Detailed Information on Publication Record
2019
Fibroblast growth factor receptor influences primary cilium length through an interaction with intestinal cell kinase
BOSÁKOVÁ, Michaela, Alexandru NITĂ, Tomáš GREGOR, Miroslav VAŘECHA, Iva GUDERNOVÁ et. al.Basic information
Original name
Fibroblast growth factor receptor influences primary cilium length through an interaction with intestinal cell kinase
Authors
BOSÁKOVÁ, Michaela (203 Czech Republic, belonging to the institution), Alexandru NITĂ (642 Romania, belonging to the institution), Tomáš GREGOR (203 Czech Republic, belonging to the institution), Miroslav VAŘECHA (203 Czech Republic, belonging to the institution), Iva GUDERNOVÁ (203 Czech Republic, belonging to the institution), Bohumil FAFÍLEK (203 Czech Republic, belonging to the institution), Tomáš BÁRTA (203 Czech Republic, belonging to the institution), Neha BASHEER (356 India, belonging to the institution), Sara POOVAKULATHU ABRAHAM (356 India, belonging to the institution), Lukáš BÁLEK (203 Czech Republic, belonging to the institution), Markéta TOMANOVÁ (203 Czech Republic, belonging to the institution), Jana FIALOVÁ KUČEROVÁ (203 Czech Republic, belonging to the institution), Juraj BOSÁK (703 Slovakia, belonging to the institution), David POTĚŠIL (203 Czech Republic, belonging to the institution), Jennifer ZIEBA (840 United States of America), Jieun SONG (410 Republic of Korea), Peter KONIK (203 Czech Republic), Sohyun PARK (840 United States of America), Ivan DURAN (840 United States of America), Zbyněk ZDRÁHAL (203 Czech Republic, belonging to the institution), David ŠMAJS (203 Czech Republic, belonging to the institution), Gert JANSEN (528 Netherlands), Zheng FU (840 United States of America), Hyuk Wan KO (410 Republic of Korea), Aleš HAMPL (203 Czech Republic, belonging to the institution), Lukáš TRANTÍREK (203 Czech Republic, belonging to the institution), Deborah KRAKOW (840 United States of America) and Pavel KREJČÍ (203 Czech Republic, guarantor, belonging to the institution)
Edition
Proceedings of the National Academy of Sciences of the United States of America, WASHINGTON, NATL ACAD SCIENCES, 2019, 0027-8424
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10602 Biology , Evolutionary biology
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 9.412
RIV identification code
RIV/00216224:14110/19:00107404
Organization unit
Faculty of Medicine
UT WoS
000460242100061
Keywords in English
fibroblast growth factor; FGFR; intestinal cell kinase; ICK; cilia length
Tags
International impact, Reviewed
Změněno: 9/10/2024 14:06, Ing. Martina Blahová
Abstract
V originále
Vertebrate primary cilium is a Hedgehog signaling center but the extent of its involvement in other signaling systems is less well understood. This report delineates a mechanism by which fibroblast growth factor (FGF) controls primary cilia. Employing proteomic approaches to characterize proteins associated with the FGF-receptor, FGFR3, we identified the serine/threonine kinase intestinal cell kinase (ICK) as an FGFR interactor. ICK is involved in ciliogenesis and participates in control of ciliary length. FGF signaling partially abolished ICK's kinase activity, through FGFR-mediated ICK phosphorylation at conserved residue Tyr15, which interfered with optimal ATP binding. Activation of the FGF signaling pathway affected both primary cilia length and function in a manner consistent with cilia effects caused by inhibition of ICK activity. Moreover, knockdown and knockout of ICK rescued the FGF-mediated effect on cilia. We provide conclusive evidence that FGF signaling controls cilia via interaction with ICK.
Links
GA17-09525S, research and development project |
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GJ16-24004Y, research and development project |
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LH15231, research and development project |
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LM2015043, research and development project |
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LQ1601, research and development project |
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MUNI/A/1087/2018, interní kód MU |
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MUNI/E/0563/2018, interní kód MU |
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NV15-33232A, research and development project |
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NV15-34405A, research and development project |
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ROZV/24/LF/2018, interní kód MU |
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90043, large research infrastructures |
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