Y-Box Protein-1 is a Transcriptional Regulator of BMP7

被引:4
|
作者
Wang, Shinong [1 ,2 ]
Hirschberg, Raimund [1 ,2 ]
机构
[1] Harbor UCLA Med Ctr, Los Angeles Biomed Res Inst, Torrance, CA 90509 USA
[2] Univ Calif Los Angeles, Torrance, CA USA
基金
美国国家卫生研究院;
关键词
BMP7; FIBROGENESIS; TRANSCRIPTIONAL ACTIVATION; DIABETIC NEPHROPATHY; TGF beta; BONE MORPHOGENETIC PROTEIN-7; DIABETIC-NEPHROPATHY; GENE-EXPRESSION; STATISTICAL-MODEL; MESANGIAL CELLS; RETINOIC ACID; MESSENGER-RNA; YB-1; BINDING; FIBROGENESIS;
D O I
10.1002/jcb.23027
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bone morphogenetic protein-7 (BMP7) is an endogenous antifibrogenic protein in the kidney which is down regulated in experimental chronic kidney diseases such as obstructive and diabetic nephropathy in parallel with progressively increasing TGF beta. In vitro studies were performed in Madin-Darby Canine Kidney (MDCK)-cells to identify transcriptional regulators of BMP7. Experiments with various BMP7 promoter fragments (465-4,267 bp) identify small proximal promoter segments that are transcriptionally activated by high glucose (3.2-fold) but down regulated by TGF beta (0.2-fold) compared to normal glucose. Protein binding to these DNA segments is increased by high glucose and decreased by TGF beta in a time-dependent, progressive manner. Analysis of BMP7 promoter-binding proteins with liquid chromatography/tandem mass spectrometry (LC/MS/MS) identifies seven unique, partially overlapping peptides, spanning 25% of the amino acid sequence of Y-box protein-1 (YB1). EMSA-Western blot combination experiments confirm that YB1 is a BMP7 promoter-binding protein. YB1 knock-down reduces transcriptional responses to high glucose and TGF beta by about one-half, respectively. In addition, high glucose induces but TGF beta reduces nuclear translocation of YB1 from the cytoplasm. These studies identify YB1 as a transcriptional activator of BMP7 and helps to explain the progressive decline in renal BMP7 in diabetic nephropathy and other kidney diseases. J. Cell. Biochem. 112: 1130-1137, 2011. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:1130 / 1137
页数:8
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