Published February 2025 | Version Published
Journal Article Open

Interactions of N- and C-terminal parts of Ana1 permitting centriole duplication but not elongation

  • 1. ROR icon California Institute of Technology
  • 2. ROR icon Babeș-Bolyai University
  • 3. ROR icon University of Cambridge

Abstract

The conserved process of centriole duplication requires the establishment of a Sas6-centred cartwheel initiated by Plk4's phosphorylation of Ana1/STIL. Subsequently, the centriole undergoes conversion to a centrosome requiring its radial expansion and elongation, mediated by a network requiring interactions between Cep135, Ana1/Cep295 and Asterless/Cep152. Here, we show that mutant alleles encoding overlapping N- and C-terminal parts of Ana1 are capable of intragenic complementation to rescue radial expansion. This permits the recruitment of Asl and thereby centriole duplication and mechanosensory cilia formation to restore the coordination defects of these mutants. This genetic combination also rescues centriole duplication in the male germ line but does not rescue the elongation of the triplet microtubule-containing centrioles of primary spermatocytes. Consequently, these males are coordinated but sterile. Such centriole elongation is rescued by the continuous, full-length Ana1 sequence. We define a region that when deleted within otherwise intact Ana1 does not permit primary spermatocyte centrioles to elongate but still allows recruitment of Asl. Our findings point to differing demands upon the physical organization of Ana1 for the distinct processes of radial expansion and elongation of centrioles.

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Acknowledgement

We are grateful to Pallavi Panda, Paula Coelho and Ines Baiao-Santos for their comments on the manuscript and, together with all members of the Glover lab, for stimulating discussions. We are grateful to Dr Andres Collazo and Dr Giada Spigolon of the Biological Imaging Facility at Caltech for their support and to Caltech Beckman Institute Cryo-EM Facility for the use of the Tecnai electron microscope.

Funding

DMG is grateful for past support in Cambridge from the Wellcome Trust and currently in Pasadena from the National Institute of Neurological Disorders and Stroke of the National Institutes of Health under award R01NS113930.

Supplemental Material

Electronic supplementary material is available online at https://doi.org/10.6084/m9.figshare.c.7632409

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Additional details

Identifiers

Related works

Has version
Journal Article: PMC11793955 (PMCID)
Is new version of
Discussion Paper: 10.1101/2024.10.28.620588 (DOI)
Is supplemented by
Dataset: 10.6084/m9.figshare.c.7632409 (DOI)

Funding

Wellcome Trust
National Institutes of Health
R01NS113930

Dates

Accepted
2025-01-09
Available
2025-02-05
Published

Caltech Custom Metadata

Caltech groups
Division of Biology and Biological Engineering (BBE)
Publication Status
Published