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体外核重建:围绕无蛋白质DNA的组装阶段。

Nuclear reconstitution in vitro: stages of assembly around protein-free DNA.

作者信息

Newport J

出版信息

Cell. 1987 Jan 30;48(2):205-17. doi: 10.1016/0092-8674(87)90424-7.

Abstract

We have developed a cell-free system derived from Xenopus eggs that reconstitutes nuclear structure around an added protein-free substrate (bacteriophage lambda DNA). Assembled nuclei are morphologically indistinguishable from normal eukaryotic nuclei: they are surrounded by a double membrane containing nuclear pores and are lined with a peripheral nuclear lamina. Nuclear assembly involves discrete intermediate steps, including nucleosome assembly, scaffold assembly, and nuclear membrane and lamina assembly, indicating that during reconstitution nuclear organization is assembled one level at a time. Topoisomerase II inhibitors block nuclear assembly. Lamin proteins and membrane vesicles bind to chromatin late in assembly, suggesting that these components do not interact with chromatin that is formed early in assembly. Reconstituted nuclei replicate their DNA; replication begins only after envelope formation has initiated, indicating that envelope attachment may be important for regulating replication.

摘要

我们开发了一种源自非洲爪蟾卵的无细胞系统,该系统能在添加的无蛋白质底物(噬菌体λDNA)周围重建核结构。组装好的细胞核在形态上与正常真核细胞核无法区分:它们被含有核孔的双层膜包围,并内衬有核周层。核组装涉及离散的中间步骤,包括核小体组装、支架组装以及核膜和层组装,这表明在重建过程中,核组织是一级一级组装起来的。拓扑异构酶II抑制剂会阻断核组装。核纤层蛋白和膜泡在组装后期与染色质结合,这表明这些成分不会与组装早期形成的染色质相互作用。重建的细胞核能复制其DNA;复制仅在包膜形成开始后才启动,这表明包膜附着可能对调节复制很重要。

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