Mechanisms of transformation by MLL

Research output: Contribution to journalArticle

68 Citations (Scopus)

Abstract

Rearrangements of the mixed-lineage leukemia gene MLL1 (MLL, HRX, ALL1), the human homologue of the Drosophila gene trithorax, are associated with aggressive acute leukemias in both children and adults. Transformation by rearranged forms of MLL1, including in-frame fusion proteins, partial tandem duplications, and amplification of MLL1 through upregulation of Hox gene and cofactor expression apparently results in a block in hematopoietic differentiation. MLL1 regulates Hox gene expression via direct promoter binding and histone H3 Lys 4 methylation mediated by the intrinsic methyltransferase activity of the SET domain. Mll1 knockout leads to loss of Hox gene expression, defects in hematopoiesis, and embryonic lethality. A close homologue, MLL2 is amplified in some solid tumors. MLL2 also has histone H3 Lys 4 methyltransferase activity that is dependent on menin, a protein mutated in multiple neoplasia type I (MEN1) and which is required for normal Hox expression. These findings underscore the importance of the MLL histone methyltransferases in development and disease.

Original languageEnglish (US)
Pages (from-to)235-254
Number of pages20
JournalCritical Reviews in Eukaryotic Gene Expression
Volume14
Issue number4
DOIs
StatePublished - 2004
Externally publishedYes

Fingerprint

Homeobox Genes
Methyltransferases
Gene Expression
Histones
Leukemia
Multiple Endocrine Neoplasia Type 1
Hematopoiesis
Methylation
Genes
Drosophila
Neoplasms
Proteins
Up-Regulation

Keywords

  • Histone methylation
  • Hox genes
  • Mixed-lineage leukemia
  • Multiple endocrine neoplasia

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics

Cite this

Mechanisms of transformation by MLL. / Hess, Jay.

In: Critical Reviews in Eukaryotic Gene Expression, Vol. 14, No. 4, 2004, p. 235-254.

Research output: Contribution to journalArticle

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