Detailed Information on Publication Record
2020
KIF14 controls ciliogenesis via regulation of Aurora A and is important for Hedgehog signaling
PEJŠKOVÁ, Petra, Madeline Louise REILLY, Lucia BINÓ, Ondřej BERNATÍK, Linda DOLANSKÁ et. al.Basic information
Original name
KIF14 controls ciliogenesis via regulation of Aurora A and is important for Hedgehog signaling
Authors
PEJŠKOVÁ, Petra (203 Czech Republic, belonging to the institution), Madeline Louise REILLY (250 France), Lucia BINÓ (703 Slovakia, belonging to the institution), Ondřej BERNATÍK (203 Czech Republic, belonging to the institution), Linda DOLANSKÁ (203 Czech Republic, belonging to the institution), Sri Ranjani GANJI (356 India), Zbyněk ZDRÁHAL (203 Czech Republic), Alexandre BENMERAH (250 France) and Lukáš ČAJÁNEK (203 Czech Republic, guarantor, belonging to the institution)
Edition
JOURNAL OF CELL BIOLOGY, New York, ROCKEFELLER UNIVERSITY PRESS, 2020, 0021-9525
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10601 Cell biology
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 10.539
RIV identification code
RIV/00216224:14110/20:00114130
Organization unit
Faculty of Medicine
UT WoS
000538141100021
Keywords in English
PRIMARY CILIUM; MOTHER CENTRIOLE; MOTOR PROTEINS; SONIC HEDGEHOG; EARLY STEPS; KINESIN-II; CELL-CYCLE; A KINASE; ACTIVATION; CEP164
Tags
International impact, Reviewed
Změněno: 10/10/2024 13:52, Ing. Martina Blahová
Abstract
V originále
Primary cilia play critical roles in development and disease. Their assembly and disassembly are tightly coupled to cell cycle progression. Here, we present data identifying KIF14 as a regulator of cilia formation and Hedgehog (HH) signaling. We show that RNAi depletion of KIF14 specifically leads to defects in ciliogenesis and basal body (BB) biogenesis, as its absence hampers the efficiency of primary cilium formation and the dynamics of primary cilium elongation, and disrupts the localization of the distal appendage proteins SCLT1 and FBF1 and components of the IFT-B complex. We identify deregulated Aurora A activity as a mechanism contributing to the primary cilium and BB formation defects seen after KIF14 depletion. In addition, we show that primary cilia in KIF14-depleted cells are defective in response to HH pathway activation, independently of the effects of Aurora A. In sum, our data point to KIF14 as a critical node connecting cell cycle machinery, effective ciliogenesis, and HH signaling.
Links
GA19-05244S, research and development project |
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GJ16-03269Y, research and development project |
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LM2018127, research and development project |
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LQ1601, research and development project |
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90127, large research infrastructures |
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90129, large research infrastructures |
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