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精子发生过程中的核伸长依赖于果蝇 Mst27D 将核孔复合物与束状微管物理连接。

Nuclear elongation during spermiogenesis depends on physical linkage of nuclear pore complexes to bundled microtubules by Drosophila Mst27D.

机构信息

Department of Molecular Life Science (DMLS), University of Zurich, Zurich, Switzerland.

出版信息

PLoS Genet. 2023 Jul 10;19(7):e1010837. doi: 10.1371/journal.pgen.1010837. eCollection 2023 Jul.

Abstract

Spermatozoa in animal species are usually highly elongated cells with a long motile tail attached to a head that contains the haploid genome in a compact and often elongated nucleus. In Drosophila melanogaster, the nucleus is compacted two hundred-fold in volume during spermiogenesis and re-modeled into a needle that is thirty-fold longer than its diameter. Nuclear elongation is preceded by a striking relocalization of nuclear pore complexes (NPCs). While NPCs are initially located throughout the nuclear envelope (NE) around the spherical nucleus of early round spermatids, they are later confined to one hemisphere. In the cytoplasm adjacent to this NPC-containing NE, the so-called dense complex with a strong bundle of microtubules is assembled. While this conspicuous proximity argued for functional significance of NPC-NE and microtubule bundle, experimental confirmation of their contributions to nuclear elongation has not yet been reported. Our functional characterization of the spermatid specific Mst27D protein now resolves this deficit. We demonstrate that Mst27D establishes physical linkage between NPC-NE and dense complex. The C-terminal region of Mst27D binds to the nuclear pore protein Nup358. The N-terminal CH domain of Mst27D, which is similar to that of EB1 family proteins, binds to microtubules. At high expression levels, Mst27D promotes bundling of microtubules in cultured cells. Microscopic analyses indicated co-localization of Mst27D with Nup358 and with the microtubule bundles of the dense complex. Time-lapse imaging revealed that nuclear elongation is accompanied by a progressive bundling of microtubules into a single elongated bundle. In Mst27D null mutants, this bundling process does not occur and nuclear elongation is abnormal. Thus, we propose that Mst27D permits normal nuclear elongation by promoting the attachment of the NPC-NE to the microtubules of the dense complex, as well as the progressive bundling of these microtubules.

摘要

在动物物种中,精子通常是高度细长的细胞,带有一个长的能动尾巴,连接到一个头部,头部中的单倍体基因组在一个紧凑且通常细长的核中。在黑腹果蝇中,在精子发生过程中,核体积压缩了 200 倍,并重塑成一个比其直径长 30 倍的针状结构。核伸长之前,核孔复合物 (NPC) 发生明显的重新定位。虽然 NPC 最初位于早期圆形精子细胞的球形核周围的核包膜 (NE) 中,但后来它们被限制在一个半球内。在含有 NPC 的 NE 相邻的细胞质中,组装了所谓的具有强烈微管束的致密复合物。虽然这种明显的接近表明 NPC-NE 和微管束的功能重要性,但尚未报道实验证实它们对核伸长的贡献。我们对精子特异性 Mst27D 蛋白的功能表征现在解决了这一不足。我们证明 Mst27D 在 NPC-NE 和致密复合物之间建立了物理连接。Mst27D 的 C 端区域与核孔蛋白 Nup358 结合。Mst27D 的 N 端 CH 结构域与 EB1 家族蛋白相似,与微管结合。在高表达水平下,Mst27D 促进培养细胞中微管的束状排列。显微镜分析表明 Mst27D 与 Nup358 和致密复合物的微管束共定位。延时成像显示核伸长伴随着微管逐渐束状排列成单个细长束。在 Mst27D 缺失突变体中,该束状过程不会发生,核伸长异常。因此,我们提出 Mst27D 通过促进 NPC-NE 与致密复合物的微管的附着以及这些微管的渐进束状排列,允许正常的核伸长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11d6/10359004/a31e52fd888d/pgen.1010837.g001.jpg

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