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Biology subjects

Advedissian, T.

Publications and source records attributed to Advedissian, T..

3 recordsLinked to original sources

Rotational asymmetry is required to position centrioles at the base of the primary cilium

The polarization of motile cilia requires that the centrioles, from which cilia are formed, display rotational asymmetry. This property is manifested in the presence of asymmetrically distributed appendages and relies on evolutionary conserved mechanisms. These mechanisms are also at play in cells that form primary cilia despite the lack of ciliary motility and asymmetric centriole appendages in this context. Here, we find that a complex consisting of CCDC61, KIAA1328 (K1328), and centlein (CNTLN) contributes to the establishment of centriole rotational asymmetry. In cells with a primary cilium, this complex is required for assembling a linker that repositions the daughter centriole close to and orthogonal to the proximal end of the mother centriole/basal body. The CCDC61/K1328/CNTLN complex also triggers the asymmetric recruitment of pericentriolar matrix components around newly assembled centrioles, which likely facilitates the later attachment of the basal body-daughter centriole linker. Overall, our results establish that rotational asymmetry relies on the coordinated recruitment of asymmetric landmarks along centrioles and is necessary for positioning the centrioles in a configuration that is widely conserved in ciliated cells.

cell biology↗

Cut-Detector: A Tool for Automated Temporal Analysis of Late Cytokinetic Events

Cytokinesis is the final step of cell division, resulting in the physical separation of the two daughter cells. Despite its fundamental importance in cell biology, biologists currently lack automatic tools for large-scale profiling of cytokinesis dynamics. In particular, the timing of the first microtubule cut in the intercellular bridge connecting the daughter cells is crucial, as it marks a critical step preceding abscission. Here, we introduce Cut-Detector, an open-source tool for the automatic analysis of late cytokinesis timing from time-lapse microscopy movies. Cut-Detector employs an AI approach to carry out the multiple tasks required to monitor cytokinesis: cell segmentation and tracking, detection of cell division events, localization of the intercellular bridge, and detection of the microtubule cuts. Cut-Detector will facilitate large-scale analyses to uncover new cytokinetic genes, a task that would be impractical without automation.

bioinformatics↗

Cytokinetic abscission requires actin-dependent microtubule severing

Cell division is completed by the abscission of the intercellular bridge connecting the daughter cells. Abscission requires the polymerization of an ESCRT-III cone close to the midbody to both recruit the microtubule severing enzyme spastin and scission the plasma membrane. Contrary to the common assumption, we found that the microtubule and the membrane cuts are two separate events and are regulated differently. We uncovered that the F-actin disassembling protein Cofilin-1 controls the disappearance of a transient pool of branched F-actin which is precisely assembled at the tip of the ESCRT-III cone just before the microtubule cut. Functionally, Cofilin-1 and Arp2/3-mediated branched F-actin favor abscission by promoting local severing of the microtubules but do not participate later in the membrane scission event. Mechanistically, branched F-actin functions as a physical barrier that limits ESCRT-III cone elongation and thereby favors stable spastin recruitment. Our work thus reveals that F-actin unexpectedly controls the timely and local disassembly of microtubules required for cytokinetic abscission.

cell biology↗