二价离子转换驱动 H-NS/DNA 结合构象在僵硬和桥连模式之间转换。
A divalent switch drives H-NS/DNA-binding conformations between stiffening and bridging modes.
机构信息
Department of Physics, National University of Singapore, Singapore 117542.
出版信息
Genes Dev. 2010 Feb 15;24(4):339-44. doi: 10.1101/gad.1883510.
Heat-stable nucleoid structuring protein (H-NS) is an abundant prokaryotic protein that plays important roles in organizing chromosomal DNA and gene silencing. Two controversial binding modes were identified. H-NS binding stimulating DNA bridging has become the accepted mechanism, whereas H-NS binding causing DNA stiffening has been largely ignored. Here, we report that both modes exist, and that changes in divalent cations drive a switch between them. The stiffening form is present under physiological conditions, and directly responds to pH and temperature in vitro. Our findings have broad implications and require a reinterpretation of the mechanism by which H-NS regulates genes.
热稳定核结构蛋白(H-NS)是一种丰富的原核蛋白,在组织染色体 DNA 和基因沉默方面发挥着重要作用。已经确定了两种有争议的结合模式。H-NS 结合刺激 DNA 桥接已成为公认的机制,而 H-NS 结合导致 DNA 变硬是很大程度上被忽视的。在这里,我们报告说这两种模式都存在,并且二价阳离子的变化会导致它们之间的转换。在生理条件下存在变僵硬的形式,并在体外直接响应 pH 值和温度。我们的发现具有广泛的意义,需要重新解释 H-NS 调节基因的机制。