka University

3. State Key Laboratory of Genetic Engineering, Department of Biochemistry and Biophysics, School of Life Sciences, Fudan University

Publisher

Biophysical Society of Japan

Subject

Physiology,Molecular Biology,Biophysics,Biochemistry,Biochemistry, Genetics and Molecular Biology (miscellaneous)

Link

https://www.jstage.jst.go.jp/article/biophysico/20/1/20_e200008/_pdf

Reference43 articles.

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2. [2] Sanderson, M. J., Sleigh, M. A. Ciliary activity of cultured rabbit tracheal epithelium: beat pattern and metachrony. J Cell Sci. 47, 331–347 (1981). https://doi.org/10.1242/jcs.47.1.331

3. [3] Nonaka, S., Tanaka, Y., Okada, Y., Takeda, S., Harada, A., Kanai, Y., et al. Randomization of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein. Cell 95, 829–837 (1998). https://doi.org/10.1016/S0092-8674(00)81705-5

4. [4] Zariwala, M. A., Knowles, M. R., Omran, H. Genetic defects in ciliary structure and function. Annu. Rev. Physiol. 69, 423–450 (2007). https://doi.org/10.1146/annurev.physiol.69.040705.141301

5. [5] Reiter, J. F., Leroux, M. R. Genes and molecular pathways underpinning ciliopathies. Nat. Rev. Mol. Cell Biol. 9, 533–547 (2017). https://doi.org/10.1038/nrm.2017.60

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