| Literature DB >> 24413774 |
Andreas Begitt1, Mathias Droescher2, Thomas Meyer3, Christoph D Schmid4, Michelle Baker5, Filipa Antunes1, Klaus-Peter Knobeloch, Markus R Owen5, Ronald Naumann6, Thomas Decker7, Uwe Vinkemeier8.
Abstract
STAT1 is an indispensable component of a heterotrimer (ISGF3) and a STAT1 homodimer (GAF) that function as transcription regulators in type 1 and type 2 interferon signaling, respectively. To investigate the importance of STAT1-cooperative DNA binding, we generated gene-targeted mice expressing cooperativity-deficient STAT1 with alanine substituted for Phe77. Neither ISGF3 nor GAF bound DNA cooperatively in the STAT1F77A mouse strain, but type 1 and type 2 interferon responses were affected differently. Type 2 interferon-mediated transcription and antibacterial immunity essentially disappeared owing to defective promoter recruitment of GAF. In contrast, STAT1 recruitment to ISGF3 binding sites and type 1 interferon-dependent responses, including antiviral protection, remained intact. We conclude that STAT1 cooperativity is essential for its biological activity and underlies the cellular responses to type 2, but not type 1 interferon.Entities:
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Year: 2014 PMID: 24413774 DOI: 10.1038/ni.2794
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 25.606