کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2195670 1550865 2015 11 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Yin Yang 1 is a multi-functional regulator of adipocyte differentiation in 3T3-L1 cells
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیولوژی سلول
پیش نمایش صفحه اول مقاله
Yin Yang 1 is a multi-functional regulator of adipocyte differentiation in 3T3-L1 cells
چکیده انگلیسی


• YY1 gene and protein expression was transiently downregulated upon the induction of differentiation.
• YY1 overexpression decreased adipocyte differentiation and blocked cell differentiation at the preadipocyte stage.
• YY1 physically interacted with PPARγ and C/EBPβ respectively.
• YY1 directly decreased PPARγ transcriptional activity.

Yin Yang 1 (YY1) is an ubiquitously distributed transcription factor that belongs to the GLI-Kruppel class of zinc finger proteins. The mechanism by which YY1 regulates adipocyte differentiation remains unclear. In this study, we investigated the functional role of YY1 during adipocyte differentiation. During the early stage, YY1 gene and protein expression was transiently downregulated upon the induction of differentiation, however, it was consistently induced during the later stage. YY1 overexpression decreased adipocyte differentiation and blocked cell differentiation at the preadipocyte stage, while YY1 knockdown by RNA interference increased adipocyte differentiation. YY1 physically interacted with PPARγ (Peroxisome proliferator-activated receptor gamma) and C/EBPβ (CCAAT/enhancer-binding protein beta) respectively in 3T3-L1 cells. Through its interaction with PPARγ, YY1 directly decreased PPARγ transcriptional activity. YY1 ectopic expression prevented C/EBPβ from binding to the PPARγ promoter, resulting in the downregulation of PPARγ transcriptional activity. These results indicate that YY1 repressed adipocyte differentiation by repressing the activity of adipogenic transcriptional factors in 3T3-L1 cells.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Molecular and Cellular Endocrinology - Volume 413, 15 September 2015, Pages 217–227
نویسندگان
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