Engineering de novo reciprocal chromosomal translocations associated with Mll to replicate primary events of human cancer

Alan Forster, Richard Pannell, Lesley F. Drynan, Matthew McCormack, Emma C. Collins, Angelika Daser, Terence H. Rabbitts

Research output: Contribution to journalArticleResearchpeer-review

123 Citations (Scopus)


The etiology of human tumors often involves chromosomal translocations. Models that emulate translocations are essential to understanding the determinants of frank malignancy, those dictating the restriction of translocations to specific lineages, and as a basis for development of rational therapeutic methods. We demonstrate that developmentally regulated Cre-loxP-mediated interchromosomal recombination between the Mll gene, whose human counterpart is involved in a spectrum of leukemias, and the Enl gene creates reciprocal chromosomal translocations that cause myeloid tumors. There is a rapid onset and high penetrance of leukemogenesis in these translocator mice, and high proportions of cells carrying chromosomal translocations can be found in bone marrow as early as 12 days after birth. This de novo strategy is a direct recapitulation of naturally occurring human cancer-associated translocations.

Original languageEnglish
Pages (from-to)449-458
Number of pages10
JournalCancer Cell
Issue number5
Publication statusPublished - 1 May 2003
Externally publishedYes

Cite this