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天生用于输出:不同强度的羧基末端核输出信号确保核磷蛋白白血病突变体在细胞质中积累。

Born to be exported: COOH-terminal nuclear export signals of different strength ensure cytoplasmic accumulation of nucleophosmin leukemic mutants.

作者信息

Bolli Niccolò, Nicoletti Ildo, De Marco M Felicetta, Bigerna Barbara, Pucciarini Alessandra, Mannucci Roberta, Martelli Maria Paola, Liso Arcangelo, Mecucci Cristina, Fabbiano Francesco, Martelli Massimo F, Henderson Beric R, Falini Brunangelo

机构信息

Section of Hematology and Immunology, University of Perugia, Perugia, Italy.

出版信息

Cancer Res. 2007 Jul 1;67(13):6230-7. doi: 10.1158/0008-5472.CAN-07-0273.

Abstract

Creation of a nuclear export signal (NES) motif and loss of tryptophans (W) 288 and 290 (or 290 only) at the COOH terminus of nucleophosmin (NPM) are both crucial for NPM aberrant cytoplasmic accumulation in acute myelogenous leukemia (AML) carrying NPM1 mutations. Hereby, we clarify how these COOH-terminal alterations functionally cooperate to delocalize NPM to the cytoplasm. Using a Rev(1.4)-based shuttling assay, we measured the nuclear export efficiency of six different COOH-terminal NES motifs identified in NPM mutants and found significant strength variability, the strongest NES motifs being associated with NPM mutants retaining W288. When artificially coupled with a weak NES, W288-retaining NPM mutants are not exported efficiently into cytoplasm because the force (W288) driving the mutants toward the nucleolus overwhelms the force (NES) exporting the mutants into cytoplasm. We then used this functional assay to study the physiologic NH(2)-terminal NES motifs of wild-type NPM and found that they are weak, which explains the prominent nucleolar localization of wild-type NPM. Thus, the opposing balance of forces (tryptophans and NES) seems to determine the subcellular localization of NPM. The fact that W288-retaining mutants always combine with the strongest NES reveals mutational selective pressure toward efficient export into cytoplasm, pointing to this event as critical for leukemogenesis.

摘要

在急性髓性白血病(AML)中,核磷蛋白(NPM)的COOH末端核输出信号(NES)基序的产生以及色氨酸(W)288和290(或仅290)的缺失对于携带NPM1突变的NPM异常细胞质积累都至关重要。在此,我们阐明了这些COOH末端改变如何在功能上协同作用,将NPM定位到细胞质中。使用基于Rev(1.4)的穿梭试验,我们测量了在NPM突变体中鉴定出的六个不同COOH末端NES基序的核输出效率,发现其强度存在显著差异,最强的NES基序与保留W288的NPM突变体相关。当与弱NES人工偶联时,保留W288的NPM突变体不能有效地输出到细胞质中,因为驱动突变体向核仁移动的力(W288)超过了将突变体输出到细胞质中的力(NES)。然后,我们使用这种功能试验来研究野生型NPM的生理性NH(2)-末端NES基序,发现它们很弱,这解释了野生型NPM突出的核仁定位。因此,力(色氨酸和NES)的相反平衡似乎决定了NPM的亚细胞定位。保留W288的突变体总是与最强的NES结合这一事实揭示了向细胞质高效输出的突变选择压力,表明这一事件对白血病发生至关重要。

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