Regulation of Xvelo assembly by centrosomal proteins

The oocyte Balbiani body (Bb) is a conserved membraneless organelle required for germline specification in many species. Here we report that when overexpressed in mammalian somatic cells, <i>Xenopus</i> Velo (Xvelo), the Bb matrix protein could reconstitute a "Bb-like" structure, which shares key features of the oocyte Bb. Using this system, we investigated the potential mechanism of Bb assembly. We focused on the involvement of centrosomal proteins in this process, as both endogenous oocyte Bb and the "Bb-like" structure induced by Xvelo overexpression form around the centrosome. Our results reveal that multiple components of the centrosome can interact with Xvelo and promote Xvelo assembly to varying degrees. Moreover, knockdown of these proteins reduces Xvelo assembly. Our findings thus suggest that the interaction between centrosomal proteins and Xvelo may facilitate the initial aggregation of Xvelo, leading to the assembly of Bb around the centrosome in the oocyte.

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Journal
iScience
Published
2025-10-17
DOI
https://doi.org/10.1016/j.isci.2025.113805
Primary Topic
Microtubule and mitosis dynamics
Type
article
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article

Regulation of Xvelo assembly by centrosomal proteins

Elvan Böke, Meining Li, Divyanshi Divyanshi, Jing Yang
iScience
Microtubule and mitosis dynamics
article

Regulation of Xvelo assembly by centrosomal proteins

Elvan Böke, Meining Li, Divyanshi Divyanshi, Jing Yang
article en

Abstract

The oocyte Balbiani body (Bb) is a conserved membraneless organelle required for germline specification in many species. Here we report that when overexpressed in mammalian somatic cells, <i>Xenopus</i> Velo (Xvelo), the Bb matrix protein could reconstitute a "Bb-like" structure, which shares key features of the oocyte Bb. Using this system, we investigated the potential mechanism of Bb assembly. We focused on the involvement of centrosomal proteins in this process, as both endogenous oocyte Bb and the "Bb-like" structure induced by Xvelo overexpression form around the centrosome. Our results reveal that multiple components of the centrosome can interact with Xvelo and promote Xvelo assembly to varying degrees. Moreover, knockdown of these proteins reduces Xvelo assembly. Our findings thus suggest that the interaction between centrosomal proteins and Xvelo may facilitate the initial aggregation of Xvelo, leading to the assembly of Bb around the centrosome in the oocyte.

iScienceVol. 28(11)
Institució Catalana de Recerca i Estudis Avançats (ES), University of Illinois Urbana-Champaign (US), Centre for Genomic Regulation (ES)
Openalex Percentile: Top 69%
Microtubule and mitosis dynamics
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