The BioGRID | PUBLICATION VIEW

	Biochem. Biophys. Res. Commun. Sep (2001); 286(5):886-94
Through induction of juxtaposition and tyrosine kinase activity of Jak1, X-gene product of hepatitis B virus stimulates Ras and the transcriptional activation through AP-1, NF-kappaB, and SRE enhancers.
Kim H, Lee YH, Won J, Yun Y
Division of Molecular Life Science and Center for Cell Signaling Research, Ewha Woman's University, 11-1 Daehyundong, Seoul, Seodaemoongu, 120-750, Korea.
Abstract: Here, based on the recent finding of HBx (X-gene product of hepatitis B virus) as the inducer of Jak1, we investigated the mechanism for the HBx-mediated host cell regulation and found that (i) HBx associates specifically with Jak1 in vivo; (ii) HBx itself forms a dimer which leads to juxtaposition of associated Jak1 and subsequent activation of the tyrosine kinase activity of Jak1; (iii) HBx-mediated activation of the promoters containing AP-1-, NF-kappaB-, SRE-, and SIE-sites is dependent on the activation of Jak1; (iv) Jak1, once activated by HBx, induces Ras activity through recruitment of Grb2 and induces tyrosine phosphorylation of Raf1, but not shc. These findings show that previously reported functions of HBx, such as activation of multiple signaling pathways and transcriptional activation are attributable to HBx-mediated Jak1 activation.
[PUBMED: 11527382]