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Investigating the long-term and genome-wide effects of the AF4-MLL fusion protein

D Löscher, E Kowarz, R Marschalek · Klinische Pädiatrie · 2015 · Heft 07

Dokument
1200302
CareLit-ID
Jahr
2015
Publikation
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Metadaten
DOI
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Bibliografische Angaben

Zeitschrift
Klinische Pädiatrie
Autor:innen
D Löscher, E Kowarz, R Marschalek
Ausgabe
Heft 07 / 2015
Seiten
–
Erschienen: 2015-07-27 00:00:00
ISSN
0300-8630

Zusammenfassung

The oncoprotein AF4-MLL has been shown to induce proB ALL in a murine model system, by using retroviral gene transfer into murine LSK cells and subsequent transplanation experiments into lethally irradiated mice. Leukemia development took about 6.5 month (Bursen et al., 2010). We also affinity-purified the AF4-MLL fusion protein complex and demonstrated its aberrant functions in vitro (hyperactive P-TEFb kinase, increased H3K4me3 and H3K79me3 signatures; Benedikt et al., 2011). Here, we will summarize our efforts to model AF4-MLL-mediated functions of in an in vitro model system, in order to trace the specific e…

Schlagworte

Work Klinische Pädiatrie