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核应激颗粒:睡美人苏醒了?

Nuclear stress granules: the awakening of a sleeping beauty?

作者信息

Sandqvist Anton, Sistonen Lea

机构信息

Turku Centre for Biotechnology, BioCity, P.O. Box 123, FIN-20521 Turku, Finland.

出版信息

J Cell Biol. 2004 Jan 5;164(1):15-7. doi: 10.1083/jcb.200311102.

DOI:10.1083/jcb.200311102
PMID:14709538
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2171964/
Abstract

Nuclear stress granules are subnuclear compartments that form in response to heat shock and other stress stimuli. Although many components of nuclear stress granules have been identified, including HSF1 and pre-mRNA processing factors, their function remains a mystery. A paper in this issue describes the stress-induced transcriptional activation of one of the nuclear stress granule target sites, a heterochromatic region that has been considered silent (Jolly et al., 2004). These intriguing findings will certainly give the research of these structures a new twist.

摘要

核应激颗粒是在热休克和其他应激刺激下形成的亚核区室。尽管已经鉴定出核应激颗粒的许多成分,包括热休克因子1(HSF1)和前体mRNA加工因子,但其功能仍然是个谜。本期的一篇论文描述了核应激颗粒靶位点之一(一个被认为是沉默的异染色质区域)的应激诱导转录激活(乔利等人,2004年)。这些有趣的发现必将为这些结构的研究带来新的转折。

相似文献

1
Nuclear stress granules: the awakening of a sleeping beauty?核应激颗粒:睡美人苏醒了?
J Cell Biol. 2004 Jan 5;164(1):15-7. doi: 10.1083/jcb.200311102.
2
Stress-induced transcription of satellite III repeats.应激诱导的卫星III重复序列转录。
J Cell Biol. 2004 Jan 5;164(1):25-33. doi: 10.1083/jcb.200306104. Epub 2003 Dec 29.
3
In vivo binding of active heat shock transcription factor 1 to human chromosome 9 heterochromatin during stress.应激期间活性热休克转录因子1在体内与人类9号染色体异染色质的结合。
J Cell Biol. 2002 Mar 4;156(5):775-81. doi: 10.1083/jcb.200109018.
4
A key role for stress-induced satellite III transcripts in the relocalization of splicing factors into nuclear stress granules.应激诱导的卫星III转录本在剪接因子重新定位到核应激颗粒中的关键作用。
J Cell Sci. 2004 Sep 1;117(Pt 19):4551-8. doi: 10.1242/jcs.01329.
5
Transcriptional activation of a constitutive heterochromatic domain of the human genome in response to heat shock.人类基因组组成型异染色质结构域对热休克的转录激活。
Mol Biol Cell. 2004 Feb;15(2):543-51. doi: 10.1091/mbc.e03-07-0487. Epub 2003 Nov 14.
6
Structural and functional characterization of noncoding repetitive RNAs transcribed in stressed human cells.应激人类细胞中转录的非编码重复RNA的结构与功能特征
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Chromosome Y pericentric heterochromatin is a primary target of HSF1 in male cells.Y 染色体着丝粒异染色质是雄性细胞中 HSF1 的主要靶标。
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Heat shock factor 1 binds to and transcribes satellite II and III sequences at several pericentromeric regions in heat-shocked cells.热休克因子 1 在热休克细胞中结合并转录几个着丝粒周围区域的卫星 II 和 III 序列。
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Multiple pathways for telomere tethering: functional implications of subnuclear position for heterochromatin formation.端粒锚定的多种途径:亚核位置对异染色质形成的功能影响
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引用本文的文献

