Clathrin regulates centrosome positioning by promoting acto-myosin cortical tension in C. elegans embryos

Regulation of centrosome and spindle positioning is crucial for spatial cell division control. The one-cell Caenorhabditis elegans embryo has proven attractive for dissecting the mechanisms underlying centrosome and spindle positioning in a metazoan organism. Previous work revealed that these processes rely on an evolutionarily conserved force generator complex located at the cell cortex. This complex anchors the motor protein dynein, thus allowing cortical pulling forces to be exerted on astral microtubules emanating from microtubule organizing centers (MTOCs). Here, we report that the clathrin heavy chain CHC-1 negatively regulates pulling forces acting on centrosomes during interphase and on spindle poles during mitosis in one-cell C. elegans embryos. We establish a similar role for the cytokinesis/apoptosis/RNA-binding protein CAR-1 and uncover that CAR-1 is needed to maintain proper levels of CHC-1. We demonstrate that CHC-1 is necessary for normal organization of the cortical acto-myosin network and for full cortical tension. Furthermore, we establish that the centrosome positioning phenotype of embryos depleted of CHC-1 is alleviated by stabilizing the acto-myosin network. Conversely, we demonstrate that slight perturbations of the acto-myosin network in otherwise wild-type embryos results in excess centrosome movements resembling those in chc-1(RNAi) embryos. We developed a 2D computational model to simulate cortical rigidity-dependent pulling forces, which recapitulates the experimental data and further demonstrates that excess centrosome movements are produced at medium cortical rigidity values. Overall, our findings lead us to propose that clathrin plays a critical role in centrosome positioning by promoting acto-myosin cortical tension.

Mechanisms of centrosome separation in C. elegans

Alessandro De Simone

Centrosomes are the major microtubule organizing centers of animal cells. The two centrosomes present at the onset of mitosis must separate in a timely fashion along the nuclear envelope to ensure proper bipolar spindle assembly and thus genome stability. Microtubuleassociated motors of the kinesin-5 family are required for centrosome separation in several systems, but are partially redundant or entirely dispensable in others, where the minus-end directed motor dynein plays an important role. The mechanisms by which dynein powers centrosome separation are incompletely understood. Furthermore, the nature of the symmetry-breaking mechanisms that imbalance the forces acting on centrosomes to favor theirmovement away from each other are not known. We addressed these questions using a combination of 3D time-lapse microscopy, image processing and computational modeling to dissect centrosome separation in the polarized one-cell C. elegans embryo that entirely relies on dynein for this process. First, we have characterized the quantitative features of centrosome separation in the wild-type. Next, we compared centrosome separation between wild-type and mutant/RNAi conditions. Our analysis revealed that centrosome separation is powered by the combined action of dynein at the nuclear envelope and at the cell cortex. Moreover, we demonstrated that cortical dynein requires actomyosin contractility to separate centrosomes. These observations suggest that cortical dynein acts by harnessing anterior-directed actomyosin cortical flows initiated earlier in the cell cycle by the centrosomes themselves. To confirmthismodel, we successfully tested experimentally two of its key predictions, namely that dynein complexes flow toward the anterior together with the cortex and that the velocity of centrosome separation correlates with that of the flow of the nearby cortex. Taken together, these results demonstrate that centrosome separation is driven by nuclear and cortical dynein, where the latter acts by transmitting forces produced by the cortical actomyosin flow. To test whether this model is sufficient to explain centrosome separation, we developed a 3D computationalmodel of cytoskeleton dynamics. Indeed, predicted centrosome separation agrees quantitatively with the experimental observations in wild-type and mutant/RNAi conditions. Moreover, the qualitative predictions of the model are robust for parameter changes. Furthermore, computational simulations demonstrate that forces are intrinsically organized to move centrosomes away from each other without the need of any extrinsic symmetry-breaking mechanism. Indeed, in the case of nuclear dynein-driven separation, the position of centrosomes between the nuclear envelope and the cortex results in an asymmetric microtubule aster that leads to centrosome outward movement. In the case of cortical dynein, cortical flows are triggered by centrosomes and always move away from them, such that their forces are always directed to separate centrosomes. Therefore, this separation mechanism functions irrespective of the initial position of centrosomes along the cortex. In conclusion, in this thesis we uncover a novel organizing principle in which dynein, coupled with cell geometry and flow pattern, serves to robustly separate centrosomes and thus ensure genome stability.

