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PMID: 1644290 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Myc family oncoproteins function through a common pathway to transform normal cells in culture: cross-interference by Max and trans-acting dominant mutants.

Genes & development ·Vol. 6 ·No. 8 ·1992-08-00 ·Pages 1480-92

Mukherjee B, Morgenbesser SD, DePinho RA

Abstract

The myc family of cellular oncogenes encodes three highly related nuclear phosphoproteins (c-Myc, N-Myc, and L-Myc) that are believed to function as sequence-specific transcription factors capable of regulating genes important in cellular growth and differentiation. Current evidence indicates that Myc family proteins exist as biologically active heterodimeric complexes in association with another helix-loop-helix leucine zipper phosphoprotein, Max. We have investigated the common and unique properties among the Myc family, as well as the physiological role of Max in the regulation of Myc family function. We demonstrate that trans-activation-incompetent mutants of one Myc family member can act in trans to dominantly suppress the cotransformation activities of all three Myc oncoproteins, indicating that the Myc family functions through common genetic elements in its cellular transformation pathways. Employing co-immunoprecipitation with either anti-Myc or anti-Max antibodies, we show that the transfected normal c-Myc, N-Myc, and L-Myc oncoproteins associate with the endogenous Max protein in REF transformants, indicating that the Max interaction represents at least one component common to Myc family function. In addition, we observed a striking reduction in Myc cotransformation activity when a Max expression construct was added to myc/ras co-transfections. We discuss these biological findings in the context of a proposed model for Myc/Max function and regulation in which Max serves as either an obligate partner in the Myc/Max transcriptional complex or as a repressor in the form of a transcriptionally inert Max/Max homodimer capable of occupying Myc/Max-responsive gene targets.

Related Genes
MeSH Terms
Basic-Leucine Zipper Transcription Factors Blotting, Northern Cell Transformation, Neoplastic/genetics,metabolism DNA-Binding Proteins/genetics,metabolism Gene Expression Regulation, Neoplastic/physiology Genes, myc/genetics Genes, ras/genetics Mutation/genetics Plasmids/genetics Precipitin Tests Proto-Oncogene Proteins c-myc/genetics,metabolism Transcription Factors
Chemicals
Basic-Leucine Zipper Transcription Factors DNA-Binding Proteins Myc associated factor X Proto-Oncogene Proteins c-myc Transcription Factors
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Mukherjee B
Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, New York 10461.
Morgenbesser S D
DePinho R A
Article Info
Journal
Genes & development
Abbr.
Genes Dev
ISSN
0890-9369
Published
1992-08-00
Pages
1480-92
Language
English
Region
United States
NLM ID
8711660
Subset
IM
Grants
NCI NIH HHS · CA09173-14 · United States
NEI NIH HHS · R01 EY09300-01 · United States
NICHD NIH HHS · R01 HD28317-01 · United States
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