c-myc mRNA稳定性的顺式决定因素。

Enzyme Pub Date : 1990-01-01 DOI:10.1159/000468755
M D Cole, S E Mango
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引用次数: 19

摘要

c-myc信息的快速周转介导了mRNA的低基础水平和对转录变化的快速反应。主要的RNA不稳定性决定因子(RID序列)位于3'非翻译区(UTR),位于富含A和U残基的80碱基区域内。与RID序列被定位为重复AUUUA序列的粒细胞-巨噬细胞集落刺激因子(GM-CSF) mRNA相反,该序列在c-myc 3' UTR中唯一拷贝的突变对RNA转换没有影响。因此,c-myc RID序列似乎与GM-CSF的序列大不相同,这可能解释了这些mrna对半衰期的不同调节。由于翻译抑制剂稳定了c-myc mRNA,因此c-myc mRNA的周转也与翻译紧密耦合。起始AUG到终止密码子的突变稳定了c-myc RNA,认为装载多聚体(可能伴随着在细胞骨架上的定位)也是适当的信息周转所必需的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
cis-acting determinants of c-myc mRNA stability.

Rapid turnover of the c-myc message mediates both the low basal level of mRNA and the rapid response to changes in transcription. The primary RNA instability determinant (RID sequence) resides in the 3' untranslated region (UTR), within an 80 base region that is rich in A and U residues. In contrast to granulocyte-macrophage colony-stimulating factor (GM-CSF) mRNA in which the RID sequence has been mapped to a repeating AUUUA sequence, mutation of the only copy of this sequence in the c-myc 3' UTR has no effect on RNA turnover. Thus the c-myc RID sequence appears to be quite different from that of GM-CSF, which may account for the differential regulation of half-life exhibited by these mRNAs. c-myc mRNA turnover is also tightly coupled to translation since translational inhibitors stabilize this mRNA. Mutation of the initiating AUG to a termination codon stabilizes c-myc RNA, arguing that loading with polysomes (perhaps accompanied by localization on the cytoskeleton) is also required for proper message turnover.

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