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Acta Biochim Biophys Sin (Shanghai). 2023 Jul 3;55(7):1099-1118. doi: 10.3724/abbs.2023117.
2
Tellurite Promotes Stress Granules and Nuclear SG-Like Assembly in Response to Oxidative Stress and DNA Damage.亚碲酸盐在应对氧化应激和DNA损伤时促进应激颗粒和核内类应激颗粒的组装。
Front Cell Dev Biol. 2021 Feb 11;9:622057. doi: 10.3389/fcell.2021.622057. eCollection 2021.
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Hum Genet. 2017 Sep;136(9):1173-1191. doi: 10.1007/s00439-017-1835-2. Epub 2017 Aug 29.
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Acute exercise boosts cell proliferation and the heat shock response in lymphocytes: correlation with cytokine production and extracellular-to-intracellular HSP70 ratio.急性运动可促进淋巴细胞的细胞增殖和热休克反应:与细胞因子产生及细胞外与细胞内HSP70比值的相关性
Cell Stress Chaperones. 2017 Mar;22(2):271-291. doi: 10.1007/s12192-017-0771-3. Epub 2017 Mar 1.
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Relationships between Stress Granules, Oxidative Stress, and Neurodegenerative Diseases.应激颗粒、氧化应激与神经退行性疾病之间的关系
Oxid Med Cell Longev. 2017;2017:1809592. doi: 10.1155/2017/1809592. Epub 2017 Jan 18.
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Neuronal serotonin release triggers the heat shock response in C. elegans in the absence of temperature increase.在不升高温度的情况下,神经元血清素释放会触发秀丽隐杆线虫的热休克反应。
Curr Biol. 2015 Jan 19;25(2):163-174. doi: 10.1016/j.cub.2014.11.040. Epub 2014 Dec 31.
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Inducible hsp70 in the regulation of cancer cell survival: analysis of chaperone induction, expression and activity.诱导型热休克蛋白 70 在癌细胞存活调控中的作用:伴侣蛋白诱导、表达与活性分析。
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Impaired heat shock response in cells expressing full-length polyglutamine-expanded huntingtin.表达全长多聚谷氨酰胺扩展 huntingtin 的细胞中热休克反应受损。
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本文引用的文献

1
Stress-induced transcription of satellite III repeats.应激诱导的卫星III重复序列转录。
J Cell Biol. 2004 Jan 5;164(1):25-33. doi: 10.1083/jcb.200306104. Epub 2003 Dec 29.
2
Transcriptional activation of a constitutive heterochromatic domain of the human genome in response to heat shock.人类基因组组成型异染色质结构域对热休克的转录激活。
Mol Biol Cell. 2004 Feb;15(2):543-51. doi: 10.1091/mbc.e03-07-0487. Epub 2003 Nov 14.
3
Formation of nuclear stress granules involves HSF2 and coincides with the nucleolar localization of Hsp70.核应激颗粒的形成涉及热休克因子2(HSF2),且与热休克蛋白70(Hsp70)的核仁定位同时发生。
J Cell Sci. 2003 Sep 1;116(Pt 17):3557-70. doi: 10.1242/jcs.00671. Epub 2003 Jul 15.
4
Coordinated methyl and RNA binding is required for heterochromatin localization of mammalian HP1alpha.哺乳动物HP1α的异染色质定位需要甲基和RNA的协同结合。
EMBO Rep. 2002 Oct;3(10):975-81. doi: 10.1093/embo-reports/kvf194. Epub 2002 Sep 13.
5
Regulation of heterochromatic silencing and histone H3 lysine-9 methylation by RNAi.RNA干扰对异染色质沉默和组蛋白H3赖氨酸-9甲基化的调控。
Science. 2002 Sep 13;297(5588):1833-7. doi: 10.1126/science.1074973. Epub 2002 Aug 22.
6
Human chromosomes 9, 12, and 15 contain the nucleation sites of stress-induced nuclear bodies.人类9号、12号和15号染色体包含应激诱导核仁的成核位点。
Mol Biol Cell. 2002 Jun;13(6):2069-79. doi: 10.1091/mbc.01-12-0569.
7
X-chromosome inactivation and the search for chromosome-wide silencers.X染色体失活与全染色体范围沉默子的寻找
Curr Opin Genet Dev. 2002 Apr;12(2):219-24. doi: 10.1016/s0959-437x(02)00289-7.
8
In vivo binding of active heat shock transcription factor 1 to human chromosome 9 heterochromatin during stress.应激期间活性热休克转录因子1在体内与人类9号染色体异染色质的结合。
J Cell Biol. 2002 Mar 4;156(5):775-81. doi: 10.1083/jcb.200109018.
9
Higher-order structure in pericentric heterochromatin involves a distinct pattern of histone modification and an RNA component.着丝粒周围异染色质中的高阶结构涉及独特的组蛋白修饰模式和一个RNA成分。
Nat Genet. 2002 Mar;30(3):329-34. doi: 10.1038/ng843. Epub 2002 Feb 19.
10
Stress-induced nuclear bodies are sites of accumulation of pre-mRNA processing factors.应激诱导的核小体是前体mRNA加工因子积累的位点。
Mol Biol Cell. 2001 Nov;12(11):3502-14. doi: 10.1091/mbc.12.11.3502.