Woloschak M, Roberts J L
Dr. Arthur Fishberg Research Center for Neurobiology, Mount Sinai School of Medicine, New York, NY 10029, USA.
Biochem Biophys Res Commun. 1995 May 16;210(2):281-7. doi: 10.1006/bbrc.1995.1658.
Upstream transcription start sites in the murine POMC gene were detected at -48, -113, and -134 by primer extension analysis of RNA derived from a murine pituitary (AtT20) cell line. By RNase protection assay, dexamethasone treatment of AtT20 cells was found to reduce levels of transcripts initiated from the major transcription start site, but had a less prominent effect levels of transcripts initiated upstream. Conversely, treatment with 8-bromo-cAMP was found to induce levels of POMC gene transcripts from the major start site and from upstream start sites at -113 and -134, but reduced transcript levels initiated at a start site at -48. Treatment with the phorbol ester PDBU had no significant effects on levels of transcripts originating from any of the transcription start sites. Chronic treatments with these agents did not alter the proportion of upstream transcripts to the total level of POMC mRNA.
通过对源自小鼠垂体(AtT20)细胞系的RNA进行引物延伸分析,在小鼠阿黑皮素原(POMC)基因中检测到上游转录起始位点位于-48、-113和-134处。通过核糖核酸酶保护分析发现,地塞米松处理AtT20细胞可降低从主要转录起始位点起始的转录本水平,但对上游起始的转录本水平影响较小。相反,发现用8-溴环磷腺苷(8-bromo-cAMP)处理可诱导从主要起始位点以及-113和-134处的上游起始位点起始的POMC基因转录本水平,但降低了在-48处起始位点起始的转录本水平。佛波酯PDBU处理对源自任何转录起始位点的转录本水平均无显著影响。用这些试剂进行长期处理并未改变上游转录本占POMC mRNA总水平的比例。