MLL associates specifically with a subset of transcriptionally active target genes

被引:174
作者
Milne, TA
Dou, YL
Martin, ME
Brock, HW
Roeder, RG
Hess, JL
机构
[1] Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Med, Philadelphia, PA 19104 USA
[3] Rockefeller Univ, Lab Biochem & Mol Biol, New York, NY 10021 USA
[4] Univ British Columbia, Dept Zool, Vancouver, BC V6T 1Z4, Canada
关键词
histone methyltransferase; Hox genes; transcription;
D O I
10.1073/pnas.0503630102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MILL (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 11 (pol 11) and colocalizes with RNA pol 11 at a subset of actively transcribed target in vivo. Loss of function MY results in defects in RNA pol 11 distribution. Together the results suggest that an intimate association between MLL and RNA pol 11 occurs at MLL target genes in vivo that is required for normal initiation and/or transcriptional elongation.
引用
收藏
页码:14765 / 14770
页数:6
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