Yasuda Kunihiko, Ohyama Kyoji, Onga Kazuko, Kakizuka Akira, Mori Nozomu
From the Department of Anatomy and Neurobiology, Nagasaki University School of Medicine, Nagasaki, Japan.
Laboratory of Functional Biology, Kyoto University Graduate School of Biostudies, Kyoto, Japan.
PLoS One. 2013 Dec 16;8(12):e82523. doi: 10.1371/journal.pone.0082523. eCollection 2013.
Mdm20 is an auxiliary subunit of the NatB complex, which includes Nat5, the catalytic subunit for protein N-terminal acetylation. The NatB complex catalyzes N-acetylation during de novo protein synthesis initiation; however, recent evidence from yeast suggests that NatB also affects post-translational modification of tropomyosin, which is involved in intracellular sorting of aggregated proteins. We hypothesized that an acetylation complex such as NatB may contribute to protein clearance and/or proteostasis in mammalian cells. Using a poly glutamine (polyQ) aggregation system, we examined whether the NatB complex or its components affect protein aggregation in rat primary cultured hippocampal neurons and HEK293 cells. The number of polyQ aggregates increased in Mdm20 over-expressing (OE) cells, but not in Nat5-OE cells. Conversely, in Mdm20 knockdown (KD) cells, but not in Nat5-KD cells, polyQ aggregation was significantly reduced. Although Mdm20 directly associates with Nat5, the overall cellular localization of the two proteins was slightly distinct, and Mdm20 apparently co-localized with the polyQ aggregates. Furthermore, in Mdm20-KD cells, a punctate appearance of LC3 was evident, suggesting the induction of autophagy. Consistent with this notion, phosphorylation of Akt, most notably at Ser473, was greatly reduced in Mdm20-KD cells. These results demonstrate that Mdm20, the so-called auxiliary subunit of the translation-coupled protein N-acetylation complex, contributes to protein clearance and/or aggregate formation by affecting the phosphorylation level of Akt indepenently from the function of Nat5.
Mdm20是NatB复合物的一个辅助亚基,NatB复合物包括Nat5,它是蛋白质N端乙酰化的催化亚基。NatB复合物在新生蛋白质合成起始过程中催化N-乙酰化;然而,来自酵母的最新证据表明,NatB也影响原肌球蛋白的翻译后修饰,原肌球蛋白参与聚集蛋白的细胞内分选。我们推测,像NatB这样的乙酰化复合物可能有助于哺乳动物细胞中的蛋白质清除和/或蛋白质稳态。使用聚谷氨酰胺(polyQ)聚集系统,我们研究了NatB复合物或其组分是否影响大鼠原代培养海马神经元和HEK293细胞中的蛋白质聚集。在过表达(OE)Mdm20的细胞中聚Q聚集体的数量增加,但在过表达Nat5的细胞中没有增加。相反,在敲低(KD)Mdm20的细胞中,而不是在敲低Nat5的细胞中,聚Q聚集显著减少。尽管Mdm20直接与Nat5相关联,但这两种蛋白质的整体细胞定位略有不同,并且Mdm20明显与聚Q聚集体共定位。此外,在敲低Mdm20的细胞中,LC3呈现点状外观,表明自噬被诱导。与此观点一致,在敲低Mdm20的细胞中,Akt的磷酸化,最显著的是在Ser473处,大大降低。这些结果表明,翻译偶联蛋白N-乙酰化复合物的所谓辅助亚基Mdm20,通过独立于Nat5的功能影响Akt的磷酸化水平,从而有助于蛋白质清除和/或聚集体形成。