Department of Molecular Biology and Genetics, Howard Hughes Medical Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Department of Molecular Biology and Genetics, Howard Hughes Medical Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Mol Cell. 2021 Apr 1;81(7):1372-1383. doi: 10.1016/j.molcel.2021.02.022. Epub 2021 Mar 12.
Eukaryotic cells integrate multiple quality control (QC) responses during protein synthesis in the cytoplasm. These QC responses are signaled by slow or stalled elongating ribosomes. Depending on the nature of the delay, the signal may lead to translational repression, messenger RNA decay, ribosome rescue, and/or nascent protein degradation. Here, we discuss how the structure and composition of an elongating ribosome in a troubled state determine the downstream quality control pathway(s) that ensue. We highlight the intersecting pathways involved in RNA decay and the crosstalk that occurs between RNA decay and ribosome rescue.
真核细胞在细胞质中整合了多种蛋白质合成过程中的质量控制(QC)反应。这些 QC 反应由缓慢或停滞的延伸核糖体发出信号。根据延迟的性质,该信号可能导致翻译抑制、信使 RNA 降解、核糖体救援和/或新生蛋白质降解。在这里,我们讨论了处于困境中的延伸核糖体的结构和组成如何决定随后的质量控制途径。我们强调了 RNA 降解所涉及的交叉途径以及 RNA 降解和核糖体救援之间发生的串扰。