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拟南芥中转录本标准化的优质参考基因的全基因组鉴定与测试

Genome-wide identification and testing of superior reference genes for transcript normalization in Arabidopsis.

作者信息

Czechowski Tomasz, Stitt Mark, Altmann Thomas, Udvardi Michael K, Scheible Wolf-Rüdiger

机构信息

Max-Planck Institute of Molecular Plant Physiology, Potsdam, Germany.

出版信息

Plant Physiol. 2005 Sep;139(1):5-17. doi: 10.1104/pp.105.063743.

Abstract

Gene transcripts with invariant abundance during development and in the face of environmental stimuli are essential reference points for accurate gene expression analyses, such as RNA gel-blot analysis or quantitative reverse transcription-polymerase chain reaction (PCR). An exceptionally large set of data from Affymetrix ATH1 whole-genome GeneChip studies provided the means to identify a new generation of reference genes with very stable expression levels in the model plant species Arabidopsis (Arabidopsis thaliana). Hundreds of Arabidopsis genes were found that outperform traditional reference genes in terms of expression stability throughout development and under a range of environmental conditions. Most of these were expressed at much lower levels than traditional reference genes, making them very suitable for normalization of gene expression over a wide range of transcript levels. Specific and efficient primers were developed for 22 genes and tested on a diverse set of 20 cDNA samples. Quantitative reverse transcription-PCR confirmed superior expression stability and lower absolute expression levels for many of these genes, including genes encoding a protein phosphatase 2A subunit, a coatomer subunit, and an ubiquitin-conjugating enzyme. The developed PCR primers or hybridization probes for the novel reference genes will enable better normalization and quantification of transcript levels in Arabidopsis in the future.

摘要

在发育过程中以及面对环境刺激时丰度不变的基因转录本,是进行准确基因表达分析(如RNA凝胶印迹分析或定量逆转录-聚合酶链反应(PCR))的重要参考点。来自Affymetrix ATH1全基因组基因芯片研究的大量数据,为在模式植物拟南芥(Arabidopsis thaliana)中鉴定新一代表达水平非常稳定的参考基因提供了方法。研究发现,数百个拟南芥基因在整个发育过程以及一系列环境条件下,其表达稳定性优于传统参考基因。其中大多数基因的表达水平远低于传统参考基因,这使得它们非常适合用于在广泛的转录本水平上对基因表达进行标准化。针对22个基因设计并开发了特异性高效引物,并在20个不同的cDNA样本上进行了测试。定量逆转录-PCR证实,其中许多基因具有优异的表达稳定性和较低的绝对表达水平,包括编码蛋白磷酸酶2A亚基、外被体亚基和泛素结合酶的基因。为这些新型参考基因开发的PCR引物或杂交探针,将有助于未来更好地对拟南芥中的转录本水平进行标准化和定量分析。

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