SAGE identification of gene transcripts with profiles unique to pluripotent mouse R1 embryonic stem cells

被引:76
作者
Anisimov, SV
Tarasov, KV
Tweedie, D
Stern, MD
Wobus, AM
Boheler, KR
机构
[1] NIA, NIH, Baltimore, MD 21224 USA
[2] Inst Plant Genet, D-06466 Gatersleben, Germany
关键词
embryonic stem cells; SAGE technique; Q-PCR; transcriptome; pluripotentiality; gene expression; gene profile;
D O I
10.1006/geno.2002.6687
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The identification of signals that regulate pluripotentiality and self-renewal is fundamental to the understanding of stem cell biology. To quantify the functionally active genome of pluripotent R1 embryonic stem (ES) cells, we used the method of serial analysis of gene expression (SAGE) to sequence a total of 140,313 SAGE tags. Of 44,569 unique transcripts, 9% matched known genes in the nonredundant GenBank database, whereas > 35% of the unique tags did not match any known mouse sequence. Comparisons of relatively abundant (greater than or equal to 20) tags in the ES cell SAGE catalog with publicly available SAGE data sets identified 16 transcripts with an abundance profile unique to pluripotent R1 ES cells. We confirmed 12 by RTPCR including those encoding KLF2, a transcription factor; galanin, a hypothalamic neurohormone; BAX, a proapoptotic signaling factor; and CDK4 and PAL31, cell cycle progression associated proteins. The data from this study provide a starting point for detailed transcriptome analyses of stem cells.
引用
收藏
页码:169 / 176
页数:8
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