| Literature DB >> 2468569 |
M Piechaczyk1, J M Blanchard, A Bonnieu, P Fort, N Mechti, J Rech, M Cuny, L Marty, F Ferré, B Lebleu.
Abstract
Proto-oncogenes c-myc and c-fos are subjected to a complex set of controls operating both at the transcriptional and post-transcriptional levels. We report here that: (i) antisense transcription occurs at the murine c-myc locus. However, its biological significance remains to be established; (ii) transcription of both genes is regulated in various situations by a block to elongation of nascent RNA chains. In the case of c-myc, the blockade involves a RNA structure whose nature remains unknown; (iii) elements responsible for the high degree of instability of c-myc and c-fos mRNAs reside in their 3' non-coding regions. A U-rich region, reminiscent of that present in the granulocyte-monocyte colony-stimulating factor mRNA destabilizer, is likely to be involved in the rapid degradation of c-fos mRNA; (iv) exon 1 substitution by intron 1-derived sequences lessens or negates the effect of the 3' destabilizer in abnormal c-myc RNAs from Burkitt's lymphomas and mouse plasmacytomas.Entities:
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Year: 1988 PMID: 2468569 DOI: 10.1016/0378-1119(88)90154-0
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688