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蛋白质精氨酸甲基转移酶6增强脊髓延髓性肌萎缩症中多聚谷氨酰胺扩展的雄激素受体功能及毒性。

Protein arginine methyltransferase 6 enhances polyglutamine-expanded androgen receptor function and toxicity in spinal and bulbar muscular atrophy.

作者信息

Scaramuzzino Chiara, Casci Ian, Parodi Sara, Lievens Patricia M J, Polanco Maria J, Milioto Carmelo, Chivet Mathilde, Monaghan John, Mishra Ashutosh, Badders Nisha, Aggarwal Tanya, Grunseich Christopher, Sambataro Fabio, Basso Manuela, Fackelmayer Frank O, Taylor J Paul, Pandey Udai Bhan, Pennuto Maria

机构信息

Department of Neuroscience and Brain Technologies, Istituto Italiano di Tecnologia, 16163 Genoa, Italy.

Department of Pediatrics, Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh, PA 15261, USA; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.

出版信息

Neuron. 2015 Jan 7;85(1):88-100. doi: 10.1016/j.neuron.2014.12.031.

Abstract

Polyglutamine expansion in androgen receptor (AR) is responsible for spinobulbar muscular atrophy (SBMA) that leads to selective loss of lower motor neurons. Using SBMA as a model, we explored the relationship between protein structure/function and neurodegeneration in polyglutamine diseases. We show here that protein arginine methyltransferase 6 (PRMT6) is a specific co-activator of normal and mutant AR and that the interaction of PRMT6 with AR is significantly enhanced in the AR mutant. AR and PRMT6 interaction occurs through the PRMT6 steroid receptor interaction motif, LXXLL, and the AR activating function 2 surface. AR transactivation requires PRMT6 catalytic activity and involves methylation of arginine residues at Akt consensus site motifs, which is mutually exclusive with serine phosphorylation by Akt. The enhanced interaction of PRMT6 and mutant AR leads to neurodegeneration in cell and fly models of SBMA. These findings demonstrate a direct role of arginine methylation in polyglutamine disease pathogenesis.

摘要

雄激素受体(AR)中的聚谷氨酰胺扩增是导致脊髓延髓肌肉萎缩症(SBMA)的原因,该疾病会导致下运动神经元的选择性丧失。我们以SBMA为模型,探讨了聚谷氨酰胺疾病中蛋白质结构/功能与神经退行性变之间的关系。我们在此表明,蛋白质精氨酸甲基转移酶6(PRMT6)是正常和突变型AR的特异性共激活因子,并且在AR突变体中PRMT6与AR的相互作用显著增强。AR和PRMT6通过PRMT6类固醇受体相互作用基序LXXLL以及AR激活功能2表面发生相互作用。AR反式激活需要PRMT6的催化活性,并且涉及Akt共有位点基序处精氨酸残基的甲基化,这与Akt介导的丝氨酸磷酸化相互排斥。PRMT6与突变型AR之间增强的相互作用会导致SBMA细胞和果蝇模型中的神经退行性变。这些发现证明了精氨酸甲基化在聚谷氨酰胺疾病发病机制中的直接作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34c8/4305189/36832c272be6/gr1.jpg

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