Physical and functional link of the leukemia-associated factors AML1 and PML

The AML1-CBFβ transcription factor complex is the most frequent target of specific chromosome translocations in acute myeloid leukemia (AML). The promyelocytic leukemia (PML) gene is also frequently involved in AML-associated translocation. Here we report that a specific isoform PML I forms a comple...

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Veröffentlicht in:Blood 2005-01, Vol.105 (1), p.292-300
Hauptverfasser: Nguyen, Lan Anh, Pandolfi, Pier Paolo, Aikawa, Yukiko, Tagata, Yusuke, Ohki, Misao, Kitabayashi, Issay
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Sprache:eng
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Zusammenfassung:The AML1-CBFβ transcription factor complex is the most frequent target of specific chromosome translocations in acute myeloid leukemia (AML). The promyelocytic leukemia (PML) gene is also frequently involved in AML-associated translocation. Here we report that a specific isoform PML I forms a complex with AML1. PML I was able to recruit AML1 and coactivator p300 in PML nuclear bodies and enhance the AML1-mediated transcription in the presence of p300. A specific C-terminal region of PML I and a C-terminal region of AML1 were found to be required for both their association and colocalization in the nuclear bodies. Overexpression of PML I stimulates myeloid cells to differentiate. These results suggest that PML I could act as a mediator for AML1 and its coactivator p300/CBP to assemble into functional complexes and, consequently, activate AML1-dependent transcription and myeloid cell differentiation. (Blood. 2005;105:292-300)
ISSN:0006-4971
1528-0020
DOI:10.1182/blood-2004-03-1185