Department of Biochemistry, Boston University Medical School, Boston, MA 02118, USA.
J Cell Sci. 2012 Jun 1;125(Pt 11):2665-74. doi: 10.1242/jcs.098954. Epub 2012 Feb 22.
Aggresome formation is initiated upon proteasome failure, and facilitates autophagic clearance of protein aggregates to protect cells from proteotoxicity. Here we demonstrate that proteasome inhibition generates a signaling event to trigger aggresome formation. In aggresome signaling, the cell senses a build-up of aberrant newly synthesized proteins. The translation elongation factor eEF1A associated with these species, and knockdown of this factor suppressed aggresome formation. We used the Legionella toxin SidI to distinguish between the function of eEF1A in translation and its novel function in the aggresome formation. In fact, although it strongly inhibited translation, this toxin had only a marginal effect on aggresome formation. Furthermore, SidI reduced the threshold of the aberrant ribosomal products for triggering aggresome formation. Therefore, eEF1A binds defective polypeptides released from ribosomes, which generates a signal that triggers aggresome formation.
当蛋白酶体失能时,聚集物开始形成,并促进自噬清除蛋白聚集物以保护细胞免受毒性蛋白的侵害。在这里,我们证明了蛋白酶体抑制会产生一种信号事件来触发聚集物的形成。在聚集物信号中,细胞感知异常新合成蛋白质的积累。与这些物质相关的翻译延伸因子 eEF1A,并且该因子的敲低抑制了聚集物的形成。我们使用军团菌毒素 SidI 来区分 eEF1A 在翻译中的功能及其在聚集物形成中的新功能。事实上,尽管它强烈抑制翻译,但这种毒素对聚集物的形成只有很小的影响。此外,SidI 降低了触发聚集物形成的异常核糖体产物的阈值。因此,eEF1A 结合从核糖体释放的缺陷多肽,产生触发聚集物形成的信号。