Endogeneous DNA double strand breaks in the human and murine MLL gene
J Zech, S Scharf, D Schraets, T Dingermann, R Marschalek · Klinische Pädiatrie · 2004 · Heft 05
Bibliografische Angaben
Zusammenfassung
The human MLL gene is recurrently involved in chromosomal translocations with a large variety of different translocation partner genes. Recent studies have identified two recombination clusters where chromosomal translocations map in the breakpoint cluster region of the human MLL gene. Interestingly, one of these hot spot coincides with chromosomal breakpoints that can be exogenously induced by the application of several substances, including epipodophyllotoxins (VP16 or VM26) or by simply inducing apoptosis. Here we present data about where these DNA double strand breaks occur in the human MLL gene when treated…