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PMID: 1549358 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Three distinct elements within the murine c-myc promoter are required for transcription.

Oncogene ·Vol. 7 ·No. 3 ·1992-03-00 ·Pages 411-21

Moberg KH, Logan TJ, Tyndall WA, Hall DJ

Abstract

We have undertaken a detailed analysis of the cis-acting elements that are required for optimal transcription initiation from P2, the major promoter of the murine c-myc gene. We find that three elements contribute to promoter strength, termed ME1a2, E2F and ME1a1 at positions -85, -64 and -46 respectively (relative to P2). Individually the elements are weak, but combined they contribute to full promoter activity, all acting in a positive fashion. The E2F element is the site at which the SV40 large T antigen transactivates the c-myc promoter. However, transactivation requires the presence of the ME1a2 or ME1a1 elements in addition to E2F. By a number of criteria it appears that the ME1a2 and ME1a1 elements bind the same or a very closely related protein (monomer Mr 94,000). It was found that Hela cells contain a novel factor that is capable of binding to the ME1a1 and ME1a2 elements but only in the presence of the protein-dissociating agents deoxycholate or formamide. Finally, the E2F factor binds DNA both as a monomer and as a multiprotein complex; the latter is cell type specific. Both types of bound E2F factor form less stable protein-DNA complexes than the ME1a2/ME1a1 factor.

Related Genes
MeSH Terms
3T3 Cells Animals Antigens, Polyomavirus Transforming/genetics Base Sequence DNA-Binding Proteins/chemistry,metabolism Gene Expression Regulation Genes, myc HeLa Cells Humans Macromolecular Substances Mice Molecular Sequence Data Multiprotein Complexes Oligodeoxyribonucleotides/chemistry Promoter Regions, Genetic Regulatory Sequences, Nucleic Acid Sequence Alignment Transcription, Genetic Transcriptional Activation
Chemicals
Antigens, Polyomavirus Transforming DNA-Binding Proteins Macromolecular Substances Multiprotein Complexes Oligodeoxyribonucleotides
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Moberg K H
Department of Biochemistry and Molecular Biology, Thomas Jefferson University, Philadelphia, Pennsylvania 19107.
Logan T J
Tyndall W A
Hall D J
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
1992-03-00
Pages
411-21
Language
English
Region
England
NLM ID
8711562
Subset
IM
Grants
NCI NIH HHS · CA51170-01 · United States
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