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Orbit/CLASP Is Required for Germline Cyst Formation through Its Developmental Control of Fusomes and Ring Canals in Drosophila Males

机译:在果蝇男性Fusomes和环运河的轨道/表扣所需的种系囊肿形成通过其发育调控

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摘要

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.
机译:Orbit是果蝇直向同源的微管末端富集蛋白CLASP,在涉及微管动力学的许多发育过程中起着重要作用。先前的研究表明,在种系囊肿中不对称的干细胞分裂和囊状细胞分裂,以及在卵子发生过程中连接卵母细胞和护士细胞的微管网络的发展,都需要Orbit。在这里,我们检查了在生精过程中眼眶的细胞定位及其在囊肿形成中的作用。在雄性种系干细胞中,首先在光谱体上观察到了轨道的独特定位,该光谱体是种系特异性细胞骨架的球形前体,称为球状体。在分裂干细胞和精原细胞时,眼眶位于中心体周围,动植物和纺锤体微管上。胞质分裂后,Orbit仍位于环管中,环管是细胞之间的细胞质桥。此后,沿着纤维体发现了它,穿过囊管向囊肿中的所有精原细胞延伸。微管解聚不会影响眼眶的局部定位。相反,我们的荧光共振能量转移实验表明Orbit与F-肌动蛋白密切相关,F-肌动蛋白在烟熏质中含量很高。出人意料的是,F-肌动蛋白解聚既不会影响种系特异性细胞骨架上的脂质体组织也不会影响其轨道定位。我们揭示了模糊定位需要两个保守的轨道区域。我们使用轨道亚型突变体,表明该蛋白是环管形成和新产生的fusome塞子与先前存在的fusome相互作用介导的fusome延伸所必需的。轨道突变还会破坏环管聚集,这对于胞质分裂后精原细胞的折叠必不可少。在精原体的有丝分裂开始时,轨道就在中心体附近积累,这是将复制的中心体之一捕获到体形体中所必需的。此外,在精原性囊肿的同步有丝分裂过程中,轨道参与纺锤体向纺锤体的正确定向。

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