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本文引用的文献

1
Physical association and coordinate function of the H3 K4 methyltransferase MLL1 and the H4 K16 acetyltransferase MOF.H3 K4 甲基转移酶MLL1与H4 K16 乙酰转移酶MOF的物理关联及协同功能
Cell. 2005 Jun 17;121(6):873-85. doi: 10.1016/j.cell.2005.04.031.
2
WDR5 associates with histone H3 methylated at K4 and is essential for H3 K4 methylation and vertebrate development.WD重复结构域5(WDR5)与在赖氨酸4(K4)处发生甲基化的组蛋白H3相关联,并且对于H3 K4甲基化和脊椎动物发育至关重要。
Cell. 2005 Jun 17;121(6):859-72. doi: 10.1016/j.cell.2005.03.036.
3
Global and Hox-specific roles for the MLL1 methyltransferase.MLL1甲基转移酶在全局和Hox特异性方面的作用。
Proc Natl Acad Sci U S A. 2005 Jun 14;102(24):8603-8. doi: 10.1073/pnas.0503072102. Epub 2005 Jun 7.
4
Genomic maps and comparative analysis of histone modifications in human and mouse.人类和小鼠的基因组图谱及组蛋白修饰的比较分析
Cell. 2005 Jan 28;120(2):169-81. doi: 10.1016/j.cell.2005.01.001.
5
Histone demethylation mediated by the nuclear amine oxidase homolog LSD1.由核胺氧化酶同源物LSD1介导的组蛋白去甲基化作用
Cell. 2004 Dec 29;119(7):941-53. doi: 10.1016/j.cell.2004.12.012.
6
MLL: a histone methyltransferase disrupted in leukemia.MLL:一种在白血病中被破坏的组蛋白甲基转移酶。
Trends Mol Med. 2004 Oct;10(10):500-7. doi: 10.1016/j.molmed.2004.08.005.
7
Leukemia proto-oncoprotein MLL forms a SET1-like histone methyltransferase complex with menin to regulate Hox gene expression.白血病原癌蛋白MLL与Menin形成一种类似SET1的组蛋白甲基转移酶复合物,以调节Hox基因的表达。
Mol Cell Biol. 2004 Jul;24(13):5639-49. doi: 10.1128/MCB.24.13.5639-5649.2004.
8
A conserved non-homeodomain Hoxa9 isoform interacting with CBP is co-expressed with the 'typical' Hoxa9 protein during embryogenesis.
Gene Expr Patterns. 2004 Mar;4(2):215-22. doi: 10.1016/j.modgep.2003.08.006.
9
Definitive hematopoiesis requires the mixed-lineage leukemia gene.确定性造血需要混合谱系白血病基因。
Dev Cell. 2004 Mar;6(3):437-43. doi: 10.1016/s1534-5807(04)00061-9.
10
Menin associates with a trithorax family histone methyltransferase complex and with the hoxc8 locus.Menin与一个三胸节家族组蛋白甲基转移酶复合物以及hoxc8基因座相关联。
Mol Cell. 2004 Feb 27;13(4):587-97. doi: 10.1016/s1097-2765(04)00081-4.

MLL 特异性地与转录活跃靶基因的一个子集相关联。

MLL associates specifically with a subset of transcriptionally active target genes.

作者信息

Milne Thomas A, Dou Yali, Martin Mary Ellen, Brock Hugh W, Roeder Robert G, Hess Jay L

机构信息

Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.

出版信息

Proc Natl Acad Sci U S A. 2005 Oct 11;102(41):14765-70. doi: 10.1073/pnas.0503630102. Epub 2005 Sep 30.

DOI:10.1073/pnas.0503630102
PMID:16199523
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1253553/
Abstract

MLL (mixed-lineage leukemia) is a histone H3 Lys-4 specific methyltransferase that is a positive regulator of Hox expression. MLL rearrangements and amplification are common in acute lymphoid and myeloid leukemias and myelodysplastic disorders and are associated with abnormal up-regulation of Hox gene expression. Although MLL is expressed throughout hematopoiesis, Hox gene expression is sharply down-regulated during differentiation, suggesting that either the activity of MLL or its association with target promoters must be regulated. Here we show that MLL associates with actively transcribed genes but does not remain bound after transcriptional down-regulation. Surprisingly, MLL is associated not only with promoter regions but also is distributed across the entire coding regions of genes. MLL interacts with RNA polymerase II (pol II) and colocalizes with RNA pol II at a subset of actively transcribed target in vivo. Loss of function Mll results in defects in RNA pol II distribution. Together the results suggest that an intimate association between MLL and RNA pol II occurs at MLL target genes in vivo that is required for normal initiation and/or transcriptional elongation.

摘要

混合谱系白血病(MLL)是一种组蛋白H3赖氨酸-4特异性甲基转移酶,是Hox表达的正向调节因子。MLL重排和扩增在急性淋巴细胞白血病、急性髓细胞白血病以及骨髓增生异常综合征中很常见,并且与Hox基因表达的异常上调有关。尽管MLL在整个造血过程中均有表达,但Hox基因表达在分化过程中会急剧下调,这表明要么MLL的活性,要么其与靶启动子的结合必须受到调控。在此我们表明,MLL与活跃转录的基因相关联,但在转录下调后不会持续结合。令人惊讶的是,MLL不仅与启动子区域相关联,还分布在基因的整个编码区域。MLL与RNA聚合酶II(pol II)相互作用,并在体内与RNA pol II在一部分活跃转录的靶标处共定位。功能缺失的Mll会导致RNA pol II分布出现缺陷。这些结果共同表明,在体内MLL靶基因处,MLL与RNA pol II之间存在紧密关联,这是正常起始和/或转录延伸所必需的。