Abstract

Orbit, a Drosophila ortholog of microtubule plus-end enriched protein CLASP, plays an important role in many developmental processes involved in microtubule dynamics. Previous studies have shown that Orbit is required for asymmetric stem cell division and cystocyte divisions in germline cysts and for the development of microtubule networks that interconnect oocyte and nurse cells during oogenesis. Here, we examined the cellular localization of Orbit and its role in cyst formation during spermatogenesis. In male germline stem cells, distinct localization of Orbit was first observed on the spectrosome, which is a spherical precursor of the germline-specific cytoskeleton known as the fusome. In dividing stem cells and spermatogonia, Orbit was localized around centrosomes and on kinetochores and spindle microtubules. After cytokinesis, Orbit remained localized on ring canals, which are cytoplasmic bridges between the cells. Thereafter, it was found along fusomes, extending through the ring canal toward all spermatogonia in a cyst. Fusome localization of Orbit was not affected by microtubule depolymerization. Instead, our fluorescence resonance energy transfer experiments suggested that Orbit is closely associated with F-actin, which is abundantly found in fusomes. Surprisingly, F-actin depolymerization influenced neither fusome organization nor Orbit localization on the germline-specific cytoskeleton. We revealed that two conserved regions of Orbit are required for fusome localization. Using orbit hypomorphic mutants, we showed that the protein is required for ring canal formation and for fusome elongation mediated by the interaction of newly generated fusome plugs with the pre-existing fusome. The orbit mutation also disrupted ring canal clustering, which is essential for folding of the spermatogonia after cytokinesis. Orbit accumulates around centrosomes at the onset of spermatogonial mitosis and is required for the capture of one of the duplicated centrosomes onto the fusome. Moreover, Orbit is involved in the proper orientation of spindles towards fusomes during synchronous mitosis of spermatogonial cysts.

Highlights

  • IntroductionGerm cells synchronously develop as a syncytium of clonally related cells known as a cyst [1], [2]

  • In many animal species, germ cells synchronously develop as a syncytium of clonally related cells known as a cyst [1], [2]

  • After completion of the fourth round of spermatogonial divisions, the GFP-Orbit remained localized on ring canals connecting spermatocytes within a cyst (Fig. 1C)

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Summary

Introduction

Germ cells synchronously develop as a syncytium of clonally related cells known as a cyst [1], [2]. The cells within a cyst are interconnected and share a cytoplasm through intercellular bridges. Cysts originate from incomplete cytokinesis during cell division. In Drosophila oogenesis, 16 cystocytes are generated after four rounds of mitosis of a cystoblast derived from a germline stem cell (GSC); these 16 interconnected cells constitute a cyst. After cyst formation, a single cell within the 16-cell cyst will determine its fate as an oocyte. The remaining 15 cells in the cyst differentiate into nurse cells, which provide mRNA and proteins to the oocyte [1]

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