通过昼夜节律分子钟研究来克服神经退行性疾病:-我在国家研究所的30年历史- @@@ -

Q4 Social Sciences
N. Ishida
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引用次数: 0

摘要

哺乳动物生物钟基因Period2是我的研究组在1998年研究生物钟基因时发现的。总结了这一发现后对生物钟分子机制的认识进展。我们的研究小组已经证明了糖原合成酶激酶3依赖性Period2磷酸化及其核转移和E4BP4 (vrille)负转录调控以及Clock/Bmal, Period/Cry E-box依赖性负反馈回路的重要性。肌醇在延长生物钟方面的作用是通过与滋贺县的Tsujiko Co., Ltd在冰厂项目上的合作发现的。当我们开始对生物钟进行分子研究时,我们只考虑日常节律。幸运的是,我们对外围时钟机制(PPARα)的研究揭示了一种新的季节时钟机制,它可以计算光周期以适应冬季(冬眠)。我们这一代研究人员进入日本国立研究所时,经历了一个被称为“基础研究转型时代”的时期。但是,在我们加入研究所后的24到25年间,基础研究经费被大幅削减,我们的研究任务突然变成了应用科学。经过几年的挫折和思考,我们放弃了用老鼠进行研究,转而专注于用果蝇来降低成本和节省时间。因此,我们通过果蝇模型发现了年轻时睡眠异常在两种神经退行性疾病(戈谢氏病和帕金森病)中的致病作用。综述了神经退行性疾病分子机制的应用。从1986年我在工业科学技术局发酵研究所开始担任研究员到现在在AIST,我非常感谢我能够与参与其中的人们一起花了30多年的时间研究分子生物钟。睡眠,神经退行性疾病,戈谢氏病,帕金森病
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Toward overcoming neurodegenerative disease by the circadian molecular clock study: — My 30 year history in a national institute —@@@— 国立研究所30年の総括 —
The mammalian clock gene, Period2 , was discovered by my research group studying clock genes in 1998. I summarize the progress of understanding the circadian clock molecular mechanism after this discovery. Our group has demonstrated the importance of glycogen synthase kinase 3 – dependent phosphorylation of Period2 and its nuclear transfer and E4BP4 (vrille) negative transcriptional regulation, as well as Clock/Bmal, Period/Cry E-box dependent negative feedback loop. A role of myo-inositol for elongation of the circadian clock was uncovered through collaboration on iceplant projects with Tsujiko Co., Ltd, Shiga prefecture. When we started the molecular study of the circadian clock, we only considered the daily rhythm. Fortuitously, our research on the peripheral clock mechanism (PPARα) revealed a new mechanism of seasonal clocks, which can count photoperiods to adapt to winter (torpor). Our generation of researchers entered Japanese national institutes during a period called “the basic research shift era.” But, basic research grants were cut significantly during the 24 to 25 year period after we joined the institutes, and our research mission was abruptly changed to applied science. After several years of frustration and contemplation, we gave up studies using mice and concentrated on using Drosophila to reduce costs and save time. Consequently, we found a causative role of sleep abnormality around a young age in two neurodegenerative (Gaucher’s and Parkinson’s) diseases by using fly models. I summarize an application for the molecular mechanism of neurodegenerative disease. I am greatly thankful that I was able to spend more than 30 years on the study of molecular circadian clocks with the people who have been involved, from when I started as a researcher in 1986 at the Fermentation Research Institute of the Agency of Industrial Science and Technology to the present day at AIST. sleep, Neurodegenerative disease, Gaucher’s disease, Parkinson’s disease
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Synthesiology
Synthesiology Social Sciences-Social Sciences (all)
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