Milne Thomas A, Dou Yali, Martin Mary Ellen, Brock Hugh W, Roeder Robert G, Hess Jay L
Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.
Proc Natl Acad Sci U S A. 2005 Oct 11;102(41):14765-70. doi: 10.1073/pnas.0503630102. Epub 2005 Sep 30.
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.
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。