首页> 美国卫生研究院文献>Eukaryotic Cell >Interaction of the Aspergillus nidulans Microtubule-Organizing Center (MTOC) Component ApsB with Gamma-Tubulin and Evidence for a Role of a Subclass of Peroxisomes in the Formation of Septal MTOCs
【2h】

Interaction of the Aspergillus nidulans Microtubule-Organizing Center (MTOC) Component ApsB with Gamma-Tubulin and Evidence for a Role of a Subclass of Peroxisomes in the Formation of Septal MTOCs

机译:构巢曲霉微管组织中心(MTOC)组分ApsB与γ-微管蛋白的相互作用以及过氧化物酶体亚类在间隔MTOC形成中的作用的证据

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Peroxisomes are a diverse class of organelles involved in different physiological processes in eukaryotic cells. Although proteins imported into peroxisomes carry a peroxisomal targeting sequence at the C terminus (PTS1) or an alternative one close to the N terminus (PTS2), the protein content of peroxisomes varies drastically. Here we suggest a new class of peroxisomes involved in microtubule (MT) formation. Eukaryotic cells assemble MTs from distinct points in the cell. In the fungus Aspergillus nidulans, septum-associated microtubule-organizing centers (sMTOCs) are very active in addition to the spindle pole bodies (SPBs). Previously, we identified a novel MTOC-associated protein, ApsB (Schizosaccharomyces pombe mto1), whose absence affected MT formation from sMTOCs more than from SPBs, suggesting that the two protein complexes are organized differently. We show here that sMTOCs share at least two further components, gamma-tubulin and GcpC (S. pombe Alp6) with SPBs and found that ApsB interacts with gamma-tubulin. In addition, we discovered that ApsB interacts with the Woronin body protein HexA and is targeted to a subclass of peroxisomes via a PTS2 peroxisomal targeting sequence. The PTS2 motif was necessary for function but could be replaced with a PTS1 motif at the C terminus of ApsB. These results suggest a novel function for a subclass of peroxisomes in cytoskeletal organization.
机译:过氧化物酶体是真核细胞中参与不同生理过程的多种细胞器。尽管导入过氧化物酶体的蛋白质在C末端(PTS1)或接近N末端的另一种蛋白质(PTS2)带有过氧化物酶体靶向序列,但过氧化物酶体的蛋白质含量却大不相同。在这里,我们建议涉及微管(MT)形成的一类新的过氧化物酶体。真核细胞从细胞中的不同点组装MT。在构巢曲霉中,除纺锤极体(SPB)外,与隔膜相关的微管组织中心(sMTOC)也非常活跃。以前,我们鉴定了一种新型的与MTOC相关的蛋白ApsB(Schizosaccharomyces pombe mto1),其缺失对sMTOCs的MT形成的影响比对SPBs的影响更大,这表明这两种蛋白复合物的组织方式不同。我们在这里显示sMTOCs与SPB共享至少两个其他成分,γ-微管蛋白和GcpC(S. pombe Alp6),并发现ApsB与γ-微管蛋白相互作用。此外,我们发现ApsB与Woronin体蛋白HexA相互作用,并通过PTS2过氧化物酶体靶向序列靶向过氧化物酶体的亚类。 PTS2基序是功能所必需的,但可以在ApsB的C末端替换为PTS1基序。这些结果表明过氧化物酶体的亚类在细胞骨架组织中具有新功能。

著录项

相似文献

  • 外文文献
  • 中文文献
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号