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Volume 272, Number 31, Issue of August 1, 1997 pp. 19457-19463
©1997 by The American Society for Biochemistry and Molecular Biology, Inc.

Molecular Cloning of a New Interferon-induced PML Nuclear Body-associated Protein

(Received for publication, April 1, 1997, and in revised form, May 8, 1997)

Celine Gongora Dagger , Gregory David § , Lionel Pintard Dagger , Catherine Tissot Dagger , The Duc Hua Dagger , Anne Dejean § and Nadir Mechti Dagger

From the Dagger  Institut de Genetique Moleculaire de Montpellier-UMR 9942, CNRS, 34033 Montpellier Cedex 1 and the § Unité de Recombinaison et Expression Génétique, INSERM U163, Institut Pasteur, 75724 Paris Cedex 15, France

Transcriptional induction of genes is an essential part of the cellular response to interferons. We have established a cDNA library from human lymphoblastoid Daudi cells treated for 16 h with human alpha /beta -interferon (IFN) and made use of differential screening to search for as yet unidentified IFN-regulated genes. In the course of this study, we have isolated a human cDNA that codes for a 20-kDa protein sharing striking homology with the product of the Xenopus laevis XPMC2 gene. This new gene is induced by both type I and II IFNs in various cell lines and will be referred to as ISG20 for interferon-stimulated gene product of 20 kDa. Confocal immunofluorescence analysis of the subcellular localization of ISG20 protein reveals that it is closely associated with PML and SP100 gene products within the large nuclear matrix-associated multiprotein complexes termed the PML nuclear bodies.


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