Tsujii Akira, Miyamoto Yoichi, Moriyama Tetsuji, Tsuchiya Yuko, Obuse Chikashi, Mizuguchi Kenji, Oka Masahiro, Yoneda Yoshihiro
From the Graduate School of Medicine and the Laboratories of Nuclear Transport Dynamics and.
the Laboratories of Nuclear Transport Dynamics and.
J Biol Chem. 2015 Dec 4;290(49):29375-88. doi: 10.1074/jbc.M115.681908. Epub 2015 Oct 21.
Nucleocytoplasmic trafficking is a fundamental cellular process in eukaryotic cells. Here, we demonstrated that retinoblastoma-binding protein 4 (RBBP4) functions as a novel regulatory factor to increase the efficiency of importin α/β-mediated nuclear import. RBBP4 accelerates the release of importin β1 from importin α via competitive binding to the importin β-binding domain of importin α in the presence of RanGTP. Therefore, it facilitates importin α/β-mediated nuclear import. We showed that the importin α/β pathway is down-regulated in replicative senescent cells, concomitant with a decrease in RBBP4 level. Knockdown of RBBP4 caused both suppression of nuclear transport and induction of cellular senescence. This is the first report to identify a factor that competes with importin β1 to bind to importin α, and it demonstrates that the loss of this factor can trigger cellular senescence.
核质运输是真核细胞中的一个基本细胞过程。在此,我们证明视网膜母细胞瘤结合蛋白4(RBBP4)作为一种新型调节因子发挥作用,可提高输入蛋白α/β介导的核输入效率。在RanGTP存在的情况下,RBBP4通过与输入蛋白α的输入蛋白β结合结构域竞争性结合,加速输入蛋白β1从输入蛋白α的释放。因此,它促进了输入蛋白α/β介导的核输入。我们发现,在复制性衰老细胞中,输入蛋白α/β途径下调,同时RBBP4水平降低。敲低RBBP4会导致核运输受抑制和细胞衰老诱导。这是首次报道鉴定出一种与输入蛋白β1竞争结合输入蛋白α的因子,并且证明该因子的缺失可触发细胞衰老。