Cilium structure, assembly, and disassembly regulated by the cytoskeleton
The cilium, once considered a vestigial structure, is a conserved, microtubule-based
organelle critical for transducing extracellular chemical and mechanical signals that control …
organelle critical for transducing extracellular chemical and mechanical signals that control …
Mechanism of ciliary disassembly
Y Liang, D Meng, B Zhu, J Pan - Cellular and Molecular Life Sciences, 2016 - Springer
As motile organelles and sensors, cilia play pivotal roles in cell physiology, development
and organ homeostasis. Ciliary defects are associated with a class of cilia-related diseases …
and organ homeostasis. Ciliary defects are associated with a class of cilia-related diseases …
CEP104/FAP256 and associated cap complex maintain stability of the ciliary tip
T Legal, M Parra, M Tong, CS Black… - Journal of Cell …, 2023 - rupress.org
Cilia are essential organelles that protrude from the cell body. Cilia are made of a
microtubule-based structure called the axoneme. In most types of cilia, the ciliary tip is …
microtubule-based structure called the axoneme. In most types of cilia, the ciliary tip is …
A human ciliopathy reveals essential functions for NEK10 in airway mucociliary clearance
Mucociliary clearance, the physiological process by which mammalian conducting airways
expel pathogens and unwanted surface materials from the respiratory tract, depends on the …
expel pathogens and unwanted surface materials from the respiratory tract, depends on the …
The multifaceted roles of microtubule-associated proteins in the primary cilium and ciliopathies
J Deretic, E Odabasi… - Journal of Cell …, 2023 - journals.biologists.com
The primary cilium is a conserved microtubule-based organelle that is critical for transducing
developmental, sensory and homeostatic signaling pathways. It comprises an axoneme with …
developmental, sensory and homeostatic signaling pathways. It comprises an axoneme with …
Transition zone assembly and its contribution to axoneme formation in Drosophila male germ cells
J Vieillard, M Paschaki, JL Duteyrat, C Augière… - Journal of Cell …, 2016 - rupress.org
The ciliary transition zone (TZ) is a complex structure found at the cilia base. Defects in TZ
assembly are associated with human ciliopathies. In most eukaryotes, three protein …
assembly are associated with human ciliopathies. In most eukaryotes, three protein …
Single-particle imaging reveals intraflagellar transport–independent transport and accumulation of EB1 in Chlamydomonas flagella
JA Harris, Y Liu, P Yang, P Kner… - Molecular biology of the …, 2016 - Am Soc Cell Biol
The microtubule (MT) plus-end tracking protein EB1 is present at the tips of cilia and flagella;
end-binding protein 1 (EB1) remains at the tip during flagellar shortening and in the absence …
end-binding protein 1 (EB1) remains at the tip during flagellar shortening and in the absence …
Cytoskeletal networks in primary cilia: Current knowledge and perspectives
R Ge, M Cao, M Chen, M Liu… - Journal of Cellular …, 2022 - Wiley Online Library
Primary cilia, microtubule‐based protrusions present on the surface of most mammalian
cells, function as sensory organelles that monitor extracellular signals and transduce them …
cells, function as sensory organelles that monitor extracellular signals and transduce them …
Length-dependent disassembly maintains four different flagellar lengths in Giardia
With eight flagella of four different lengths, the parasitic protist Giardia is an ideal model to
evaluate flagellar assembly and length regulation. To determine how four different flagellar …
evaluate flagellar assembly and length regulation. To determine how four different flagellar …
Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly Syndrome
Short-rib polydactyly syndromes (SRPS) and Asphyxiating thoracic dystrophy (ATD) or
Jeune Syndrome are recessively inherited skeletal ciliopathies characterized by profound …
Jeune Syndrome are recessively inherited skeletal ciliopathies characterized by profound …