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TMF/ARA160是一种含BC盒的蛋白质,可介导Stat3的降解。

TMF/ARA160 is a BC-box-containing protein that mediates the degradation of Stat3.

作者信息

Perry Erez, Tsruya Rachel, Levitsky Pavel, Pomp Oz, Taller Michal, Weisberg Shira, Parris Wendy, Kulkarni Sarang, Malovani Hana, Pawson Tony, Shpungin Sally, Nir Uri

机构信息

Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan 52900, Israel.

出版信息

Oncogene. 2004 Nov 25;23(55):8908-19. doi: 10.1038/sj.onc.1208149.

DOI:10.1038/sj.onc.1208149
PMID:15467733
Abstract

TMF/ARA160 is a Golgi resident protein whose cellular functions have not been conclusively revealed. Herein we show that TMF/ARA160 can direct the proteasomal degradation of the key cell growth regulator - Stat3. TMF/ARA160 was dispersed in the cytoplasm of myogenic C2C12 cells that were grown under low-serum conditions. The cytoplasmic distribution of TMF/ARA160 was accompanied by its transient association with the tyrosine kinase Fer and with Stat3, which underwent proteasomal degradation under those conditions. Moreover, serum deprivation induced the association of ubiquitinated proteins, with the TMF/ARA160 complex. However, TMF/ARA160 did not bind Stat1, whose cellular levels were increased in serum-starved C2C12 cells. Amino-acid sequence analysis identified a BC-box element in TMF/ARA160 that mediated the binding of this protein to elongin C. Ectopic expression of TMF/ARA160 in serum-starved C2C12 cells drove the ubiquitination and proteasomal degradation of Stat3, an effect that was not caused by TMF/ARA160 devoid of the BC-box motif. Thus, the Golgi apparatus harbors a novel BC-box-containing protein that can direct Stat3 to proteasomal degradation. Interestingly, the level of TMF/ARA160 was significantly decreased in malignant brain tumors, implying a suppressive role of that protein in tumor progression.

摘要

TMF/ARA160是一种驻留于高尔基体的蛋白质,其细胞功能尚未得到最终揭示。在此我们表明,TMF/ARA160可引导关键细胞生长调节因子Stat3的蛋白酶体降解。TMF/ARA160分散于在低血清条件下生长的成肌C2C12细胞的细胞质中。TMF/ARA160的细胞质分布伴随着它与酪氨酸激酶Fer以及Stat3的短暂结合,Stat3在这些条件下会经历蛋白酶体降解。此外,血清剥夺诱导泛素化蛋白与TMF/ARA160复合物结合。然而,TMF/ARA160不与Stat1结合,Stat1在血清饥饿的C2C12细胞中的细胞水平会升高。氨基酸序列分析在TMF/ARA160中鉴定出一个BC盒元件,该元件介导了这种蛋白质与延伸蛋白C的结合。在血清饥饿的C2C12细胞中异位表达TMF/ARA160会促使Stat3的泛素化和蛋白酶体降解,而缺乏BC盒基序的TMF/ARA160则不会产生这种效应。因此,高尔基体含有一种新型的含BC盒蛋白,它可引导Stat3进行蛋白酶体降解。有趣的是,TMF/ARA160的水平在恶性脑肿瘤中显著降低,这意味着该蛋白在肿瘤进展中具有抑制作用。

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