Comparing gene expression profiles in human liver, gastric, and pancreatic tissues using full-length-enriched cDNA libraries

被引:5
作者
Otsuka, M [1 ]
Arai, M
Mori, M
Kato, M
Kato, N
Yokosuka, O
Ochiai, T
Takiguchi, M
Omata, M
Seki, N
机构
[1] Univ Tokyo, Grad Sch Med, Dept Gastroenterol, Tokyo, Japan
[2] Chiba Univ, Grad Sch Med, Dept Med & Clin Oncol, Chiba, Japan
[3] Chiba Univ, Grad Sch Med, Acad Dept Surg, Chiba, Japan
[4] Chiba Univ, Grad Sch Med, Dept Biochem & Genet E1, Chiba, Japan
[5] Chiba Univ, Grad Sch Med, Dept Funct Genom, Chuo Ku, Chiba 2608670, Japan
关键词
gene profiling; full-length cDNA; oligo-capping; microarray;
D O I
10.1016/S1386-6346(03)00161-X
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
In the post-genome-sequencing era, full-length cDNA-sequence resources are extremely useful for functional analyses of genes. In addition, comprehensive gene profiling of human tissues at the mRNA level is also useful in understanding the molecular mechanisms of tissue-specific functions and disease pathogenesis. In this study, to obtain a wide variety of full-length cDNA clones derived from digestive tissues, numerous expressed sequence tags were generated from libraries enriched with full-length cDNAs. In total, 13 575 sequences were obtained from three cDNA libraries, which were constructed from tissues and cell lines of human liver, stomach, and pancreas. The integration of overlapping clones categorized the sequences into 5936 clusters (1666, 2746, and 2222 clusters in the liver, stomach, and pancreas, respectively). Of these, 1138 clones were scored as full-length cDNAs. Surprisingly, the redundant clones from all three tissues were assembled to show that only 101 genes (1.7% of the assembled 5936 genes) were shared. These results suggest that functional differences between tissues are probably related to their divergent gene expression profiles, and form a basis for understanding the molecular mechanisms underlying tissue-specific pathogenesis that are expressed in different organs. In addition, the full-length cDNAs obtained in this study should prove useful for future functional analyses of the genes expressed in digestive tissues. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:76 / 82
页数:7
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