| Literature DB >> 26229111 |
Yoshiro Itatani1, Masahiro Sonoshita2, Fumihiko Kakizaki2, Katsuya Okawa3, Stefano Stifani4, Hideaki Itoh5, Yoshiharu Sakai6, M Mark Taketo7.
Abstract
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.Entities:
Keywords: Notch signalling; colorectal cancer; heat shock protein; nuclear matrix; transcription
Mesh:
Substances:
Year: 2015 PMID: 26229111 PMCID: PMC4882644 DOI: 10.1093/jb/mvv077
Source DB: PubMed Journal: J Biochem ISSN: 0021-924X Impact factor: 3.387