Cleveland D W, Yen T J
Department of Biological Chemistry, Johns Hopkins University, School of Medicine, Baltimore, MD 21205.
New Biol. 1989 Nov;1(2):121-6.
Regulated changes in mRNA stability play an important role in modulating the level of expression of many eukaryotic genes. In several systems, specific sequence determinants that dictate mRNA instability have been identified. Thus, the presence of instability determinants, and not the absence of sequences that dictate stability, appears to be required for regulated mRNA degradation. These instability determinants presumably interact with specific nucleases or other trans-acting factors that regulate the accessibility of the domain to nucleases. Although each RNA destabilization pathway has unique features, in many cases RNA degradation requires ongoing protein synthesis. In some of the systems discussed, the mRNAs are degraded co-translationally, perhaps by a ribosome-associated ribonuclease. For other messages, the mechanistic reasons for the dependence of mRNA degradation on ongoing protein synthesis are still unknown.
mRNA稳定性的调控变化在调节许多真核基因的表达水平中起着重要作用。在多个系统中,已鉴定出决定mRNA不稳定性的特定序列决定因素。因此,似乎是不稳定性决定因素的存在,而非决定稳定性的序列的缺失,是调控mRNA降解所必需的。这些不稳定性决定因素可能与特定核酸酶或其他反式作用因子相互作用,这些因子调节该结构域对核酸酶的可及性。尽管每种RNA去稳定化途径都有独特的特征,但在许多情况下,RNA降解需要持续的蛋白质合成。在讨论的一些系统中,mRNA在翻译过程中被降解,可能是由核糖体相关的核糖核酸酶降解。对于其他信息,mRNA降解依赖于持续蛋白质合成的机制原因仍然未知。