Abstract

It is known that the organization of microtubule (MT) networks in cells is orchestrated by subcellular structures named MT organizing centers (MTOCs). In this work, we use Light Sheet Fluorescence and Confocal Microscopy to investigate how the MT network surrounding the spherical yolk is arranged in the dclk2-GFP zebrafish transgenic line. We found that during epiboly the MT network is organized by multiple aster-like MTOCS. These structures form rings around the yolk sphere. Importantly, in wt embryos, aster-like MTOCs are only found upon pharmacological or genetic induction. Using our microscopy approach, we underscore the variability in the number of such asters in the transgenic line and report on the variety of global configurations of the yolk MT network. The asters’ morphology, dynamics, and their distribution in the yolk sphere are also analyzed. We propose that these features are tightly linked to epiboly timing and geometry. Key molecules are identified which support this asters role as MTOCs, where MT nucleation and growth take place. We conclude that the yolk MT network of dclk2-GFP transgenic embryos can be used as a model to organize microtubules in a spherical geometry by means of multiple MTOCs.

Highlights

  • It is known that the organization of microtubule (MT) networks in cells is orchestrated by subcellular structures named MT organizing centers (MTOCs)

  • We report evidence for the existence of a biological model of a vast MT network organized by means of multiple MT asters

  • Through the combination of Light-Sheet Fluorescence Microscopy (LSFM) and CSLM we deliver a detailed description of this MT network, which arises as a biological example for the organization of large MT networks in a spherical geometry

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Summary

Introduction

It is known that the organization of microtubule (MT) networks in cells is orchestrated by subcellular structures named MT organizing centers (MTOCs). Given its size and shape, the zebrafish yolk cell arises as an ideal model for studying how MT-based spatial organization scales with size, how it relates to geometrical constraints, and how its global architecture reshapes over time. With this aim, we have used Light-Sheet Fluorescence Microscopy (LSFM), confocal laser scanning microscopy (CLSM), and the zebrafish MT reporter line Tg(Xla.Eef1a1:dclk2a-GFP)[14] ( on noted as dclk2-GFP) to investigate the whole MT organization in the spherical yolk cell of these transgenic embryos during epiboly. We identify the presence of undescribed MT asters in the YCL in the dclk2-GFP embryos, at middle-stage epiboly We analyze their spatial dimensions, dynamics, and micron-scale architecture.

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