首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Two Isoforms of Npap60 (Nup50) Differentially Regulate Nuclear Protein Import
Authors:Yutaka Ogawa  Yoichi Miyamoto  Munehiro Asally  Masahiro Oka  Yoshinari Yasuda  Yoshihiro Yoneda
Institution:*Department of Frontier Biosciences, Graduate School of Frontier Biosciences, and ;Department of Biochemistry, Graduate School of Medicine, Osaka University, Suita, Osaka 565-0871, Japan; and ;JST, CREST, Suita, Osaka 565-0871, Japan
Abstract:Npap60 (Nup50) is a nucleoporin that binds directly to importin α. In humans, there are two Npap60 isoforms: the long (Npap60L) and short (Npap60S) forms. In this study, we provide both in vitro and in vivo evidence that Npap60L and Npap60S function differently in nuclear protein import. In vitro binding assays revealed that Npap60S stabilizes the binding of importin α to classical NLS-cargo, whereas Npap60L promotes the release of NLS-cargo from importin α. In vivo time-lapse experiments showed that when the Npap60 protein level is controlled, allowing CAS to efficiently promote the dissociation of the Npap60/importin α complex, Npap60S and Npap60L suppress and accelerate the nuclear import of NLS-cargo, respectively. These results demonstrate that Npap60L and Npap60S have opposing functions and suggest that Npap60L and Npap60S levels must be carefully controlled for efficient nuclear import of classical NLS-cargo in humans. This study provides novel evidence that nucleoporin expression levels regulate nuclear import efficiency.
Keywords:
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号