Ninein 的定位、与伙伴 dynein 和 ensconsin 的结合以及微管组织所需的结构域。

IF 3.1 3区 生物学 Q3 CELL BIOLOGY Molecular Biology of the Cell Pub Date : 2024-09-01 Epub Date: 2024-07-18 DOI:10.1091/mbc.E23-06-0245
Marisa M L Tillery, Chunfeng Zheng, Yiming Zheng, Timothy L Megraw
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引用次数: 0

摘要

Ninein(Nin)是一种微管(MT)锚,位于母中心粒的近端附属物和中心体的外周物质(PCM)上,它还能在非中心体微管组织中心(ncMTOCs)上组织微管。在人类中,NIN 基因突变会导致塞克尔综合征(一种遗传性发育障碍)。在这里,我们剖析了参与 Nin 定位以及与动力蛋白和ensconsin(ens/MAP7)相互作用的蛋白质结构域,并证明与 ens 的结合能协同调节果蝇脂肪体细胞中微管的组装。我们定义了 Nin 的结构域,这些结构域分别负责 Nin 在脂肪体细胞核表面 ncMTOC 的定位、在细胞核内的定位以及与 Dynein 轻中间链(Dlic)和 ens 的结合。我们发现,Nin 与 ens 的结合协同调控了 MT 的组装。这些发现共同揭示了 Nin 功能的新特点及其对 ncMTOC 的调控。
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Ninein domains required for its localization, association with partners dynein and ensconsin, and microtubule organization.

Ninein (Nin) is a microtubule (MT) anchor at the subdistal appendages of mother centrioles and the pericentriolar material (PCM) of centrosomes that also functions to organize MTs at noncentrosomal MT-organizing centers (ncMTOCs). In humans, the NIN gene is mutated in Seckel syndrome, an inherited developmental disorder. Here, we dissect the protein domains involved in Nin's localization and interactions with dynein and ensconsin (ens/MAP7) and show that the association with ens cooperatively regulates MT assembly in Drosophila fat body cells. We define domains of Nin responsible for its localization to the ncMTOC on the fat body cell nuclear surface, localization within the nucleus, and association with Dynein light intermediate chain (Dlic) and ens, respectively. We show that Nin's association with ens synergistically regulates MT assembly. Together, these findings reveal novel features of Nin function and its regulation of a ncMTOC.

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来源期刊
Molecular Biology of the Cell
Molecular Biology of the Cell 生物-细胞生物学
CiteScore
6.00
自引率
6.10%
发文量
402
审稿时长
2 months
期刊介绍: MBoC publishes research articles that present conceptual advances of broad interest and significance within all areas of cell, molecular, and developmental biology. We welcome manuscripts that describe advances with applications across topics including but not limited to: cell growth and division; nuclear and cytoskeletal processes; membrane trafficking and autophagy; organelle biology; quantitative cell biology; physical cell biology and mechanobiology; cell signaling; stem cell biology and development; cancer biology; cellular immunology and microbial pathogenesis; cellular neurobiology; prokaryotic cell biology; and cell biology of disease.
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