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核转运蛋白Kap142p/Msn5p介导不同货物蛋白的核输入和核输出。

The karyopherin Kap142p/Msn5p mediates nuclear import and nuclear export of different cargo proteins.

作者信息

Yoshida K, Blobel G

机构信息

Laboratory of Cell Biology, Howard Hughes Medical Institute, The Rockefeller University, New York, New York 10021, USA.

出版信息

J Cell Biol. 2001 Feb 19;152(4):729-40. doi: 10.1083/jcb.152.4.729.

Abstract

We have identified a novel pathway for protein import into the nucleus. Although the product of Saccharomyces cerevisiae gene MSN5 was previously shown to function as a karyopherin (Kap) for nuclear export of various proteins, we discovered a nuclear import pathway mediated by Msn5p (also referred to as Kap142p). We have purified from yeast cytosol a complex containing Kap142p and the trimeric replication protein A (RPA), which is required for multiple aspects of DNA metabolism, including DNA replication, DNA repair, and recombination. In wild-type cells, RPA was localized primarily to the nucleus but, in a KAP142 deletion strain, RPA was mislocalized to the cytoplasm and the strain was highly sensitive to bleomycin (BLM). BLM causes DNA double-strand breaks and, in S. cerevisiae, the DNA damage is repaired predominantly by RPA-dependent homologous recombination. Therefore, our results indicate that in wild-type cells a critical portion of RPA was imported into the nucleus by Kap142p. Like several other import-related Kap-substrate complexes, the endogenous RPA-Kap142p complex was dissociated by RanGTP, but not by RanGDP. All three RPA genes are essential for viability, whereas KAP142 is not. Perhaps explaining this disparity, we observed an interaction between RPA and Kap95p in a strain lacking Kap142p. This interaction could provide a mechanism for import of RPA into the nucleus and cell viability in the absence of Kap142p. Together with published results (Kaffman, A., N.M. Rank, E.M. O'Neill, L.S. Huang, and E.K. O'Shea. 1998. Nature. 396:482-486; Blondel, M., P.M. Alepuz, L.S. Huang, S. Shaham, G. Ammerer, and M. Peter. 1999. Genes Dev. 13:2284-2300; DeVit, M.J., and M. Johnston. 1999. Curr. Biol. 9:1231-1241; Mahanty, S.K., Y. Wang, F.W. Farley, and E.A. Elion. 1999. Cell. 98:501-512) our data indicate that the karyopherin Kap142p is able to mediate nuclear import of one set of proteins and nuclear export of a different set of proteins.

摘要

我们已经确定了一种蛋白质导入细胞核的新途径。尽管酿酒酵母基因MSN5的产物先前已被证明作为多种蛋白质核输出的核转运蛋白(核转运受体,Kap)发挥作用,但我们发现了一种由Msn5p(也称为Kap142p)介导的核输入途径。我们从酵母细胞质中纯化了一种包含Kap142p和三聚体复制蛋白A(RPA)的复合物,RPA参与DNA代谢的多个方面,包括DNA复制、DNA修复和重组。在野生型细胞中,RPA主要定位于细胞核,但在KAP142缺失菌株中,RPA错误定位于细胞质,并且该菌株对博来霉素(BLM)高度敏感。BLM会导致DNA双链断裂,在酿酒酵母中,DNA损伤主要通过RPA依赖的同源重组进行修复。因此,我们的结果表明,在野生型细胞中,RPA的关键部分由Kap142p导入细胞核。与其他几种与输入相关的Kap-底物复合物一样,内源性RPA-Kap142p复合物被RanGTP解离,但不被RanGDP解离。所有三个RPA基因对于细胞存活都是必需的,而KAP142则不是。也许可以解释这种差异的是,我们在缺乏Kap142p的菌株中观察到RPA与Kap95p之间存在相互作用。这种相互作用可以为在没有Kap142p的情况下RPA导入细胞核和细胞存活提供一种机制。结合已发表的结果(Kaffman, A., N.M. Rank, E.M. O'Neill, L.S. Huang, and E.K. O'Shea. 1998. Nature. 396:482 - 486; Blondel, M., P.M. Alepuz, L.S. Huang, S. Shaham, G. Ammerer, and M. Peter. 1999. Genes Dev. 13:2284 - 2300; DeVit, M.J., and M. Johnston. 1999. Curr. Biol. 9:1231 - 1241; Mahanty, S.K., Y. Wang, F.W. Farley, and E.A. Elion. 1999. Cell. 98:501 - 512),我们的数据表明核转运受体Kap142p能够介导一组蛋白质的核输入和另一组蛋白质的核输出。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/647f/2195777/7e9bb8d96d2f/JCB0004072.f1.jpg

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