The amino terminus of the mixed lineage leukemia protein (MLL) promotes cell cycle arrest and monocytic differentiation

Corrado Caslini, Ali Shilatifard, Liping Yang, Jay Hess

Research output: Contribution to journalArticle

51 Citations (Scopus)

Abstract

Several lines of evidence suggest that the mixed lineage leukemia protein (MLL, ALL-1, HRX) plays a role in regulating myelomonocytic differentiation, in this study we examined the effect of expression of MLL- AF9 on differentiation of the monoblastic U937 cell line by using a tetracycline-inducible expression system. MLL-AF9 arrested growth of U937 cells and induced these cells to differentiate into macrophages; induction was accompanied by expression of CD11b and CD14 and ultimately cell death. Deletion mutants of MLL-AF9 were used to map the sequences responsible for this effect. The amino-terminal half of MLL was sufficient for both cell cycle arrest and macrophage differentiation, whereas the carboxyl terminus of MLL or AF9 was found to be dispensable for this effect. Further deletions showed that a 35-kDa amino-terminal fragment spanning two AT hook motifs was sufficient for cell cycle arrest, up-regulation of p21(Cip1) and p27(Kip1), and partial differentiation toward macrophages. These findings suggest a possible role for the MLL AT hook-containing region in regulating myelomonocytic differentiation.

Original languageEnglish (US)
Pages (from-to)2797-2802
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume97
Issue number6
DOIs
StatePublished - Mar 14 2000
Externally publishedYes

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Myeloid-Lymphoid Leukemia Protein
Cell Cycle Checkpoints
AT-Hook Motifs
U937 Cells
Macrophages
Tetracycline
Cell Death
Up-Regulation

ASJC Scopus subject areas

  • Genetics
  • General

Cite this

The amino terminus of the mixed lineage leukemia protein (MLL) promotes cell cycle arrest and monocytic differentiation. / Caslini, Corrado; Shilatifard, Ali; Yang, Liping; Hess, Jay.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 97, No. 6, 14.03.2000, p. 2797-2802.

Research output: Contribution to journalArticle

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