کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1930532 1050517 2011 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
BRG1 is indispensable for IFN-γ-induced TRIM22 expression, which is dependent on the recruitment of IRF-1
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
BRG1 is indispensable for IFN-γ-induced TRIM22 expression, which is dependent on the recruitment of IRF-1
چکیده انگلیسی

The modification of chromatin structure is increasingly recognized to be an important facet of transcriptional regulation. Here, we report that Brahma-related gene 1 (BRG1), a chromatin remodeling enzyme, plays a crucial role in IFN-γ-induced TRIM22 expression. Our results showed that IFN-γ failed to induce TRIM22 expression in BRG1-deficient SW-13 cells, and reconstitution of BRG1 in this cell line could restore IFN-γ induction of TRIM22. Furthermore, it was revealed that BRG1 absence, per se, did not impair IFN-γ-induced IRF-1 expression, but blocked its access to TRIM22 promoter, and BRG1-dependent induction of TRIM22 perfectly correlated with BRG1-dependent recruitment of IRF-1 to TRIM22 promoter. We also found that the DNA-dependent ATPase domain of BRG1 was required for TRIM22 expression and IRF-1 recruitment in response to IFN-γ stimulation, suggesting that BRG1-mediated chromatin remodeling is critical for the IFN-γ-inducibility of TRIM22 gene.


► IFN-γ fails to induce TRIM22 in BRG1-deficient SW-13 cells.
► Expression of BRG1 rescues IFN-γ induction of TRIM22 in SW-13 cells.
► BRG1 absence does not impair IFN-γ-induced IRF-1 expression and its binding activity, but blocks its recruitment to TRIM22 promoter.
► BRG1-dependent induction of TRIM22 correlates perfectly with BRG1-dependent recruitment of IRF-1 to TRIM22 promoter.
► DNA-dependent ATPase domain of BRG1 is required for TRIM22 expression and IRF-1 recruitment in response to IFN-γ stimulation.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochemical and Biophysical Research Communications - Volume 410, Issue 3, 8 July 2011, Pages 549–554
نویسندگان
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