EPFL2016

lis-1 is required for dynein-dependent cell division processes in C. elegans embryos

Pierre Gönczy

We investigated the role of the evolutionarily conserved protein Lis1 in cell division processes of Caenorhabditis elegans embryos. We identified apparent null alleles of lis-1, which result in defects identical to those observed after inactivation of the dynein heavy chain dhc-1, including defects in centrosome separation and spindle assembly. We raised antibodies against LIS-1 and generated transgenic animals expressing functional GFP-LIS-1. Using indirect immunofluorescence and spinning-disk confocal microscopy, we found that LIS-1 is present throughout the cytoplasm and is enriched in discrete subcellular locations, including the cell cortex, the vicinity of microtubule asters, the nuclear periphery and kinetochores. We established that lis-1 contributes to, but is not essential for, DHC-1 enrichment at specific subcellular locations. Conversely, we found that dhc-1, as well as the dynactin components dnc-1 (p150Glued) and dnc-2 (p50/dynamitin), are essential for LIS-1 targeting to the nuclear periphery, but not to the cell cortex nor to kinetochores. These results suggest that dynein and Lis1, albeit functioning in identical processes, are targeted partially independently of one another.

2004

Characterizing the localization and role of lin-5 and era-1 mRNAs in early C. elegans embryos

Zoltán Péter Spiró

Asymmetric cell division is essential for the generation of diversity during development and the function of stem cell lineages. The Caenorhabditis elegans zygote is an attractive model to investigate the mechanisms of spindle positioning during asymmetric cell division. In this polarized cell, the asymmetric distribution of cortical force generators along the antero-posterior axis and pulling on astral microtubules leads to the unequal cleavage of the one-cell embryo. The mechanisms underlying such cortical force generation are thought to act strictly at the protein level. In this thesis work we report that the mRNA encoding the cortical force generator component LIN-5 is enriched around centrosomes in early embryos, in a manner that depends on microtubules and dynein. We established that the lin-5 coding sequence is necessary and sufficient for mRNA enrichment around centrosomes in C. elegans. In addition, we found that lin-5 mRNA is mislocalized in lin-5(ev571) mutant embryos, which harbor a 9 nucleotide insertion in the coding sequence. Moreover, an intragenic revertant of lin-5(ev571), lin-5(ev571he63), also exhibits mislocalized lin-5 mRNA distribution. We demonstrated that this is accompanied by diminished pulling forces on the posterior spindle pole, suggesting that centrosomal localization of lin-5 mRNA is important for robust pulling forces. We found also that lin-5 mRNA centrosomal enrichment is slightly asymmetric during anaphase, with more transcripts present on the anterior side. We developed a novel FRAP-based assay, which revealed that lin-5 is translated/folded preferentially in the cytoplasm compared to centrosomes. Furthermore, we found that morpholino-mediated inhibition of lin-5 translation diminishes pulling forces on the posterior side during anaphase. Together, these findings lead us to propose that preferential translation/folding of lin-5 in the posterior cytoplasm following release of the mRNA from the posterior centrosome contributes to asymmetric cortical distribution of force generators, and thus to proper spindle positioning. Moreover, we found that the mRNA of an uncharacterized gene, era-1 is enriched on the anterior side of the zygote and is inherited by the anterior blastomeres. Similar to era-1 mRNA, a YFP fusion of ERA-1 protein is also asymmetrically distributed. Moreover, asymmetric distribution of both era-1 mRNA and YFP-ERA-1 protein requires the era-1 3'UTR. Furthermore, the RNA-binding protein MEX-5 is needed for both asymmetric era-1 mRNA localization and for its translational activation. Furthermore, we report that the clathrin heavy chain CHC-1 negatively regulates pulling forces acting on centrosomes during interphase and on spindle poles during mitosis in one-cell C. elegans embryos. We establish a similar role for the cytokinesis/apoptosis/RNA-binding protein CAR-1 and uncover that CAR-1 is needed to maintain normal levels of CHC-1. We demonstrate that CHC-1 is necessary for proper organization of the cortical acto-myosin network and for full cortical tension. Furthermore, we establish that the centrosome positioning phenotype of embryos depleted of CHC-1 is alleviated by stabilizing the acto-myosin network. Conversely, we demonstrate that slight perturbations of the acto-myosin network results in excess centrosome movements. Overall, our findings lead us to propose that clathrin plays a critical role in centrosome positioning by promoting acto-myosin cortical tension.