Itatani Yoshiro, Sonoshita Masahiro, Kakizaki Fumihiko, Okawa Katsuya, Stifani Stefano, Itoh Hideaki, Sakai Yoshiharu, Taketo M Mark
Department of Pharmacology and Department of Surgery, Graduate School of Medicine, Kyoto University, Yoshida Konoé-cho, Sakyo-ku, Kyoto 606-8501, Japan;
Department of Pharmacology and.
J Biochem. 2016 Jan;159(1):133-40. doi: 10.1093/jb/mvv077. Epub 2015 Jul 29.
Amino-terminal enhancer of split (Aes) is a member of Groucho/Transducin-like enhancer (TLE) family. Aes is a recently found metastasis suppressor of colorectal cancer (CRC) that inhibits Notch signalling, and forms nuclear foci together with TLE1. Although some Notch-associated proteins are known to form subnuclear bodies, little is known regarding the dynamics or functions of these structures. Here, we show that Aes nuclear foci in CRC observed under an electron microscope are in a rather amorphous structure, lacking surrounding membrane. Investigation of their behaviour during the cell cycle by time-lapse cinematography showed that Aes nuclear foci dissolve during mitosis and reassemble after completion of cytokinesis. We have also found that heat shock cognate 70 (HSC70) is an essential component of Aes foci. Pharmacological inhibition of the HSC70 ATPase activity with VER155008 reduces Aes focus formation. These results provide insight into the understanding of Aes-mediated inhibition of Notch signalling.
分裂蛋白氨基末端增强子(Aes)是Groucho/转导素样增强子(TLE)家族的成员。Aes是最近发现的一种抑制Notch信号传导的结直肠癌(CRC)转移抑制因子,它与TLE1一起形成核灶。尽管已知一些与Notch相关的蛋白质会形成亚核小体,但对于这些结构的动态变化或功能却知之甚少。在这里,我们发现,在电子显微镜下观察到的CRC中的Aes核灶呈相当无定形的结构,没有周围的膜。通过延时摄影对其在细胞周期中的行为进行研究表明,Aes核灶在有丝分裂期间溶解,并在胞质分裂完成后重新组装。我们还发现,热休克同源蛋白70(HSC70)是Aes核灶的一个重要组成部分。用VER155008对HSC70 ATP酶活性进行药理学抑制会减少Aes核灶的形成。这些结果为理解Aes介导的对Notch信号传导的抑制提供了线索。