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本文引用的文献

1
JmjC-domain-containing proteins and histone demethylation.含JmjC结构域的蛋白质与组蛋白去甲基化
Nat Rev Genet. 2006 Sep;7(9):715-27. doi: 10.1038/nrg1945.
2
Regulation of MLL1 H3K4 methyltransferase activity by its core components.其核心组分对MLL1 H3K4甲基转移酶活性的调控
Nat Struct Mol Biol. 2006 Aug;13(8):713-9. doi: 10.1038/nsmb1128. Epub 2006 Jul 30.
3
Genomic binding and transcriptional regulation by the Drosophila Myc and Mnt transcription factors.果蝇Myc和Mnt转录因子的基因组结合与转录调控
Cold Spring Harb Symp Quant Biol. 2005;70:299-307. doi: 10.1101/sqb.2005.70.019.
4
From genetics to epigenetics: the tale of Polycomb group and trithorax group genes.从遗传学到表观遗传学:多梳蛋白家族和三胸节蛋白家族基因的故事
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Myc-binding-site recognition in the human genome is determined by chromatin context.人类基因组中Myc结合位点的识别由染色质环境决定。
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6
Jmjd2b antagonizes H3K9 trimethylation at pericentric heterochromatin in mammalian cells.Jmjd2b在哺乳动物细胞中拮抗着丝粒周围异染色质上的H3K9三甲基化。
Genes Dev. 2006 Jun 15;20(12):1557-62. doi: 10.1101/gad.388206. Epub 2006 May 31.
7
The putative oncogene GASC1 demethylates tri- and dimethylated lysine 9 on histone H3.假定的癌基因GASC1可使组蛋白H3上的赖氨酸9发生三甲基化和二甲基化去甲基化。
Nature. 2006 Jul 20;442(7100):307-11. doi: 10.1038/nature04837. Epub 2006 May 28.
8
The transcriptional repressor JHDM3A demethylates trimethyl histone H3 lysine 9 and lysine 36.转录抑制因子JHDM3A可使三甲基化组蛋白H3赖氨酸9和赖氨酸36发生去甲基化。
Nature. 2006 Jul 20;442(7100):312-6. doi: 10.1038/nature04853. Epub 2006 May 28.
9
A PHD finger of NURF couples histone H3 lysine 4 trimethylation with chromatin remodelling.NURF的一个PHD指结构域将组蛋白H3赖氨酸4三甲基化与染色质重塑联系起来。
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10
Myc influences global chromatin structure.Myc影响整体染色质结构。
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三体胸蛋白Lid是dMyc诱导细胞生长所需的一种组蛋白H3K4三甲基去甲基化酶。

The Trithorax group protein Lid is a trimethyl histone H3K4 demethylase required for dMyc-induced cell growth.

作者信息

Secombe Julie, Li Ling, Carlos Leni, Eisenman Robert N

机构信息

Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.

出版信息

Genes Dev. 2007 Mar 1;21(5):537-51. doi: 10.1101/gad.1523007. Epub 2007 Feb 20.

DOI:10.1101/gad.1523007
PMID:17311883
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1820896/
Abstract

The Myc oncoprotein is a potent inducer of cell growth, cell cycle progression, and apoptosis. While many direct Myc target genes have been identified, the molecular determinants of Myc's transcriptional specificity remain elusive. We have carried out a genetic screen in Drosophila and identified the Trithorax group protein Little imaginal discs (Lid) as a regulator of dMyc-induced cell growth. Lid binds to dMyc and is required for dMyc-induced expression of the growth regulatory gene Nop60B. The mammalian Lid orthologs, Rbp-2 (JARID1A) and Plu-1 (JARID1B), also bind to c-Myc, indicating that Lid-Myc function is conserved. We demonstrate that Lid is a JmjC-dependent trimethyl H3K4 demethylase in vivo and that this enzymatic activity is negatively regulated by dMyc, which binds to Lid's JmjC domain. Because Myc binding is associated with high levels of trimethylated H3K4, we propose that the Lid-dMyc complex facilitates Myc binding to, or maintenance of, this chromatin context.

摘要

Myc癌蛋白是细胞生长、细胞周期进程和细胞凋亡的强效诱导剂。虽然已经鉴定出许多直接的Myc靶基因,但Myc转录特异性的分子决定因素仍然难以捉摸。我们在果蝇中进行了一项遗传筛选,并鉴定出三胸复合物蛋白小成虫盘(Lid)是dMyc诱导的细胞生长的调节因子。Lid与dMyc结合,并且是dMyc诱导生长调节基因Nop60B表达所必需的。哺乳动物的Lid直系同源物Rbp-2(JARID1A)和Plu-1(JARID1B)也与c-Myc结合,表明Lid-Myc功能是保守的。我们证明Lid在体内是一种依赖JmjC的三甲基化H3K4去甲基化酶,并且这种酶活性受到dMyc的负调控,dMyc与Lid的JmjC结构域结合。由于Myc结合与高水平的三甲基化H3K4相关,我们提出Lid-dMyc复合物促进Myc与这种染色质环境的结合或维持。