Ozbulut Hasan Can, Hilgers Valérie
Max-Planck-Institute of Immunobiology and Epigenetics, Freiburg, Germany.
Faculty of Biology, Albert Ludwig University, Freiburg, Germany.
Front Mol Neurosci. 2024 Aug 1;17:1426410. doi: 10.3389/fnmol.2024.1426410. eCollection 2024.
In the nervous system, alternative RNA processing is particularly prevalent, which results in the expression of thousands of transcript variants found in no other tissue. Neuron-specific RNA-binding proteins co-transcriptionally regulate alternative splicing, alternative polyadenylation, and RNA editing, thereby shaping the RNA identity of nervous system cells. Recent evidence suggests that interactions between RNA-binding proteins and cis-regulatory elements such as promoters and enhancers play a role in the determination of neuron-specific expression profiles. Here, we discuss possible mechanisms through which transcription and RNA processing cross-talk to generate the uniquely complex neuronal transcriptome, with a focus on alternative 3'-end formation.
在神经系统中,可变RNA加工尤为普遍,这导致了数千种转录变体的表达,而这些变体在其他组织中并未发现。神经元特异性RNA结合蛋白在转录过程中共同调节可变剪接、可变多聚腺苷酸化和RNA编辑,从而塑造神经系统细胞的RNA特性。最近的证据表明,RNA结合蛋白与顺式调控元件(如启动子和增强子)之间的相互作用在神经元特异性表达谱的确定中发挥作用。在这里,我们讨论转录和RNA加工相互作用以产生独特复杂的神经元转录组的可能机制,重点是可变3'端形成。