Sharp Josh S, Bechhofer David H
Department of Pharmacology and Biological Chemistry, Mount Sinai School of Medicine of New York University, Box 1603, 1 Gustave L. Levy Place, New York, NY 10029-6754, USA.
Mol Microbiol. 2005 Jul;57(2):484-95. doi: 10.1111/j.1365-2958.2005.04683.x.
Previous work showed that a 42-nucleotide sequence from an SP82 bacteriophage early RNA functions as a 5' mRNA stabilizer in Bacillus subtilis. Real-time reverse transcriptase polymerase chain reaction (RT-PCR) analysis of decay of a model mRNA with alterations at the 5'-end was used to elucidate the mechanism of SP82-mediated stability. A predicted 5'-terminal stem-loop structure was essential for stabilization. Increasing the strength of the 5'-terminal structure above a minimum level did not result in increased stability. A thorough analysis of the context in which the stabilizing structure occurred included the effects of distance from 5'-end, translation of downstream coding sequence, and distance between the secondary structure and the ribosome binding site. Our data are consistent with the dominant mRNA decay pathway in B. subtilis being 5'-end dependent.
先前的研究表明,来自SP82噬菌体早期RNA的一段42个核苷酸的序列在枯草芽孢杆菌中作为5'端mRNA稳定剂发挥作用。利用实时逆转录聚合酶链反应(RT-PCR)对5'端发生改变的模型mRNA的衰变进行分析,以阐明SP82介导的稳定性机制。预测的5'端茎环结构对于稳定性至关重要。将5'端结构的强度提高到最低水平以上并不会导致稳定性增加。对稳定结构出现的背景进行的全面分析包括距5'端的距离、下游编码序列的翻译以及二级结构与核糖体结合位点之间的距离的影响。我们的数据与枯草芽孢杆菌中主要的mRNA衰变途径是5'端依赖性的这一观点一致。