Biamonti Giuseppe, Maita Lucia, Montecucco Alessandra
Istituto di Genetica Molecolare, Consiglio Nazionale delle Ricerche, Pavia, Italy.
Front Oncol. 2018 Sep 26;8:408. doi: 10.3389/fonc.2018.00408. eCollection 2018.
Alternative splicing is a pervasive mechanism that molds the transcriptome to meet cell and organism needs. However, how this layer of gene expression regulation is coordinated with other aspects of the cell metabolism is still largely undefined. Glucose is the main energy and carbon source of the cell. Not surprisingly, its metabolism is finely tuned to satisfy growth requirements and in response to nutrient availability. A number of studies have begun to unveil the connections between glucose metabolism and splicing programs. Alternative splicing modulates the ratio between M1 and M2 isoforms of pyruvate kinase in this way determining the choice between aerobic glycolysis and complete glucose oxidation in the Krebs cycle. Reciprocally, intermediates in the Krebs cycle may impact splicing programs at different levels by modulating the activity of 2-oxoglutarate-dependent oxidases. In this review we discuss the molecular mechanisms that coordinate alternative splicing programs with glucose metabolism, two aspects with profound implications in human diseases.
可变剪接是一种普遍存在的机制,它塑造转录组以满足细胞和生物体的需求。然而,这一层基因表达调控如何与细胞代谢的其他方面协调,在很大程度上仍不明确。葡萄糖是细胞的主要能量和碳源。毫不奇怪,其代谢被精细调节以满足生长需求并响应营养物质的可用性。一些研究已经开始揭示葡萄糖代谢与剪接程序之间的联系。可变剪接以这种方式调节丙酮酸激酶M1和M2同工型之间的比例,从而决定有氧糖酵解和三羧酸循环中完全葡萄糖氧化之间的选择。相反,三羧酸循环中的中间产物可能通过调节2-氧代戊二酸依赖性氧化酶的活性,在不同水平上影响剪接程序。在这篇综述中,我们讨论了协调可变剪接程序与葡萄糖代谢的分子机制,这两个方面在人类疾病中具有深远影响。