Shimkets R A, Lowe D G, Tai J T, Sehl P, Jin H, Yang R, Predki P F, Rothberg B E, Murtha M T, Roth M E, Shenoy S G, Windemuth A, Simpson J W, Simons J F, Daley M P, Gold S A, McKenna M P, Hillan K, Went G T, Rothberg J M
CuraGen Corporation, 555 Long Wharf Drive, New Haven, CT 06511, USA.
Nat Biotechnol. 1999 Aug;17(8):798-803. doi: 10.1038/11743.
We describe an mRNA profiling technique for determining differential gene expression that utilizes, but does not require, prior knowledge of gene sequences. This method permits high-throughput reproducible detection of most expressed sequences with a sensitivity of greater than 1 part in 100,000. Gene identification by database query of a restriction endonuclease fingerprint, confirmed by competitive PCR using gene-specific oligonucleotides, facilitates gene discovery by minimizing isolation procedures. This process, called GeneCalling, was validated by analysis of the gene expression profiles of normal and hypertrophic rat hearts following in vivo pressure overload.
我们描述了一种用于确定差异基因表达的mRNA分析技术,该技术利用但不要求事先了解基因序列。这种方法能够以大于十万分之一的灵敏度对大多数表达序列进行高通量可重复检测。通过使用基因特异性寡核苷酸的竞争性PCR确认的限制性内切酶指纹数据库查询来鉴定基因,通过最小化分离程序促进了基因发现。这个过程称为基因调用,通过分析体内压力过载后正常和肥大大鼠心脏的基因表达谱进行了验证。