Conserved structural motifs in the central pair complex of eukaryotic flagella

説明

<jats:title>Abstract</jats:title><jats:p>Cilia and flagella are conserved hair‐like appendages of eukaryotic cells that function as sensing and motility generating organelles. Motility is driven by thousands of axonemal dyneins that require precise regulation. One essential motility regulator is the central pair complex (CPC) and many CPC defects cause paralysis of cilia/flagella. Several human diseases, such as immotile cilia syndrome, show CPC abnormalities, but little is known about the detailed three‐dimensional (3D) structure and function of the CPC. The CPC is located in the center of typical [9+2] cilia/flagella and is composed of two singlet microtubules (MTs), each with a set of associated projections that extend toward the surrounding nine doublet MTs. Using cryo‐electron tomography coupled with subtomogram averaging, we visualized and compared the 3D structures of the CPC in both the green alga <jats:italic>Chlamydomonas</jats:italic> and the sea urchin <jats:italic>Strongylocentrotus</jats:italic> at the highest resolution published to date. Despite the evolutionary distance between these species, their CPCs exhibit remarkable structural conservation. We identified several new projections, including those that form the elusive sheath, and show that the bridge has a more complex architecture than previously thought. Organism‐specific differences include the presence of MT inner proteins in <jats:italic>Chlamydomonas</jats:italic>, but not <jats:italic>Strongylocentrotus</jats:italic>, and different overall outlines of the highly connected projection network, which forms a round‐shaped cylinder in algae, but is more oval in sea urchin. These differences could be adaptations to the mechanical requirements of the rotating CPC in <jats:italic>Chlamydomonas</jats:italic>, compared to the <jats:italic>Strongylocentrotus</jats:italic> CPC which has a fixed orientation. © 2012 Wiley Periodicals, Inc</jats:p>

収録刊行物

  • Cytoskeleton

    Cytoskeleton 70 (2), 101-120, 2012-12-26

    Wiley

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