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果蝇中的生物钟机制。

Clock mechanisms in Drosophila.

作者信息

Stanewsky Ralf

机构信息

Universität Regensburg, Institut für Zoologie, Lehrstuhl für Entwicklungsbiologie, Universitätsstrasse 31, 93040 Regensburg, Germany.

出版信息

Cell Tissue Res. 2002 Jul;309(1):11-26. doi: 10.1007/s00441-002-0569-0. Epub 2002 May 29.

Abstract

Mechanisms underlying circadian clock function in Drosophila melanogaster have been revealed by genetic and molecular approaches. Two interlocked transcriptional feedback loops involving at least the period, timeless, Clock,and cycle genes generate molecular oscillations that are believed to control behavioral rhythmicity and other clock outputs. These oscillations are further enhanced and fine-tuned to match the duration of the solar day by post-transcriptional and post-translational mechanisms depending on the PERIOD and TIMELESS proteins and on the protein kinases DOUBLE-TIME and SHAGGY. Light is the principal zeitgeber for synchronizing molecular and behavioral rhythmicity via the blue-light photoreceptor CRYPTOCHROME and the TIMELESS protein. In addition, light seems required for maintaining robust molecular oscillations at least in peripheral clock-gene-expressing tissues like the eyes, antennae, or Malpighian tubules. Relaying temporal information to cells and tissues expressing overt biological rhythms involves regulation of "output genes" at multiple levels. Although their regulation depends on the major clock genes, the majority of the clock-controlled genes are not direct targets of clock factors.

摘要

通过遗传和分子方法,黑腹果蝇昼夜节律钟功能的潜在机制已被揭示。两个相互关联的转录反馈环,至少涉及周期基因(period)、无时间基因(timeless)、生物钟基因(Clock)和周期蛋白基因(cycle),产生分子振荡,据信这种振荡控制着行为节律性和其他生物钟输出。这些振荡通过依赖于周期蛋白(PERIOD)和无时间蛋白(TIMELESS)以及蛋白激酶双倍时间蛋白(DOUBLE-TIME)和蓬乱蛋白(SHAGGY)的转录后和翻译后机制,进一步增强并微调以匹配太阳日的时长。光是通过蓝光光感受器隐花色素(CRYPTOCHROME)和无时间蛋白(TIMELESS)来同步分子和行为节律性的主要授时因子。此外,至少在眼睛、触角或马氏管等表达外周生物钟基因的组织中,维持强大的分子振荡似乎需要光。将时间信息传递到表达明显生物节律的细胞和组织涉及在多个层面上对“输出基因”的调控。尽管它们的调控依赖于主要的生物钟基因,但大多数生物钟控制基因并非生物钟因子的直接靶标。

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