Clingman Carina C, Deveau Laura M, Hay Samantha A, Genga Ryan M, Shandilya Shivender M D, Massi Francesca, Ryder Sean P
Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, United States.
Elife. 2014 Jun 16;3:e02848. doi: 10.7554/eLife.02848.
Gene expression and metabolism are coupled at numerous levels. Cells must sense and respond to nutrients in their environment, and specialized cells must synthesize metabolic products required for their function. Pluripotent stem cells have the ability to differentiate into a wide variety of specialized cells. How metabolic state contributes to stem cell differentiation is not understood. In this study, we show that RNA-binding by the stem cell translation regulator Musashi-1 (MSI1) is allosterically inhibited by 18-22 carbon ω-9 monounsaturated fatty acids. The fatty acid binds to the N-terminal RNA Recognition Motif (RRM) and induces a conformational change that prevents RNA association. Musashi proteins are critical for development of the brain, blood, and epithelium. We identify stearoyl-CoA desaturase-1 as a MSI1 target, revealing a feedback loop between ω-9 fatty acid biosynthesis and MSI1 activity. We propose that other RRM proteins could act as metabolite sensors to couple gene expression changes to physiological state.
基因表达与代谢在多个层面相互关联。细胞必须感知并响应其周围环境中的营养物质,而特化细胞必须合成其功能所需的代谢产物。多能干细胞具有分化为多种特化细胞的能力。代谢状态如何影响干细胞分化尚不清楚。在本研究中,我们发现干细胞翻译调节因子Musashi-1(MSI1)的RNA结合受到18 - 22碳ω-9单不饱和脂肪酸的变构抑制。脂肪酸与N端RNA识别基序(RRM)结合并诱导构象变化,从而阻止RNA结合。Musashi蛋白对脑、血液和上皮的发育至关重要。我们鉴定出硬脂酰辅酶A去饱和酶-1为MSI1的靶点,揭示了ω-9脂肪酸生物合成与MSI1活性之间的反馈回路。我们提出,其他RRM蛋白可能作为代谢物传感器,将基因表达变化与生理状态联系起来。