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拟南芥全基因组Affymetrix探针阵列的开发与评估。

Development and evaluation of an Arabidopsis whole genome Affymetrix probe array.

作者信息

Redman Julia C, Haas Brian J, Tanimoto Gene, Town Christopher D

机构信息

The Institute for Genomic Research, 9712 Medical Center Drive, Rockville, MD 20850, USA.

出版信息

Plant J. 2004 May;38(3):545-61. doi: 10.1111/j.1365-313X.2004.02061.x.

Abstract

We describe the development of a high-density Arabidopsis'whole genome' oligonucleotide probe array for expression analysis (the Affymetrix ATH1 GeneChip probe array) that contains approximately 22 750 probe sets. Precedence on the array was given to genes for which either expression evidence or a credible database match existed. The remaining space was filled with 'hypothetical' genes. The new ATH1 array represents approximately 23 750 genes of which 60% were detected in RNA from cultured seedlings. Sensitivity of the array, determined using spiking controls, was approximately one transcript per cell. The array demonstrated high technical reproducibility and concordance with real-time PCR results. Indole-3 acetic acid (IAA)-induced changes in gene expression were used for biological validation of the array. A total of 222 genes were significantly upregulated and 103 significantly downregulated by exposure to IAA. Of the genes whose products could be functionally classified, the largest specific classes of upregulated genes were transcriptional regulators and protein kinases, many fewer of which were represented among the downregulated genes. Over one-third of the auxin-regulated genes have no known function, although many belong to gene families with members that have previously been shown to be auxin regulated. For the 6714 genes represented both on this and the earlier Arabidopsis Genome (AG) array, both signal intensities and gene expression ratios were very similar. Mapping of the oligonucleotides on the ATH1 array to the latest (version 4.0) annotation showed that over 95% of the probe sets (based on version 2.0 annotation) still fully represented their original target genes.

摘要

我们描述了一种用于表达分析的高密度拟南芥“全基因组”寡核苷酸探针阵列(Affymetrix ATH1基因芯片探针阵列)的开发,该阵列包含约22750个探针集。阵列上优先排布那些有表达证据或与可靠数据库匹配的基因。其余空间则用“假定”基因填充。新的ATH1阵列代表了约23750个基因,其中60%在培养幼苗的RNA中被检测到。使用加标对照确定的阵列灵敏度约为每个细胞一个转录本。该阵列显示出高技术重复性且与实时PCR结果一致。吲哚 - 3 - 乙酸(IAA)诱导的基因表达变化被用于该阵列的生物学验证。暴露于IAA后,共有222个基因显著上调,103个基因显著下调。在其产物可进行功能分类的基因中,上调基因中最大的特定类别是转录调节因子和蛋白激酶,而下调基因中这类基因较少。超过三分之一的生长素调节基因功能未知,尽管许多属于此前已显示受生长素调节的成员所在的基因家族。对于在此阵列和早期拟南芥基因组(AG)阵列上都有代表的6714个基因,信号强度和基因表达比率都非常相似。将ATH1阵列上的寡核苷酸映射到最新(4.0版)注释显示,超过95%的探针集(基于2.0版注释)仍能完全代表其原始靶基因。

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