Microtubule asters anchored by FSD1 control axoneme assembly and ciliogenesis
Hai-Qing Tu,
Xuan-He Qin,
Zhi-Bin Liu,
Zeng-Qing Song,
Huai-Bin Hu,
Yu-Cheng Zhang,
Yan Chang,
Min Wu,
Yan Huang,
Yun-Feng Bai,
Guang Wang,
Qiu-Ying Han,
Ai-Ling Li,
Tao Zhou,
Feng Liu (),
Xue-Min Zhang () and
Hui-Yan Li ()
Additional contact information
Hai-Qing Tu: National Center of Biomedical Analysis
Xuan-He Qin: National Center of Biomedical Analysis
Zhi-Bin Liu: University of Chinese Academy of Science
Zeng-Qing Song: National Center of Biomedical Analysis
Huai-Bin Hu: National Center of Biomedical Analysis
Yu-Cheng Zhang: National Center of Biomedical Analysis
Yan Chang: National Center of Biomedical Analysis
Min Wu: National Center of Biomedical Analysis
Yan Huang: National Center of Biomedical Analysis
Yun-Feng Bai: National Center of Biomedical Analysis
Guang Wang: National Center of Biomedical Analysis
Qiu-Ying Han: National Center of Biomedical Analysis
Ai-Ling Li: National Center of Biomedical Analysis
Tao Zhou: National Center of Biomedical Analysis
Feng Liu: Chinese Academy of Sciences
Xue-Min Zhang: National Center of Biomedical Analysis
Hui-Yan Li: National Center of Biomedical Analysis
Nature Communications, 2018, vol. 9, issue 1, 1-17
Abstract:
Abstract Defective ciliogenesis causes human developmental diseases termed ciliopathies. Microtubule (MT) asters originating from centrosomes in mitosis ensure the fidelity of cell division by positioning the spindle apparatus. However, the function of microtubule asters in interphase remains largely unknown. Here, we reveal an essential role of MT asters in transition zone (TZ) assembly during ciliogenesis. We demonstrate that the centrosome protein FSD1, whose biological function is largely unknown, anchors MT asters to interphase centrosomes by binding to microtubules. FSD1 knockdown causes defective ciliogenesis and affects embryonic development in vertebrates. We further show that disruption of MT aster anchorage by depleting FSD1 or other known anchoring proteins delocalizes the TZ assembly factor Cep290 from centriolar satellites, and causes TZ assembly defects. Thus, our study establishes FSD1 as a MT aster anchorage protein and reveals an important function of MT asters anchored by FSD1 in TZ assembly during ciliogenesis.
Date: 2018
References: Add references at CitEc
Citations:
Downloads: (external link)
https://www.nature.com/articles/s41467-018-07664-2 Abstract (text/html)
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-07664-2
Ordering information: This journal article can be ordered from
https://www.nature.com/ncomms/
DOI: 10.1038/s41467-018-07664-2
Access Statistics for this article
Nature Communications is currently edited by Nathalie Le Bot, Enda Bergin and Fiona Gillespie
More articles in Nature Communications from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().