Jiang Z H, Wu J Y
Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Proc Soc Exp Biol Med. 1999 Feb;220(2):64-72. doi: 10.1046/j.1525-1373.1999.d01-11.x.
Programmed cell death (PCD) is critical for development and homeostasis of multicellular organisms. Genetic and biochemical studies have revealed that PCD is under complex and delicate regulation. An important level of such regulation may be pre-mRNA splicing as suggested by the observation that a number of PCD regulatory genes are expressed as functionally distinct or even antagonistic isoforms as a result of alternative splicing. Studies on alternative splicing of these genes are reviewed here. Expression and function of a large number of genes involved in PCD are regulated by alternative splicing, including death receptors and intracellular components of the death machinery. Alternative splicing affects not only intracellular distribution but also functional activity of these death regulators, providing a fine-tuning mechanism in modulating a presumably tightly controlled process of cell death.
程序性细胞死亡(PCD)对于多细胞生物体的发育和内环境稳定至关重要。遗传学和生物化学研究表明,PCD受到复杂而精细的调控。正如观察结果所暗示的,这种调控的一个重要层面可能是前体mRNA剪接,即由于可变剪接,许多PCD调控基因以功能不同甚至相互拮抗的异构体形式表达。本文综述了这些基因可变剪接的研究。大量参与PCD的基因的表达和功能受可变剪接调控,包括死亡受体和死亡机制的细胞内成分。可变剪接不仅影响这些死亡调节因子的细胞内分布,还影响其功能活性,为调节可能受到严格控制的细胞死亡过程提供了一种微调机制。