Induction of a Secreted Protein by the Myxoid Liposarcoma Oncogene

The TLS-CHOP oncoprotein, found in the majority of human myxoid liposarcomas, consists of a fusion between the transcription factor CHOP/GADD153 and the N terminus of an RNA-binding protein TLS/FUS. Clinical correlation and in vitro transformation assays indicate that the N terminus of TLS plays an...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 1999-04, Vol.96 (9), p.5025-5030
Hauptverfasser: Kuroda, Masahiko, Wang, XiaoZhong, Sok, John, Yin Yin, Chung, Peter, Giannotti, JoAnn W., Jacobs, Kenneth A., Fitz, Lori J., Murtha-Riel, Patricia, Turner, Katherine J., Ron, David
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Sprache:eng
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Zusammenfassung:The TLS-CHOP oncoprotein, found in the majority of human myxoid liposarcomas, consists of a fusion between the transcription factor CHOP/GADD153 and the N terminus of an RNA-binding protein TLS/FUS. Clinical correlation and in vitro transformation assays indicate that the N terminus of TLS plays an important role in oncogenesis by TLS-CHOP. Until now, however, the only activity attributed to the oncoprotein is that of inhibiting the binding of transcription factors of the C/EBP class to certain adipogenic target genes, a function that TLS-CHOP shares with the nononcogenic CHOP protein. Here we report the isolation of a gene, DOL54, that is activated in primary fibroblasts by the expression of TLS-CHOP. DOL54 is expressed in the neoplastic component of human myxoid liposarcomas and increases the tumorigenicity of cells injected in nude mice. Activation of DOL54 requires an intact DNA-binding and dimerization domain in TLS-CHOP, a suitable cellular dimerization partner, and depends on the TLS N terminus. Normal adipocytic differentiation is associated with an early and transient expression of DOL54, and the gene encodes a secreted protein that is tightly associated with the cell surface or extracellular matrix. TLS-CHOP thus leads to the unscheduled expression of a gene that is normally associated with adipocytic differentiation.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.96.9.5025