Lykke-Andersen Jens, Bennett Eric J
Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093.
J Cell Biol. 2014 Feb 17;204(4):467-76. doi: 10.1083/jcb.201311103.
The correct decoding of messenger RNAs (mRNAs) into proteins is an essential cellular task. The translational process is monitored by several quality control (QC) mechanisms that recognize defective translation complexes in which ribosomes are stalled on substrate mRNAs. Stalled translation complexes occur when defects in the mRNA template, the translation machinery, or the nascent polypeptide arrest the ribosome during translation elongation or termination. These QC events promote the disassembly of the stalled translation complex and the recycling and/or degradation of the individual mRNA, ribosomal, and/or nascent polypeptide components, thereby clearing the cell of improper translation products and defective components of the translation machinery.
将信使核糖核酸(mRNA)正确解码为蛋白质是一项基本的细胞任务。翻译过程由多种质量控制(QC)机制监控,这些机制可识别有缺陷的翻译复合物,其中核糖体在底物mRNA上停滞。当mRNA模板、翻译机器或新生多肽出现缺陷,在翻译延伸或终止过程中使核糖体停滞时,就会出现停滞的翻译复合物。这些质量控制事件会促使停滞的翻译复合物解体,以及单个mRNA、核糖体和/或新生多肽成分的循环利用和/或降解,从而清除细胞中不适当的翻译产物和翻译机器的缺陷成分。