scholarly journals The ciliopathy gene product Cep290 is required for primary cilium formation and microtubule network organization

2018 ◽  
Vol 42 (5) ◽  
pp. 371-381
Author(s):  
Elif Nur FIRAT-KARALAR
Author(s):  
Leticia Labat-de-Hoz ◽  
Armando Rubio-Ramos ◽  
Javier Casares-Arias ◽  
Miguel Bernabé-Rubio ◽  
Isabel Correas ◽  
...  

Primary cilia are solitary, microtubule-based protrusions surrounded by a ciliary membrane equipped with selected receptors that orchestrate important signaling pathways that control cell growth, differentiation, development and homeostasis. Depending on the cell type, primary cilium assembly takes place intracellularly or at the cell surface. The intracellular route has been the focus of research on primary cilium biogenesis, whereas the route that occurs at the cell surface, which we call the “alternative” route, has been much less thoroughly characterized. In this review, based on recent experimental evidence, we present a model of primary ciliogenesis by the alternative route in which the remnant of the midbody generated upon cytokinesis acquires compact membranes, that are involved in compartmentalization of biological membranes. The midbody remnant delivers part of those membranes to the centrosome in order to assemble the ciliary membrane, thereby licensing primary cilium formation. The midbody remnant's involvement in primary cilium formation, the regulation of its inheritance by the ESCRT machinery, and the assembly of the ciliary membrane from the membranes originally associated with the remnant are discussed in the context of the literature concerning the ciliary membrane, the emerging roles of the midbody remnant, the regulation of cytokinesis, and the role of membrane compartmentalization. We also present a model of cilium emergence during evolution, and summarize the directions for future research.


Development ◽  
2000 ◽  
Vol 127 (19) ◽  
pp. 4253-4264 ◽  
Author(s):  
N.C. Grieder ◽  
M. de Cuevas ◽  
A.C. Spradling

Differentiation of the Drosophila oocyte takes place in a cyst of 16 interconnected germ cells and is dependent on a network of microtubules that becomes polarized as differentiation progresses (polarization). We have investigated how the microtubule network polarizes using a GFP-tubulin construct that allows germ-cell microtubules to be visualized with greater sensitivity than in previous studies. Unexpectedly, microtubules are seen to associate with the fusome, an asymmetric germline-specific organelle, which elaborates as cysts form and undergoes complex changes during cyst polarization. This fusome-microtubule association occurs periodically during late interphases of cyst divisions and then continuously in 16-cell cysts that have entered meiotic prophase. As meiotic cysts move through the germarium, microtubule minus ends progressively focus towards the center of the fusome, as visualized using a NOD-lacZ marker. During this same period, discrete foci rich in gamma tubulin that very probably correspond to migrating cystocyte centrosomes also associate with the fusome, first on the fusome arms and then in its center, subsequently moving into the differentiating oocyte. The fusome is required for this complex process, because microtubule network organization and polarization are disrupted in hts(1) mutant cysts, which lack fusomes. Our results suggest that the fusome, a specialized membrane-skeletal structure, which arises in early germ cells, plays a crucial role in polarizing 16-cell cysts, at least in part by interacting with microtubules and centrosomes.


2020 ◽  
Vol 107 (6) ◽  
pp. 625-635
Author(s):  
Dong Ding ◽  
Xiao Yang ◽  
Hui-qin Luan ◽  
Xin-tong Wu ◽  
Cai He ◽  
...  

2004 ◽  
Vol 66 (4) ◽  
pp. 1345-1355 ◽  
Author(s):  
Luís F.C. Menezes ◽  
Yiqiang Cai ◽  
Yasuyuki Nagasawa ◽  
Ana M.G. Silva ◽  
Mary L. Watkins ◽  
...  

2006 ◽  
Vol 16 (2) ◽  
pp. 173-186 ◽  
Author(s):  
Helen R. Dawe ◽  
Ursula M. Smith ◽  
Andrew R. Cullinane ◽  
Dianne Gerrelli ◽  
Phillip Cox ◽  
...  

2017 ◽  
Vol 131 (1) ◽  
pp. jcs208769 ◽  
Author(s):  
Kengo Takahashi ◽  
Tomoaki Nagai ◽  
Shuhei Chiba ◽  
Keiko Nakayama ◽  
Kensaku Mizuno

2020 ◽  
Vol 390 (2) ◽  
pp. 111952 ◽  
Author(s):  
Yunkai Qie ◽  
Lin Wang ◽  
E. Du ◽  
Shuaiqi Chen ◽  
Chao Lu ◽  
...  

2011 ◽  
Vol 22 (6) ◽  
pp. 806-816 ◽  
Author(s):  
Neeraj Sharma ◽  
Zachary A. Kosan ◽  
Jannese E. Stallworth ◽  
Nicolas F. Berbari ◽  
Bradley K. Yoder

The primary cilium is an evolutionarily conserved dynamic organelle important for regulating numerous signaling pathways, and, as such, mutations disrupting ciliogenesis result in a variety of developmental abnormalities and postnatal disorders. The length of the cilium is regulated by the cell through largely unknown mechanisms. Normal cilia length is important, as either shortened or elongated cilia have been associated with disease and developmental defects. Here we explore the importance of cytoskeletal dynamics in regulating cilia length. Using pharmacological approaches in different cell types, we demonstrate that actin depolymerization or stabilization and protein kinase A activation result in a rapid elongation of the primary cilium. The effects of pharmacological agents on cilia length are associated with a subsequent increase in soluble tubulin levels and can be impaired by depletion of soluble tubulin with taxol. In addition, subtle nocodazole treatment was able to induce ciliogenesis under conditions in which cilia are not normally formed and also increases cilia length on cells that have already established cilia. Together these data indicate that cilia length can be regulated through changes in either the actin or microtubule network and implicate a possible role for soluble tubulin levels in cilia length control.


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