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U2 snRNP特异性U2B''蛋白的核转运由直接和间接信号机制介导。

Nuclear transport of the U2 snRNP-specific U2B'' protein is mediated by both direct and indirect signalling mechanisms.

作者信息

Kambach C, Mattaj I W

机构信息

European Molecular Biology Laboratory, Heidelberg, Germany.

出版信息

J Cell Sci. 1994 Jul;107 ( Pt 7):1807-16. doi: 10.1242/jcs.107.7.1807.

Abstract

Experiments investigating the nuclear import of the U2 snRNP-specific B'' protein (U2B'') are presented. U2B'' nuclear transport is shown to be able to occur independently of binding to U2 snRNA. The central segment of the protein (amino acids 90-146) encodes an unusual nuclear localization signal (NLS) that is related to that of the U1 snRNP-specific A protein. However, nuclear import of U2B'' does not depend on this NLS. Sequences in the N-terminal RNP motif of the protein are sufficient to direct nuclear transport, and evidence is presented that the interaction of U2B'' with the U2A' protein mediates this effect. This suggests that U2B'' can 'piggy-back' to the nucleus in association with U2A', and thus be imported to the nucleus by two different mechanisms. U2A' nuclear transport, on the other hand, can occur independently of both U2B'' binding and of U2 snRNA.

摘要

本文展示了对U2 snRNP特异性B''蛋白(U2B'')核输入的研究实验。研究表明,U2B''的核转运能够独立于与U2 snRNA的结合而发生。该蛋白的中央区段(氨基酸90 - 146)编码一种不同寻常的核定位信号(NLS),它与U1 snRNP特异性A蛋白的核定位信号相关。然而,U2B''的核输入并不依赖于这个NLS。该蛋白N端RNP基序中的序列足以指导核转运,并且有证据表明U2B''与U2A'蛋白的相互作用介导了这一效应。这表明U2B''可以与U2A'一起“搭便车”进入细胞核,从而通过两种不同机制被导入细胞核。另一方面,U2A'的核转运可以独立于U2B''结合和U2 snRNA而发生。

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