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在哺乳动物细胞中,起始于第1内含子的c-myc mRNA与正常c-myc mRNA共存,且两种转录本具有相似的调控。

Coexistence of a c-myc mRNA initiated in intron 1 with the normal c-myc mRNA and similar regulation of both transcripts in mammalian cells.

作者信息

Ray D, Robert-Lézénès J

机构信息

INSERM U-248, Faculté de Médecine Lariboisière, Paris, France.

出版信息

Oncogene Res. 1989;5(1):73-8.

PMID:2674860
Abstract

We previously described a c-myc mRNA initiated within intron 1 at a major start site designated P3. This mRNA was observed in tumorigenic murine cells with no detectable rearrangement of the c-myc gene. In the present study, we report that P3 mRNA also coexists with the P1/P2 c-myc transcript in non-tumorigenic murine cell lines and that a c-myc mRNA which appears to be an equivalent of the murine P3 transcript is found in various rat and human cells. These data suggest that P3 represents a promoter of the normal, non-rearranged mammalian c-myc gene. Furthermore, both P1/P2 and P3 mRNA levels are similarly regulated by cycloheximide and by dimethylsulfoxide (DMSO) in murine erythroleukemia Friend cells.

摘要

我们之前描述过一种c-myc信使核糖核酸(mRNA),它起始于内含子1内一个被命名为P3的主要起始位点。在c-myc基因无可检测重排的致瘤性鼠细胞中观察到了这种mRNA。在本研究中,我们报告P3 mRNA也与P1/P2 c-myc转录本共存于非致瘤性鼠细胞系中,并且在各种大鼠和人类细胞中发现了一种似乎等同于鼠P3转录本的c-myc mRNA。这些数据表明P3代表正常的、未重排的哺乳动物c-myc基因的一个启动子。此外,在鼠红白血病Friend细胞中,P1/P2和P3 mRNA水平受环己酰亚胺和二甲基亚砜(DMSO)的调控方式相似。

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