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去除一种mRNA不稳定元件与原癌基因fos致癌性增加相关。

Removal of an mRNA destabilizing element correlates with the increased oncogenicity of proto-oncogene fos.

作者信息

Raymond V, Atwater J A, Verma I M

机构信息

Molecular Biology and Virology Laboratory, Salk Institute, San Diego, California 92138.

出版信息

Oncogene Res. 1989;5(1):1-12.

PMID:2506502
Abstract

AU-sequence motifs present in the 3' untranslated region (UTR) of many rapidly inducible messenger RNAs have been proposed to mediate their selective degradation. We have analyzed by quantitative nuclease S1 analysis the mRNA decay-rates of viral (v)/c-fos deletion mutants following transfection in a transient assay system. A 67 nucleotide mRNA destabilizing element, encompassing three conserved AUUUA motifs, was identified in the c-fos 3' UTR. The transforming ability of several v/c-fos recombinants correlates with the removal of the AU-rich sequence. Insertion of a c-fos DNA fragment containing the destabilizing element into the alpha-globin 3' UTR confers high instability to the otherwise stable alpha-globin mRNA. We conclude that a major parameter of oncogenicity by the c-fos gene is predicated by the presence or absence of AT-rich sequences located in the 3' non-coding region.

摘要

许多快速诱导型信使核糖核酸(mRNA)的3'非翻译区(UTR)中存在的AU序列基序被认为可介导其选择性降解。我们通过定量核酸酶S1分析,在瞬时分析系统中转染后分析了病毒(v)/c-fos缺失突变体的mRNA衰减率。在c-fos 3'UTR中鉴定出一个67个核苷酸的mRNA不稳定元件,其包含三个保守的AUUUA基序。几种v/c-fos重组体的转化能力与富含AU序列的去除相关。将含有不稳定元件的c-fos DNA片段插入α-珠蛋白3'UTR中,会使原本稳定的α-珠蛋白mRNA具有高度不稳定性。我们得出结论,c-fos基因致癌性的一个主要参数取决于3'非编码区中富含AT序列的存在与否。

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