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用于基因表达定量和定性分析的大规模cDNA测序

Large scale cDNA sequencing for analysis of quantitative and qualitative aspects of gene expression.

作者信息

Okubo K, Hori N, Matoba R, Niiyama T, Fukushima A, Kojima Y, Matsubara K

机构信息

Institute for Molecular and Cellular Biology, Osaka University, Japan.

出版信息

Nat Genet. 1992 Nov;2(3):173-9. doi: 10.1038/ng1192-173.

Abstract

Large scale sequencing of cDNAs provides a complementary approach to structural analysis of the human genome by generating expressed sequence tags (ESTs). We have initiated the large-scale sequencing of a 3'-directed cDNA library from the human liver cell line HepG2, that is a non-biased representation of the mRNA population. 982 random cDNA clones were sequenced yielding more than 270 kilobases. A significant portion of the identified genes encoded secretable proteins and components for protein-synthesis. The abundance of cDNA species varied from 2.2% to less than 0.004%. Fifty two percent of the mRNA were abundant species consisting of 173 genes and the rest were non-abundant, consisting of about 6,600 genes.

摘要

通过生成表达序列标签(EST),大规模cDNA测序为人类基因组的结构分析提供了一种互补方法。我们已经启动了对来自人肝癌细胞系HepG2的3'端定向cDNA文库的大规模测序,该文库是mRNA群体的无偏向性代表。对982个随机cDNA克隆进行了测序,产生了超过270千碱基的序列。所鉴定基因的很大一部分编码可分泌蛋白和蛋白质合成成分。cDNA种类的丰度从2.2%到小于0.004%不等。52%的mRNA是由173个基因组成的丰富种类,其余是非丰富种类,约由6600个基因组成。

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