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Srsf3 介导 PDGFRα 信号下游面部间充质中的选择性 RNA 剪接。

Srsf3 mediates alternative RNA splicing downstream of PDGFRα signaling in the facial mesenchyme.

机构信息

Department of Craniofacial Biology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.

RNA Bioscience Initiative, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.

出版信息

Development. 2021 Jul 15;148(14). doi: 10.1242/dev.199448. Epub 2021 Jul 13.

DOI:10.1242/dev.199448
PMID:34184034
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8313863/
Abstract

Signaling through the platelet-derived growth factor receptor alpha (PDGFRα) is crucial for mammalian craniofacial development, although the mechanisms by which the activity of downstream intracellular effectors is regulated to mediate gene expression changes have not been defined. We find that the RNA-binding protein Srsf3 is phosphorylated at Akt consensus sites downstream of PI3K-mediated PDGFRα signaling in mouse palatal mesenchyme cells, leading to its nuclear translocation. We further demonstrate that ablation of Srsf3 in the mouse neural crest lineage leads to facial clefting due to defective cranial neural crest cell proliferation and survival. Finally, we show that Srsf3 regulates the alternative RNA splicing of transcripts encoding protein kinases in the mouse facial process mesenchyme to regulate PDGFRα-dependent intracellular signaling. Collectively, our findings reveal that alternative RNA splicing is an important mechanism of gene expression regulation downstream of PI3K/Akt-mediated PDGFRα signaling in the facial mesenchyme and identify Srsf3 as a critical regulator of craniofacial development.

摘要

血小板衍生生长因子受体 α (PDGFRα) 的信号传递对于哺乳动物颅面部发育至关重要,尽管尚未确定下游细胞内效应物的活性如何调节以介导基因表达变化的机制。我们发现,在 PI3K 介导的 PDGFRα 信号转导下游,RNA 结合蛋白 Srsf3 在小鼠腭中胚层细胞中被 Akt 共识位点磷酸化,导致其核转位。我们进一步证明,在小鼠神经嵴谱系中敲除 Srsf3 会导致面部裂隙,这是由于颅神经嵴细胞增殖和存活缺陷所致。最后,我们表明 Srsf3 调节编码蛋白激酶的转录本在小鼠面部突间中胚层的选择性 RNA 剪接,以调节 PDGFRα 依赖性细胞内信号转导。总之,我们的研究结果表明,选择性 RNA 剪接是 PI3K/Akt 介导的 PDGFRα 信号转导下游在面部中胚层中基因表达调控的重要机制,并确定 Srsf3 是颅面部发育的关键调节因子。