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An alternative splice process renders MLL either into an transcriptional activator or repressor

T Rössler, T Dingermann, R Marschalek · Klinische Pädiatrie · 2013 · Heft 05

Dokument
982086
CareLit-ID
Jahr
2013
Publikation
PDF
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Metadaten
DOI
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Bibliografische Angaben

Zeitschrift
Klinische Pädiatrie
Autor:innen
T Rössler, T Dingermann, R Marschalek
Ausgabe
Heft 05 / 2013
Seiten
–
Erschienen: 2013-05-22 00:00:00
ISSN
0300-8630

Zusammenfassung

We analyzed the biological properties of the MLL PHD1 – 3 domain. This domain is encoded by MLL exons 11 – 16 and localizes next to the Bromo-domain (MLL exons 17 – 19). We have identified 4 different splice variants that alter functions of the PHD domain 3, in particular its dimerization capacity and binding to CYP33 or H3K4me3. Binding to CYP33 allows to complex with BMI1, CBX4, HDAC and KDM 5B, and thus, to repress transcriptional processes. One out of 4 splice variants was able to bind CYP33, while others allow binding to H3K4me3 which in turn will enhance transcription. Of interest, MLL exon 11 encodes part…

Schlagworte

Klinische Pädiatrie