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一种用于全面基因表达分析的具有定向cDNA克隆和链特异性cRNA合成的mRNA扩增程序。

An mRNA amplification procedure with directional cDNA cloning and strand-specific cRNA synthesis for comprehensive gene expression analysis.

作者信息

Ohtsuka Satoko, Iwase Katsuro, Kato Masaki, Seki Naohiko, Shimizu-Yabe Atsuko, Miyauchi Osamu, Sakao Eiko, Kanazawa Masaki, Yamamoto Shigenori, Kohno Yoichi, Takiguchi Masaki

机构信息

Department of Biochemistry and Genetics, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.

出版信息

Genomics. 2004 Oct;84(4):715-29. doi: 10.1016/j.ygeno.2004.06.012.

Abstract

We developed an integrated system suitable for comprehensive gene expression studies including construction and analysis of cDNA microarrays starting from a small amount of mRNA. We amplified total mRNA first as cDNA mixtures by polymerase chain reaction and then as strand-specific cRNA mixtures by in vitro transcription. These amplified cDNA and cRNA enabled determination of mRNA levels by hybridization analyses such as Southern, Northern, reverse-Northern macroarray, and cDNA microarray analyses, as well as construction of the cDNA library with a unidirectional cDNA insert. By using strand-specific cRNA derived from rat primary-cultured hepatocytes, we detected putative antisense transcripts for the metallothionein gene. cDNA microarray analysis for genes regulated by glucocorticoids and glucagon in the hepatocytes revealed that a number of genes involved in signal transduction and transcriptional regulation were up- or down-regulated. The present system is widely applicable to gene expression analysis with limited amounts of RNA samples.

摘要

我们开发了一个适用于全面基因表达研究的综合系统,包括从少量mRNA开始构建和分析cDNA微阵列。我们首先通过聚合酶链反应将总mRNA扩增为cDNA混合物,然后通过体外转录将其扩增为链特异性cRNA混合物。这些扩增的cDNA和cRNA能够通过杂交分析(如Southern、Northern、反向Northern宏阵列和cDNA微阵列分析)来测定mRNA水平,以及构建具有单向cDNA插入片段的cDNA文库。通过使用源自大鼠原代培养肝细胞的链特异性cRNA,我们检测到了金属硫蛋白基因的推定反义转录本。对肝细胞中受糖皮质激素和胰高血糖素调节的基因进行的cDNA微阵列分析表明,许多参与信号转导和转录调控的基因被上调或下调。本系统广泛适用于有限RNA样本的基因表达分析。

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