Supplementary Materials for:
Inhibition of PP1 Phosphatase Activity by HBx: A Mechanism for the
Activation of Hepatitis B Virus Transcription
Delphine Cougot, Eric Allemand, Lise Rivière, Shirine Benhenda, Karine Duroure,
Florence Levillayer, Christian Muchardt, Marie-Annick Buendia, Christine Neuveut*
*To whom correspondence should be addressed. E-mail: christine.neuveut{at}pasteur.fr
This PDF file includes:
- Fig. S1. Analysis of integrated HBV DNA and cccDNA in HepAD38 cells.
- Fig. S2. Role of CREB in HBV DNA transcription.
- Fig. S3. HBx prolongs CREB phosphorylation in HepG2 cells.
- Fig. S4. HBx interacts with PP1 and HDAC1.
- Fig. S5. Endogenous PP1 elutes with HDAC1 and HA-HBx in high–molecular
weight fractions.
- Fig. S6. The C-terminal region of HBx interacts with PP1 and is required for
prolongation of CREB phosphorylation.
- Fig. S7. Analysis of His-PP1α elution and HA-HBx abundance by Western blot.
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Citation: D. Cougot, E. Allemand, L. Rivière, S. Benhenda, K. Duroure, F. Levillayer,
C. Muchardt, M.-A. Buendia, C. Neuveut, Inhibition of PP1 Phosphatase Activity by HBx: A Mechanism for the
Activation of Hepatitis B Virus Transcription.
Sci.
Signal. 5, ra1 (2012).
© 2012 American Association for the Advancement of Science