Validation and structural characterization of the LEDGF/p75-MLL interface as a new target for the treatment of MLL-dependent leukemia
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25082813
DOI
10.1158/0008-5472.can-13-3602
PII: 0008-5472.CAN-13-3602
Knihovny.cz E-zdroje
- MeSH
- akutní myeloidní leukemie genetika metabolismus MeSH
- cílená molekulární terapie MeSH
- fúzní onkogenní proteiny genetika metabolismus MeSH
- histonlysin-N-methyltransferasa chemie genetika metabolismus MeSH
- HIV-integrasa chemie metabolismus MeSH
- lidé MeSH
- magnetická rezonanční spektroskopie MeSH
- mezibuněčné signální peptidy a proteiny chemie genetika metabolismus MeSH
- MFC-7 buňky MeSH
- molekulární modely MeSH
- myši MeSH
- protoonkogenní protein MLL chemie genetika metabolismus MeSH
- vazba proteinů MeSH
- vazebná místa MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- fúzní onkogenní proteiny MeSH
- histonlysin-N-methyltransferasa MeSH
- HIV-integrasa MeSH
- KMT2A protein, human MeSH Prohlížeč
- Kmt2a protein, mouse MeSH Prohlížeč
- lens epithelium-derived growth factor MeSH Prohlížeč
- mezibuněčné signální peptidy a proteiny MeSH
- protoonkogenní protein MLL MeSH
Mixed lineage leukemia (MLL) fusion-driven acute leukemias represent a genetically distinct subset of leukemias with poor prognosis. MLL forms a ternary complex with the lens epithelium-derived growth factor (LEDGF/p75) and MENIN. LEDGF/p75, a chromatin reader recognizing H3K36me3 marks, contributes to the association of the MLL multiprotein complex to chromatin. Formation of this complex is critical for the development of MLL leukemia. Available X-ray data represent only a partial structure of the LEDGF/p75-MLL-MENIN complex. Using nuclear magnetic resonance spectroscopy, we identified an additional LEDGF/p75-MLL interface, which overlaps with the binding site of known LEDGF/p75 interactors-HIV-1 integrase, PogZ, and JPO2. Binding of these proteins or MLL to LEDGF/p75 is mutually exclusive. The resolved structure, as well as mutational analysis, shows that the interaction is primarily sustained via two aromatic residues of MLL (F148 and F151). Colony-forming assays in MLL-AF9(+) leukemic cells expressing MLL interaction-defective LEDGF/p75 mutants revealed that this interaction is essential for transformation. Finally, we show that the clonogenic growth of primary murine MLL-AF9-expressing leukemic blasts is selectively impaired upon overexpression of a LEDGF/p75-binding cyclic peptide CP65, originally developed to inhibit the LEDGF/p75-HIV-1 integrase interaction. The newly defined protein-protein interface therefore represents a new target for the development of therapeutics against LEDGF/p75-dependent MLL fusion-driven leukemic disorders. Cancer Res; 74(18); 5139-51. ©2014 AACR.
Citace poskytuje Crossref.org
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