Hong Wei, Baniahmad Aria, Liu Yunde, Li Huiqiang
Department of Laboratory Medicine, Tianjin Medical University, 300203 Tianjin, China.
J Mol Biol. 2008 Dec 5;384(1):22-30. doi: 10.1016/j.jmb.2008.09.010. Epub 2008 Sep 16.
Molecular chaperones and cochaperones are known to participate in nuclear receptor-mediated gene expression in addition to providing the appropriate conformation for hormone binding. It has been reported that Bag-1M (Bcl-2 associated athanogene 1M) downregulates the transactivation function of the glucocorticoid receptor (GR). Here, we demonstrate that Bag-1M downregulates the glucocorticoid function via binding to distinct amino acid sequences in the hinge region of the GR. In cells expressing the human metallothionein IIa gene, overexpression of Bag-1M resulted in an in vivo dissociation of the DNA-receptor complex and a decrease in glucocorticoid-mediated transcription, indicating that this cochaperone acts as a negative regulator of GR action. In Bag-1M-expressing cells, this cochaperone is recruited with the GR to genomic hormone response element following glucocorticoid treatment. In line with this, small interfering RNA knockdown of the cellular level of Bag-1M enhanced DNA binding by the GR, resulting in a robust increase in transcriptional activity. These findings identify a regulatory mechanism, downstream of hormone binding, used by Bag-1M for attenuating GR action in response to its changing cellular levels.
分子伴侣和辅助分子伴侣除了为激素结合提供合适的构象外,还参与核受体介导的基因表达。据报道,Bag-1M(Bcl-2相关抗凋亡基因1M)下调糖皮质激素受体(GR)的反式激活功能。在此,我们证明Bag-1M通过与GR铰链区不同的氨基酸序列结合来下调糖皮质激素功能。在表达人金属硫蛋白IIa基因的细胞中,Bag-1M的过表达导致DNA-受体复合物在体内解离,并降低糖皮质激素介导的转录,表明这种辅助分子伴侣作为GR作用的负调节因子。在表达Bag-1M的细胞中,糖皮质激素处理后,这种辅助分子伴侣与GR一起被募集到基因组激素反应元件上。与此一致的是,通过小干扰RNA敲低细胞中Bag-1M的水平可增强GR与DNA的结合,导致转录活性显著增加。这些发现确定了一种在激素结合下游的调节机制,Bag-1M利用该机制根据其细胞水平的变化来减弱GR的作用。