Unknown

Dataset Information

0

Cell-free reconstitution reveals centriole cartwheel assembly mechanisms.


ABSTRACT: How cellular organelles assemble is a fundamental question in biology. The centriole organelle organizes around a nine-fold symmetrical cartwheel structure typically ?100?nm high comprising a stack of rings that each accommodates nine homodimers of SAS-6 proteins. Whether nine-fold symmetrical ring-like assemblies of SAS-6 proteins harbour more peripheral cartwheel elements is unclear. Furthermore, the mechanisms governing ring stacking are not known. Here we develop a cell-free reconstitution system for core cartwheel assembly. Using cryo-electron tomography, we uncover that the Chlamydomonas reinhardtii proteins CrSAS-6 and Bld10p together drive assembly of the core cartwheel. Moreover, we discover that CrSAS-6 possesses autonomous properties that ensure self-organized ring stacking. Mathematical fitting of reconstituted cartwheel height distribution suggests a mechanism whereby preferential addition of pairs of SAS-6 rings governs cartwheel growth. In conclusion, we have developed a cell-free reconstitution system that reveals fundamental assembly principles at the root of centriole biogenesis.

SUBMITTER: Guichard P 

PROVIDER: S-EPMC5376648 | biostudies-literature | 2017 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

Cell-free reconstitution reveals centriole cartwheel assembly mechanisms.

Guichard P P   Hamel V V   Le Guennec M M   Banterle N N   Iacovache I I   Nemčíková V V   Flückiger I I   Goldie K N KN   Stahlberg H H   Lévy D D   Zuber B B   Gönczy P P  

Nature communications 20170323


How cellular organelles assemble is a fundamental question in biology. The centriole organelle organizes around a nine-fold symmetrical cartwheel structure typically ∼100 nm high comprising a stack of rings that each accommodates nine homodimers of SAS-6 proteins. Whether nine-fold symmetrical ring-like assemblies of SAS-6 proteins harbour more peripheral cartwheel elements is unclear. Furthermore, the mechanisms governing ring stacking are not known. Here we develop a cell-free reconstitution s  ...[more]

Similar Datasets

| S-EPMC4116473 | biostudies-literature
| S-EPMC3655416 | biostudies-literature
| S-EPMC8346886 | biostudies-literature
| S-SCDT-10_1038-S44319-024-00157-Y | biostudies-other
| S-EPMC7667884 | biostudies-literature
| S-EPMC7667878 | biostudies-literature
| S-EPMC3871432 | biostudies-literature
| S-EPMC4152953 | biostudies-literature
| S-EPMC8136855 | biostudies-literature
| S-EPMC3941056 | biostudies-literature