Department of Biosciences, Durham University, Durham DH1 3LE, UK.
National Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University, Wuhan 430070, China.
Development. 2023 Apr 1;150(7). doi: 10.1242/dev.201476. Epub 2023 Apr 5.
Plants respond to environmental stresses through controlled stem cell maintenance and meristem activity. One level of gene regulation is RNA alternative splicing. However, the mechanistic link between stress, meristem function and RNA splicing is poorly understood. The MERISTEM-DEFECTIVE (MDF) Arabidopsis gene encodes an SR-related family protein, required for meristem function and leaf vascularization, and is the likely orthologue of the human SART1 and yeast Snu66 splicing factors. MDF is required for the correct splicing and expression of key transcripts associated with root meristem function. We identified RSZ33 and ACC1, both known to regulate cell patterning, as splicing targets required for MDF function in the meristem. MDF expression is modulated by osmotic and cold stress, associated with differential splicing and specific isoform accumulation and shuttling between nucleus and cytosol, and acts in part via a splicing target SR34. We propose a model in which MDF controls splicing in the root meristem to promote stemness and to repress stress response, cell differentiation and cell death pathways.
植物通过控制干细胞的维持和分生组织的活性来应对环境压力。基因调控的一个层面是 RNA 可变剪接。然而,应激、分生组织功能和 RNA 剪接之间的机制联系还知之甚少。拟南芥的 MERISTEM-DEFECTIVE (MDF) 基因编码一个与 SR 相关的家族蛋白,该蛋白对于分生组织功能和叶片脉管系统的形成是必需的,并且可能是人类 SART1 和酵母 Snu66 剪接因子的同源物。MDF 对于与根分生组织功能相关的关键转录物的正确剪接和表达是必需的。我们鉴定了 RSZ33 和 ACC1,它们都已知可以调节细胞模式,作为 MDF 在分生组织中发挥功能所需的剪接靶标。MDF 的表达受渗透和冷胁迫的调节,与差异剪接以及特定的同工型积累和核质穿梭有关,并通过剪接靶标 SR34 发挥部分作用。我们提出了一个模型,其中 MDF 控制根分生组织中的剪接,以促进干性并抑制应激反应、细胞分化和细胞死亡途径。