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Cited by 211

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Molecular Cloning of a New Interferon-induced Factor That Represses Human Immunodeficiency Virus Type 1 Long Terminal Repeat Expression

Open access
Tissot, Catherine, Mechti, Nadir·1995·Journal of Biological Chemistry

Abstract

Transcriptional induction of genes is an essential part of the cellular response to interferons. To isolate yet unidentified IFN-regulated genes we have performed a differential screening on a cDNA library prepared from human lymphoblastoid Daudi cells treated for 16 h with human alpha/beta interferon (Hu-alpha/beta IFN). In the course of these studies we have isolated a human cDNA which codes for a protein sharing homology with the mouse Rpt-1 gene; it will be referred as Staf-50 for Stimulated Trans-Acting Factor of 50 kDa. Amino acid sequence analysis revealed that Staf-50 is a member of the Ring finger family and contains all the features of a transcriptional regulator able to initiate a second cascade of gene induction (secondary response). Staf-50 is induced by both type I and type II IFN in various cell lines and down-regulates the transcription directed by the long terminal repeat promoter region of human immunodeficiency virus type 1 in transfected cells. These data are consistent with a role of Staf-50 in the mechanism of transduction of the IFN antiviral action.

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Metadata

Authors
Tissot, C., & Mechti, N.
Venue
Journal of Biological Chemistry
Publisher
Elsevier BV
Published
1995-06
Volume
270
Issue
25
Pages
14891-14898
ISSN
0021-9258 (ISSN-L)
OpenAlex
W2089852194
Cited by
211
References
1
FWCI
2.91
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Molecular Cloning of a New Interferon-induced Factor That Represses Human Immunodeficiency Virus Type 1 Long Terminal Repeat Expression. https://app.cochat.ai/papers/10.1074/jbc.270.25.14891
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Tissot, C., & Mechti, N. (1995). Molecular Cloning of a New Interferon-induced Factor That Represses Human Immunodeficiency Virus Type 1 Long Terminal Repeat Expression. Journal of Biological Chemistry. https://doi.org/10.1074/jbc.270.25.14891

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