Cato Laura, Neeb Antje, Brown Myles, Cato Andrew C B
Division of Molecular and Cellular Oncology, Department of Medical Oncology and Center for Functional Cancer Epigenetics, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02215, USA (LC, MB) and Institute of Toxicology and Genetics, Karlsruhe Institute of Technology, 76344 Eggenstein-Leopoldshafen, Germany (AN, ACBC).
Nucl Recept Signal. 2014 Nov 4;12:e005. doi: 10.1621/nrs.12005. eCollection 2014.
Molecular chaperones encompass a group of unrelated proteins that facilitate the correct assembly and disassembly of other macromolecular structures, which they themselves do not remain a part of. They associate with a large and diverse set of coregulators termed cochaperones that regulate their function and specificity. Amongst others, chaperones and cochaperones regulate the activity of several signaling molecules including steroid receptors, which upon ligand binding interact with discrete nucleotide sequences within the nucleus to control the expression of diverse physiological and developmental genes. Molecular chaperones and cochaperones are typically known to provide the correct conformation for ligand binding by the steroid receptors. While this contribution is widely accepted, recent studies have reported that they further modulate steroid receptor action outside ligand binding. They are thought to contribute to receptor turnover, transport of the receptor to different subcellular localizations, recycling of the receptor on chromatin and even stabilization of the DNA-binding properties of the receptor. In addition to these combined effects with molecular chaperones, cochaperones are reported to have additional functions that are independent of molecular chaperones. Some of these functions also impact on steroid receptor action. Two well-studied examples are the cochaperones p23 and Bag-1L, which have been identified as modulators of steroid receptor activity in nuclei. Understanding details of their regulatory action will provide new therapeutic opportunities of controlling steroid receptor action independent of the widespread effects of molecular chaperones.
分子伴侣包括一组不相关的蛋白质,它们促进其他大分子结构的正确组装和拆卸,而它们自身并不成为这些结构的一部分。它们与一大类多样的称为辅助分子伴侣的共调节因子相关联,这些共调节因子调节它们的功能和特异性。其中,分子伴侣和辅助分子伴侣调节包括类固醇受体在内的几种信号分子的活性,类固醇受体在配体结合后与细胞核内的离散核苷酸序列相互作用,以控制多种生理和发育基因的表达。通常已知分子伴侣和辅助分子伴侣为类固醇受体的配体结合提供正确的构象。虽然这一作用已被广泛接受,但最近的研究报告称,它们在配体结合之外进一步调节类固醇受体的作用。它们被认为有助于受体周转、将受体转运到不同的亚细胞定位、使受体在染色质上循环利用,甚至稳定受体的DNA结合特性。除了与分子伴侣的这些联合作用外,据报道辅助分子伴侣还具有独立于分子伴侣的其他功能。其中一些功能也影响类固醇受体的作用。两个经过充分研究的例子是辅助分子伴侣p23和Bag-1L,它们已被确定为细胞核中类固醇受体活性的调节剂。了解它们调节作用的细节将为独立于分子伴侣广泛作用来控制类固醇受体作用提供新的治疗机会。