Linares Laëtitia K, Scheffner Martin
Center for Biochemistry, Faculty of Medicine, and Center for Molecular Medicine, University of Cologne, Joseph-Stelzmann-Str. 52, 50931 Köln, Germany.
FEBS Lett. 2003 Nov 6;554(1-2):73-6. doi: 10.1016/s0014-5793(03)01108-6.
The proto-oncoprotein Hdm2 is a member of the RING finger-type family of ubiquitin-protein ligases E3. The RING finger domain is assumed to mediate the specific interaction of an E3 with its cognate ubiquitin-conjugating enzyme E2, which catalyzes the covalent attachment of ubiquitin to substrate proteins. In addition, the RING finger domain of Hdm2 is involved in Hdm2 homooligomer formation and has the capacity to bind to RNA in a sequence-specific manner. Here we report that interaction with nucleic acids interferes with both Hdm2/Hdm2 complex formation and auto-ubiquitination of Hdm2 in vitro. Furthermore, although binding of Hdm2 to the tumor suppressor p53 is not inhibited by nucleic acids, Hdm2-mediated ubiquitination of p53 is significantly decreased. Taken together, these results provide the first example of an E3 whose activity can be regulated by direct interaction with nucleic acids.
原癌蛋白Hdm2是泛素-蛋白连接酶E3的环状结构域家族成员。环状结构域被认为介导E3与其同源泛素结合酶E2的特异性相互作用,E2催化泛素与底物蛋白的共价连接。此外,Hdm2的环状结构域参与Hdm2同源寡聚体的形成,并能够以序列特异性方式结合RNA。在此我们报告,在体外,与核酸的相互作用会干扰Hdm2/Hdm2复合物的形成以及Hdm2的自身泛素化。此外,尽管核酸不会抑制Hdm2与肿瘤抑制因子p53的结合,但Hdm2介导的p53泛素化显著减少。综上所述,这些结果提供了首个E3活性可通过与核酸直接相互作用进行调节的实例。