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在一分钟的时间尺度上观察前 60S 成熟过程。

Viewing pre-60S maturation at a minute's timescale.

机构信息

Institute of Molecular Biosciences, Humboldtstrasse 50/EG, University of Graz, A-8010 Graz, Austria.

Lehrstuhl Biochemie III, University Regensburg, Universitätsstrasse 31, 93053 Regensburg, Germany.

出版信息

Nucleic Acids Res. 2018 Apr 6;46(6):3140-3151. doi: 10.1093/nar/gkx1293.

Abstract

The formation of ribosomal subunits is a highly dynamic process that is initiated in the nucleus and involves more than 200 trans-acting factors, some of which accompany the pre-ribosomes into the cytoplasm and have to be recycled into the nucleus. The inhibitor diazaborine prevents cytoplasmic release and recycling of shuttling pre-60S maturation factors by inhibiting the AAA-ATPase Drg1. The failure to recycle these proteins results in their depletion in the nucleolus and halts the pathway at an early maturation step. Here, we made use of the fast onset of inhibition by diazaborine to chase the maturation path in real-time from 27SA2 pre-rRNA containing pre-ribosomes localized in the nucleolus up to nearly mature 60S subunits shortly after their export into the cytoplasm. This allows for the first time to put protein assembly and disassembly reactions as well as pre-rRNA processing into a chronological context unraveling temporal and functional linkages during ribosome maturation.

摘要

核糖体亚基的形成是一个高度动态的过程,起始于细胞核,涉及 200 多种反式作用因子,其中一些伴随前核糖体进入细胞质,并必须被重新循环到细胞核中。抑制剂二氮杂硼抑制 AAA-ATP 酶 Drg1,阻止穿梭前 60S 成熟因子的细胞质释放和再循环。这些蛋白质的循环失败导致它们在核仁中耗尽,并在早期成熟步骤中停止该途径。在这里,我们利用二氮杂硼的快速抑制作用,从含有定位于核仁的 27SA2 前 rRNA 的前核糖体的成熟途径进行实时追踪,直到它们几乎成熟的 60S 亚基在细胞质中输出后不久。这使得首次能够将蛋白质组装和拆卸反应以及前 rRNA 加工置于时间顺序背景中,揭示核糖体成熟过程中的时间和功能联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f600/5888160/6c8f6384b226/gkx1293fig1.jpg

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