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赤拟谷盗细胞系TcA:细胞生物学的新工具包。

The Tribolium castaneum cell line TcA: a new tool kit for cell biology.

作者信息

Silver Kristopher, Jiang Hongbo, Fu Jinping, Phillips Thomas W, Beeman Richard W, Park Yoonseong

机构信息

Department of Anatomy and Physiology, Kansas State University, Manhattan, KS 66506.

1] Department of Entomology, Kansas State University, Manhattan, KS 66506 [2] Key Laboratory of Entomology and Pest Control Engineering, College of Plant Protection, Southwest University, Chongqing 400715.

出版信息

Sci Rep. 2014 Oct 30;4:6840. doi: 10.1038/srep06840.

Abstract

The red flour beetle, Tribolium castaneum, is an agriculturally important insect pest that has been widely used as a model organism. Recently, an adherent cell line (BCIRL-TcA-CLG1 or TcA) was developed from late pupae of the red flour beetle. Next generation transcriptome sequencing of TcA cells demonstrated expression of a wide variety of genes associated with specialized functions in chitin metabolism, immune responses and cellular and systemic RNAi pathways. Accordingly, we evaluated the sensitivity of TcA cells to dsRNA to initiate an RNAi response. TcA cells were highly sensitive to minute amounts of dsRNA, with a minimum effective dose of 100 pg/mL resulting in significant suppression of gene expression. We have also developed a plasmid containing two TcA-specific promoters, the promoter from the 40S ribosomal protein subunit (TC006550) and a bi-directional heat shock promoter (TcHS70) from the intergenic space between heat shock proteins 68a and b. These promoters have been employed to provide high levels of either constitutive (TC006550) or inducible (TcHS70) gene expression of the reporter proteins. Our results show that the TcA cell line, with its sensitivity to RNAi and functional TcA-specific promoters, is an invaluable resource for studying basic molecular and physiological questions.

摘要

赤拟谷盗(Tribolium castaneum)是一种对农业具有重要影响的害虫,已被广泛用作模式生物。最近,从赤拟谷盗的晚期蛹中建立了一种贴壁细胞系(BCIRL-TcA-CLG1或TcA)。对TcA细胞进行的下一代转录组测序表明,多种与几丁质代谢、免疫反应以及细胞和全身RNA干扰途径中的特殊功能相关的基因得以表达。因此,我们评估了TcA细胞对双链RNA(dsRNA)引发RNA干扰反应的敏感性。TcA细胞对微量dsRNA高度敏感,最小有效剂量为100 pg/mL,可导致基因表达受到显著抑制。我们还构建了一个质粒,其中包含两个TcA特异性启动子,即来自40S核糖体蛋白亚基(TC006550)的启动子和来自热休克蛋白68a和b之间基因间隔区的双向热休克启动子(TcHS70)。这些启动子已被用于实现报告蛋白高水平的组成型(TC006550)或诱导型(TcHS70)基因表达。我们的结果表明,TcA细胞系因其对RNA干扰的敏感性和功能性TcA特异性启动子,是研究基本分子和生理学问题的宝贵资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd22/4213800/f8da97e72465/srep06840-f1.jpg

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