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PMID: 1497918 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Myc and Max: a putative transcriptional complex in search of a cellular target.

Current opinion in cell biology ·Vol. 4 ·No. 3 ·1992-06-00 ·Pages 468-74

Torres R, Schreiber-Agus N, Morgenbesser SD, DePinho RA

Abstract

Biochemical and genetic observations have supported the hypothesis that Myc family proteins function to regulate genes important in cellular growth and differentiation. The recent findings that Myc proteins can associate with other cellular proteins, possess sequence-specific DNA-binding activity and may directly transactivate transcription of several candidate genes have provided an experimental framework in which to test the transcription factor model. Based on principles established for several well characterized viral oncoproteins, a model is presented in which the regulation of Myc function is controlled by specific cellular protein interactions that serve to activate or repress transactivation activity or deny access of the Myc complex to its target sequences.

Related Genes
MeSH Terms
Animals Base Sequence Basic-Leucine Zipper Transcription Factors DNA/genetics,metabolism DNA-Binding Proteins/genetics,metabolism Models, Biological Molecular Sequence Data Proto-Oncogene Proteins c-myc/genetics,metabolism Transcription Factors/genetics,metabolism Transcription, Genetic
Chemicals
Basic-Leucine Zipper Transcription Factors DNA-Binding Proteins Myc associated factor X Proto-Oncogene Proteins c-myc Transcription Factors DNA
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Torres R
Departments of Microbiology, Albert Einstein College of Medicine, Bronx, New York 10461.
Schreiber-Agus N
Morgenbesser S D
DePinho R A
Article Info
Journal
Current opinion in cell biology
Abbr.
Curr Opin Cell Biol
ISSN
0955-0674
Published
1992-06-00
Pages
468-74
Language
English
Region
England
NLM ID
8913428
Subset
IM
Grants
NCI NIH HHS · CA09173-14 · United States
NEI NIH HHS · R01 EY09300-01 · United States
NIGMS NIH HHS · T32 GM07128 · United States
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