Global and Hox-specific roles for the MLL1 methyltransferase

Proc Natl Acad Sci U S A. 2005 Jun 14;102(24):8603-8. doi: 10.1073/pnas.0503072102. Epub 2005 Jun 7.

Abstract

The mixed-lineage leukemia (MLL1/ALL-1/HRX) histone methyltransferase is involved in the epigenetic maintenance of transcriptional memory and the pathogenesis of human leukemias. To understand its role in cell type specification, we determined the human genomic binding sites of MLL1. We found that MLL1 functions as a human equivalent of yeast Set1. Like Set1, MLL1 localizes with RNA polymerase II (Pol II) to the 5' end of actively transcribed genes, where histone H3 lysine 4 trimethylation occurs. Consistent with this global role in transcription, MLL1 also localizes to microRNA (miRNA) loci that are involved in leukemia and hematopoiesis. In contrast to the 5' proximal binding behavior at most protein-coding genes, MLL1 occupies an extensive domain within a transcriptionally active region of the HoxA cluster. The ability of MLL1 to serve as a start site-specific global transcriptional regulator and to participate in larger chromatin domains at the Hox genes reveals dual roles for MLL1 in maintenance of cellular identity.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Chromatin Immunoprecipitation
  • Chromosomes, Human, Pair 7 / genetics
  • Chromosomes, Human, Pair 7 / metabolism*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Gene Expression Regulation / genetics*
  • Genes, Homeobox / genetics
  • Genes, Regulator / genetics*
  • Genome, Human*
  • Genomics / methods
  • Histone Methyltransferases
  • Histone-Lysine N-Methyltransferase / metabolism*
  • Humans
  • MicroRNAs / metabolism
  • Myeloid-Lymphoid Leukemia Protein
  • Oligonucleotide Array Sequence Analysis
  • Protein Methyltransferases
  • Proto-Oncogenes / genetics
  • RNA Polymerase II / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • DNA-Binding Proteins
  • KMT2A protein, human
  • MicroRNAs
  • Transcription Factors
  • Myeloid-Lymphoid Leukemia Protein
  • Histone Methyltransferases
  • Protein Methyltransferases
  • Histone-Lysine N-Methyltransferase
  • RNA Polymerase II