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Early down-regulation of c-myc in dimethylsulfoxide-induced mouse erythroleukemia (MEL) cells is mediated at the P1/P2 promoters.

Oncogene 8, 1099-1102 (1993)
DOI
Open Access Green as soon as Postprint is submitted to ZB.
A block of RNA elongation in exon 1 of the murine c-myc gene has been described for normal mouse fibroblats, lymphoid and myeloid cell lines and mouse erythroleukemia (MEL) cells. MEL cells differentiate after induction with the chemical agent dimethylsulfoxide (DMSO). The rapid initial down-regulation of c-myc that occurs after treatment with DMSO has been explained by an increase in the block of RNA elongation within the 3′ part of c-myc exon 1. In contrast to these reports, we find that down-regulation of c-myc in DMSO-induced MEL cells occurs at the c-myc P1 and P2 promoters. The P1 promoter is repressed by inhibition of initiation, whereas transcription of P2 RNA is blocked by retention of RNA polymerase II at or close to the P2 promoter. The earlier described block of RNA elongation at a run of five thymidines in the 3′ part of c-myc exon 1 was not observed.
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Publication type Article: Journal article
Document type Scientific Article
ISSN (print) / ISBN 0950-9232
e-ISSN 0950-9232
Journal Oncogene
Quellenangaben Volume: 8, Issue: 4, Pages: 1099-1102 Article Number: , Supplement: ,
Publisher Nature Publishing Group
Reviewing status Peer reviewed