Identification of global alteration of translational regulation in glioma in vivo.

Identification of global alteration of translational regulation in glioma in vivo.
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DOI:
10.1371/journal.pone.0046965
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发表时间:
2012
期刊:
影响因子:
3.7
通讯作者:
Holland EC
Holland EC
中科院分区:
综合性期刊3区
文献类型:
--
作者:
Helmy K;Halliday J;Fomchenko E;Setty M;Pitter K;Hafemeister C;Holland EC

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基因表达的转录后调控有助于细胞的蛋白质输出,然而,缺乏用于测量复杂体内系统中的翻译调控的方法。在这里,我们描述了一种灵敏的方法,用于测量在定义的细胞群体在体内异质组织的翻译调控。我们采用翻译核糖体亲和纯化(TRAP)方法来测量在基因工程小鼠模型(GEM)胶质瘤中Olig 2阳性肿瘤细胞群体中翻译核糖体中单个mRNA转录物的相对占有率。对体内肿瘤细胞的配对核糖体结合和总细胞mRNA群体的总体测量确定了mRNA种类中相对核糖体占据的广泛分布,其在生物样品中具有高度可重复性。胶质瘤细胞与正常脑中未转化的少突胶质细胞祖细胞的翻译状态的比较确定了肿瘤中翻译的全局改变,特别是涉及细胞分裂和合成代谢的基因。此外,在失去PTEN(神经胶质瘤中最常突变和缺失的肿瘤抑制因子之一)后,对稳态翻译效率的改变的研究鉴定了参与细胞呼吸的蛋白质的差异翻译,其通过PI 3 K/Akt信号传导和细胞糖基化谱进行规范调节,已知其失调与肿瘤进展相关。将本文所述的翻译效率分析方法应用于其他生物背景和条件将扩展我们对这种重要的基因调控模式在复杂体内系统中的范围和影响的认识。
Post-transcriptional regulation of gene expression contributes to the protein output of a cell, however, methods for measuring translational regulation in complex in vivo systems are lacking. Here, we describe a sensitive method for measuring translational regulation in defined cell populations from heterogeneous tissue in vivo. We adapted the translating ribosome affinity purification (TRAP) methodology to measure the relative occupancy of individual mRNA transcripts in translating ribosomes in the Olig2-positive tumor cell population in a genetically engineered mouse model (GEM) of glioma. Global measurement of paired ribosome-bound and total cellular mRNA populations from tumor cells in vivo identified a broad distribution of relative ribosome occupancies amongst mRNA species that was highly reproducible across biological samples. Comparison of the translation state of glioma cells to non-transformed oligodendrocyte progenitor cells in normal brain identified global alteration of translation in tumor, and specifically of genes involved in cell division and synthetic metabolism. Furthermore, investigation of alteration in steady state translational efficiencies upon loss of PTEN, one of the most frequently mutated and deleted tumor suppressors in glioma, identified differential translation of proteins involved in cellular respiration, canonically regulated by PI3K/Akt signaling, and cellular glycosylation profiles, deregulation of which is known to be associated with tumor progression. Application of the translation efficiency profiling method described here to other biological contexts and conditions would extend our knowledge of the scope and impact of this important mode of gene regulation in complex in vivo systems.
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