Previous Article | Next Article ![]()
Journal of Virology, November 2001, p. 10779-10786, Vol. 75, No. 22
Department of Pathology, VA Medical Center
113B, University of California School of Medicine, San Francisco,
California 94121,1 and Department of
Molecular Microbiology and Immunology, Howard Hughes Medical Institute,
Keck School of Medicine, University of Southern California, Los
Angeles, California 900332
Received 18 April 2001/Accepted 7 August 2001
The hepatitis B virus posttranscriptional regulatory element (PRE)
is an RNA element that increases the expression of unspliced mRNAs,
apparently by facilitating their export from the nucleus. We have
identified a cellular protein that binds to the PRE as the
polypyrimidine tract binding protein (PTB), which shuttles rapidly
between the nucleus and the cytoplasm. Mutants of the PRE with
mutations in PTB binding sites show markedly decreased activity, while
cells that stably overexpress PTB show increased PRE-dependent gene
expression. Export of PTB from the nucleus, like PRE function, is
blocked by a mutant form of Ran binding protein 1 but not by leptomycin
B. Therefore, PTB is important for PRE activity and appears to function
as an export factor for PRE-containing mRNAs.
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.22.10779-10786.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Role of Polypyrimidine Tract Binding Protein in the
Function of the Hepatitis B Virus Posttranscriptional Regulatory
Element
*
Corresponding author. Mailing address: Department of
Pathology, VA Medical Center 113B, University of California School of Medicine, 4150 Clement St., San Francisco, CA 94121. Phone: (415) 476-6006. Fax: (415) 750-6947. E-mail:
yen{at}itsa.ucsf.edu.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»