Das Subhadeep, Sarkar Debasish, Das Biswadip
Department of Life Science and Biotechnology, Jadavpur University, Kolkata, India.
Present Address: Laboratory of Molecular Genetics, Wadsworth Center, New York State Department of Health, Albany, NY 12201-2002, USA.
Microb Cell. 2017 Jul 3;4(7):212-228. doi: 10.15698/mic2017.07.580.
The cellular transcriptome is shaped by both the rates of mRNA synthesis in the nucleus and mRNA degradation in the cytoplasm under a specified condition. The last decade witnessed an exciting development in the field of post-transcriptional regulation of gene expression which underscored a strong functional coupling between the transcription and mRNA degradation. The functional integration is principally mediated by a group of specialized promoters and transcription factors that govern the stability of their cognate transcripts by "marking" them with a specific factor termed "coordinator." The "mark" carried by the message is later decoded in the cytoplasm which involves the stimulation of one or more mRNA-decay factors, either directly by the "coordinator" itself or in an indirect manner. Activation of the decay factor(s), in turn, leads to the alteration of the stability of the marked message in a selective fashion. Thus, the integration between mRNA synthesis and decay plays a potentially significant role to shape appropriate gene expression profiles during cell cycle progression, cell division, cellular differentiation and proliferation, stress, immune and inflammatory responses, and may enhance the rate of biological evolution.
细胞转录组由特定条件下细胞核中mRNA合成速率和细胞质中mRNA降解速率共同塑造。过去十年见证了基因表达转录后调控领域令人兴奋的发展,这突出了转录与mRNA降解之间强大的功能耦合。这种功能整合主要由一组特殊的启动子和转录因子介导,它们通过用一种称为“协调因子”的特定因子“标记”同源转录本,来控制其稳定性。转录本携带的“标记”随后在细胞质中被解码,这涉及直接由“协调因子”本身或以间接方式刺激一种或多种mRNA衰变因子。衰变因子的激活进而以选择性方式导致被标记转录本稳定性的改变。因此,mRNA合成与衰变之间的整合在细胞周期进程、细胞分裂、细胞分化与增殖、应激、免疫和炎症反应过程中塑造适当的基因表达谱方面可能发挥潜在的重要作用,并且可能提高生物进化速率。