Publications by authors named "M Le Guennec"

Article Synopsis
  • Cilia assembly in metazoans involves crucial steps such as centriole maturation, migration to the cell surface, and docking with the plasma membrane; mutations affecting these processes are linked to severe ciliopathies.* -
  • The study uses Paramecium as a model organism to discover that proteins CEP90, FOPNL, and OFD1 are essential for ciliogenesis and are conserved across different species.* -
  • The research reveals that these proteins localize at the distal ends of centrioles/basal bodies and require an additional component, Moonraker (MNR), for proper recruitment and assembly in mammalian cells.*
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Centrioles are evolutionarily conserved barrels of microtubule triplets that form the core of the centrosome and the base of the cilium. While the crucial role of the proximal region in centriole biogenesis has been well documented, its native architecture and evolutionary conservation remain relatively unexplored. Here, using cryo-electron tomography of centrioles from four evolutionarily distant species, we report on the architectural diversity of the centriole's proximal cartwheel-bearing region.

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Centrioles are polarized microtubule-based organelles that seed the formation of cilia, and which assemble from a cartwheel containing stacked ring oligomers of SAS-6 proteins. A cryo-tomography map of centrioles from the termite flagellate Trichonympha spp. was obtained previously, but higher resolution analysis is likely to reveal novel features.

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Centrioles are characterized by a nine-fold arrangement of microtubule triplets held together by an inner protein scaffold. These structurally robust organelles experience strenuous cellular processes such as cell division or ciliary beating while performing their function. However, the molecular mechanisms underlying the stability of microtubule triplets, as well as centriole architectural integrity remain poorly understood.

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Super-resolution microscopies have become an established tool in biological research. However, imaging throughput remains a main bottleneck in acquiring large datasets required for quantitative biology. Here we describe multifocal flat illumination for field-independent imaging (mfFIFI).

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