Sun Liming, Wang Huayi, Hu Ji, Han Jinlong, Matsunami Hiroaki, Luo Minmin
National Institute of Biological Sciences, Beijing 102206 China.
Proc Natl Acad Sci U S A. 2009 Feb 10;106(6):2041-6. doi: 10.1073/pnas.0812220106. Epub 2009 Jan 30.
Atmospheric CO(2) is an important environmental cue that regulates several types of animal behavior. In mice, CO(2) responses of the olfactory sensory neurons (OSNs) require the activity of carbonic anhydrase to catalyze the conversion of CO(2) to bicarbonate and the opening of cGMP-sensitive ion channels. However, it remains unknown how the enhancement of bicarbonate levels results in cGMP production. Here, we show that bicarbonate activates cGMP-producing ability of guanylyl cyclase-D (GC-D), a membrane GC exclusively expressed in the CO(2)-responsive OSNs, by directly acting on the intracellular cyclase domain of GC-D. Also, the molecular mechanism for GC-D activation is distinct from the commonly believed model of "release from repression" for other membrane GCs. Our results contribute to our understanding of the molecular mechanisms of CO(2) sensing and suggest diverse mechanisms of molecular activation among membrane GCs.
大气中的二氧化碳是一种重要的环境信号,可调节多种动物行为。在小鼠中,嗅觉感觉神经元(OSN)对二氧化碳的反应需要碳酸酐酶的活性来催化二氧化碳转化为碳酸氢盐,并打开对环鸟苷酸(cGMP)敏感的离子通道。然而,目前尚不清楚碳酸氢盐水平的升高如何导致cGMP的产生。在这里,我们表明,碳酸氢盐通过直接作用于鸟苷酸环化酶-D(GC-D)的细胞内环化酶结构域,激活了GC-D的cGMP生成能力,GC-D是一种仅在对二氧化碳有反应的OSN中表达的膜鸟苷酸环化酶。此外,GC-D激活的分子机制不同于其他膜鸟苷酸环化酶普遍认为的“解除抑制”模型。我们的研究结果有助于我们理解二氧化碳感知的分子机制,并揭示膜鸟苷酸环化酶之间不同的分子激活机制。