Reflections on contributing to “big discoveries” about the fly clock: Our fortunate paths as post-docs with 2017 Nobel laureates Jeff Hall, Michael Rosbash, and Mike Young

Q2 Medicine
Kathleen K. Siwicki , Paul E. Hardin , Jeffrey L. Price
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引用次数: 4

Abstract

In the early 1980s Jeff Hall and Michael Rosbash at Brandeis University and Mike Young at Rockefeller University set out to isolate the period (per) gene, which was recovered in a revolutionary genetic screen by Ron Konopka and Seymour Benzer for mutants that altered circadian behavioral rhythms. Over the next 15 years the Hall, Rosbash and Young labs made a series of groundbreaking discoveries that defined the molecular timekeeping mechanism and formed the basis for them being awarded the 2017 Nobel Prize in Physiology or Medicine. Here the authors recount their experiences as post-docs in the Hall, Rosbash and Young labs from the mid-1980s to the mid-1990s, and provide a perspective of how basic research conducted on a simple model system during that era profoundly influenced the direction of the clocks field and established novel approaches that are now standard operating procedure for studying complex behavior.

Abstract Image

Abstract Image

为果蝇时钟的“重大发现”做出贡献的思考:我们与2017年诺贝尔奖得主杰夫·霍尔、迈克尔·罗斯巴什和迈克·杨一起成为博士后的幸运之路
20世纪80年代初,布兰代斯大学的杰夫·霍尔和迈克尔·罗斯巴什以及洛克菲勒大学的迈克·杨开始分离周期基因,这种基因是由罗恩·科诺普卡和西摩·本泽在一种革命性的基因筛选中发现的,用于改变昼夜行为节奏的突变体。在接下来的15年里,霍尔、罗斯巴什和杨的实验室取得了一系列突破性的发现,这些发现定义了分子计时机制,并为他们获得2017年诺贝尔生理学或医学奖奠定了基础。在这里,作者讲述了他们从20世纪80年代中期到90年代中期在霍尔、罗斯巴什和杨实验室做博士后的经历,并提供了一个视角,说明在那个时代,对一个简单模型系统进行的基础研究如何深刻地影响了时钟领域的方向,并建立了新的方法,这些方法现在是研究复杂行为的标准操作程序。
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来源期刊
Neurobiology of Sleep and Circadian Rhythms
Neurobiology of Sleep and Circadian Rhythms Neuroscience-Behavioral Neuroscience
CiteScore
4.50
自引率
0.00%
发文量
9
审稿时长
69 days
期刊介绍: Neurobiology of Sleep and Circadian Rhythms is a multidisciplinary journal for the publication of original research and review articles on basic and translational research into sleep and circadian rhythms. The journal focuses on topics covering the mechanisms of sleep/wake and circadian regulation from molecular to systems level, and on the functional consequences of sleep and circadian disruption. A key aim of the journal is the translation of basic research findings to understand and treat sleep and circadian disorders. Topics include, but are not limited to: Basic and translational research, Molecular mechanisms, Genetics and epigenetics, Inflammation and immunology, Memory and learning, Neurological and neurodegenerative diseases, Neuropsychopharmacology and neuroendocrinology, Behavioral sleep and circadian disorders, Shiftwork, Social jetlag.
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