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Proteolytic control in ciliogenesis: Temporal restriction or early initiation?

Cellular processes are highly dependent on a dynamic proteome that undergoes structural and functional rearrangements to allow swift conversion between different cellular states. By inducing proteasomal degradation of inhibitory or stimulating factors, ubiquitylation is particularly well suited to t...

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Bibliographic Details
Published in:BioEssays 2022-09, Vol.44 (9), p.e2200087-n/a
Main Authors: Habeck, Gregor, Schweiggert, Jörg
Format: Article
Language:English
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Summary:Cellular processes are highly dependent on a dynamic proteome that undergoes structural and functional rearrangements to allow swift conversion between different cellular states. By inducing proteasomal degradation of inhibitory or stimulating factors, ubiquitylation is particularly well suited to trigger such transitions. One prominent example is the remodelling of the centrosome upon cell cycle exit, which is required for the formation of primary cilia – antenna‐like structures on the surface of most cells that act as integrative hubs for various extracellular signals. Over the last decade, many reports on ubiquitin‐related events involved in the regulation of ciliogenesis have emerged. Very often, these processes are considered to be initiated ad hoc, that is, directly before its effect on cilia biogenesis becomes evident. While such a temporal restriction may hold true for the majority of events, there is evidence that some of them are initiated earlier during the cell cycle. Here, we provide an overview of ubiquitin‐dependent processes in ciliogenesis and discuss available data that indicate such an early onset of proteolytic regulation within preceding cell cycle stages. Ubiquitin‐dependent regulation of ciliogenesis via proteasomal degradation is considered to be temporally restricted to the beginning of cellular quiescence. In this review, we discuss published data suggesting that some proteolytic processes are initiated earlier within cell cycle stages preceding G0.
ISSN:0265-9247
1521-1878
DOI:10.1002/bies.202200087