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本文引用的文献

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Wheels within wheels: new transcriptional feedback loops in the Arabidopsis circadian clock.层层嵌套:拟南芥生物钟中新的转录反馈环
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CLOCK:BMAL1 is a pioneer-like transcription factor.时钟基因:BMAL1 是一种先驱样转录因子。
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Wheels within wheels: the plant circadian system.重重嵌套:植物生物钟系统。
Trends Plant Sci. 2014 Apr;19(4):240-9. doi: 10.1016/j.tplants.2013.11.007. Epub 2013 Dec 24.
4
Ethylene-insensitive3 is a senescence-associated gene that accelerates age-dependent leaf senescence by directly repressing miR164 transcription in Arabidopsis.乙烯不敏感3是一种衰老相关基因,它通过直接抑制拟南芥中miR164的转录来加速依赖年龄的叶片衰老。
Plant Cell. 2013 Sep;25(9):3311-28. doi: 10.1105/tpc.113.113340. Epub 2013 Sep 24.
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LNK genes integrate light and clock signaling networks at the core of the Arabidopsis oscillator.LNK 基因整合了光信号和时钟信号网络,处于拟南芥生物钟振荡器的核心。
Proc Natl Acad Sci U S A. 2013 Jul 16;110(29):12120-5. doi: 10.1073/pnas.1302170110. Epub 2013 Jul 1.
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Accurate timekeeping is controlled by a cycling activator in Arabidopsis.拟南芥中的一个循环激活因子控制着精确的计时。
Elife. 2013 Apr 30;2:e00473. doi: 10.7554/eLife.00473.
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ELF4 regulates GIGANTEA chromatin access through subnuclear sequestration.ELF4 通过亚核隔离调节 GIGANTEA 染色质的可及性。
Cell Rep. 2013 Mar 28;3(3):671-7. doi: 10.1016/j.celrep.2013.02.021. Epub 2013 Mar 21.
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Chromatin remodeling and alternative splicing: pre- and post-transcriptional regulation of the Arabidopsis circadian clock.染色质重塑和可变剪接:拟南芥生物钟的转录前和转录后调控。
Semin Cell Dev Biol. 2013 May;24(5):399-406. doi: 10.1016/j.semcdb.2013.02.009. Epub 2013 Mar 15.
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The circadian epigenome: how metabolism talks to chromatin remodeling.生物钟的表观基因组:代谢与染色质重塑的对话。
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10
Transcriptional corepressor TOPLESS complexes with pseudoresponse regulator proteins and histone deacetylases to regulate circadian transcription.转录核心抑制因子 TOPLESS 复合物与伪应答调节蛋白和组蛋白去乙酰化酶一起调节生物钟转录。
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LNK1和LNK2是拟南芥生物钟振荡器中的转录共激活因子。

LNK1 and LNK2 are transcriptional coactivators in the Arabidopsis circadian oscillator.

作者信息

Xie Qiguang, Wang Peng, Liu Xian, Yuan Li, Wang Lingbao, Zhang Chenguang, Li Yue, Xing Hongya, Zhi Liya, Yue Zhiliang, Zhao Chunsheng, McClung C Robertson, Xu Xiaodong

机构信息

Hebei Key Laboratory of Molecular and Cellular Biology, Key Laboratory of Molecular and Cellular Biology of the Ministry of Education, College of Life Sciences, Hebei Normal University, Hebei Collaboration Innovation Center for Cell Signaling, Shijiazhuang, Hebei 050024, China.

Department of Biological Sciences, Dartmouth College, Hanover, New Hampshire 03755-3563.

出版信息

Plant Cell. 2014 Jul;26(7):2843-57. doi: 10.1105/tpc.114.126573. Epub 2014 Jul 10.

DOI:10.1105/tpc.114.126573
PMID:25012192
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4145118/
Abstract

Transcriptional feedback loops are central to the architecture of eukaryotic circadian clocks. Models of the Arabidopsis thaliana circadian clock have emphasized transcriptional repressors, but recently, Myb-like REVEILLE (RVE) transcription factors have been established as transcriptional activators of central clock components, including PSEUDO-RESPONSE REGULATOR5 (PRR5) and TIMING OF CAB EXPRESSION1 (TOC1). We show here that NIGHT LIGHT-INDUCIBLE AND CLOCK-REGULATED1 (LNK1) and LNK2, members of a small family of four LNK proteins, dynamically interact with morning-expressed oscillator components, including RVE4 and RVE8. Mutational disruption of LNK1 and LNK2 function prevents transcriptional activation of PRR5 by RVE8. The LNKs lack known DNA binding domains, yet LNK1 acts as a transcriptional activator in yeast and in planta. Chromatin immunoprecipitation shows that LNK1 is recruited to the PRR5 and TOC1 promoters in planta. We conclude that LNK1 is a transcriptional coactivator necessary for expression of the clock genes PRR5 and TOC1 through recruitment to their promoters via interaction with bona fide DNA binding proteins such as RVE4 and RVE8.

摘要

转录反馈环是真核生物钟结构的核心。拟南芥生物钟模型一直强调转录抑制因子,但最近,类Myb的唤醒(REVEILLE,RVE)转录因子已被确立为核心生物钟组分的转录激活因子,包括伪应答调节因子5(PSEUDO-RESPONSE REGULATOR5,PRR5)和CAB表达时间1(TIMING OF CAB EXPRESSION1,TOC1)。我们在此表明,夜灯诱导和生物钟调节1(NIGHT LIGHT-INDUCIBLE AND CLOCK-REGULATED1,LNK1)和LNK2是由4个LNK蛋白组成的小家族成员,它们与早晨表达的振荡器组分动态相互作用,包括RVE4和RVE8。LNK1和LNK2功能的突变破坏会阻止RVE8对PRR5的转录激活。LNKs缺乏已知的DNA结合结构域,但LNK1在酵母和植物中均作为转录激活因子发挥作用。染色质免疫沉淀表明,LNK1在植物中被招募到PRR5和TOC1启动子区域。我们得出结论,LNK1是一种转录共激活因子,通过与诸如RVE4和RVE8等真正的DNA结合蛋白相互作用,被招募到PRR5和TOC1启动子区域,从而对生物钟基因PRR5和TOC1的表达是必需的。