Np95 is a histone-binding protein endowed with ubiquitin ligase activity.
Np95 is an important determinant in cell cycle progression. Its expression is tightly regulated and becomes detectable shortly before the entry of cells into S phase. Accordingly, Np95 is absolutely required for the G1/S transition. Its continued expression throughout the S/G2/M phases further suggests additional roles. Indeed, Np95 has been implicated in DNA damage response. Here, we show that Np95 is tightly bound to chromatin in vivo and that it binds to histones in vivo and in vitro. The binding to histones is direct and shows a remarkable preference for histone H3 and its N-terminal tail. A novel protein domain, the SRA-YDG domain, contained in Np95 is indispensable both for the interaction with histones and for chromatin binding in vivo. Np95 contains a RING finger. We show that this domain confers E3 ubiquitin ligase activity on Np95, which is specific for core histones, in vitro. Finally, Np95 shows specific E3 activity for histone H3 when the endogenous core octamer, coimmunoprecipitating with Np95, is used as a substrate. Histone ubiquitination is an important determinant in the regulation of chromatin structure and gene transcription. Thus, the demonstration that Np95 is a chromatin-associated ubiquitin ligase suggests possible molecular mechanisms for its action as a cell cycle regulator.
Pubmed ID: 14993289 RIS Download
Amino Acid Sequence | Animals | Binding Sites | Carrier Proteins | Cattle | Cell Line | Chromatin | Chromosomal Proteins, Non-Histone | Humans | In Vitro Techniques | Mice | Molecular Sequence Data | NIH 3T3 Cells | Nuclear Proteins | Protein Structure, Tertiary | Recombinant Proteins | Sequence Homology, Amino Acid | Ubiquitin-Protein Ligases