کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1930580 1050518 2011 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Histone chaperones cooperate to mediate Mef2-targeted transcriptional regulation during skeletal myogenesis
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
Histone chaperones cooperate to mediate Mef2-targeted transcriptional regulation during skeletal myogenesis
چکیده انگلیسی

Histone chaperones function in histone transfer and regulate the nucleosome occupancy and the activity of genes. HIRA is a replication-independent (RI) histone chaperone that is linked to transcription and various developmental processes. Here, we show that HIRA interacts with Mef2 and contributes to the activation of Mef2-target genes during muscle differentiation. Asf1 cooperated with HIRA and was indispensable for Mef2-dependent transcription. The HIRA R460A mutant, which is defective in Asf1 binding, lost the transcriptional co-activation. In addition, the role of Cabin1, previously reported as a Mef2 repressor and as one of the components of the HIRA-containing complex, was delineated in Mef2/HIRA-mediated transcription. Cabin1 associated with the C-terminus of HIRA via its N-terminal domain and suppressed Mef2/HIRA-mediated transcription. Expression of Cabin1 was dramatically reduced upon myoblast differentiation, which may allow Mef2 and HIRA/Asf1 to resume their transcriptional activity. HIRA led to more permeable chromatin structure marked by active histone modifications around the myogenin promoter. Our results suggest that histone chaperone complex components contribute to the regulation of Mef2 target genes for muscle differentiation.


► HIRA participates in Mef2-mediated transcriptional activation.
► Domain analysis of HIRA as a coactivator of Mef2.
► Asf1 cooperates with HIRA for coactivation of Mef2-dependent transcription.
► Cabin1 interacts with HIRA and counteracts the transcriptional activity of Mef2.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochemical and Biophysical Research Communications - Volume 407, Issue 3, 15 April 2011, Pages 541–547
نویسندگان
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