Linskens M H, Feng J, Andrews W H, Enlow B E, Saati S M, Tonkin L A, Funk W D, Villeponteau B
Geron Corporation, Menlo Park, CA 94025, USA.
Nucleic Acids Res. 1995 Aug 25;23(16):3244-51. doi: 10.1093/nar/23.16.3244.
Recently, a novel PCR-based technique, differential display (DD), has facilitated the study of differentially expressed genes at the mRNA level. We report here an improved version of DD, which we call Enhanced Differential Display (EDD). We have modified the technique to enhance reproducibility and to facilitate sequencing and cloning. Using EDD, we have generated and verified a catalog of genes that are differentially expressed between young and senescent human diploid fibroblasts (HDF). From 168 genetags that were identified initially, 84 could be sequenced directly from PCR amplified bands. These sequences represent 27 known genes and 37 novel genes. By Northern blot analysis we have confirmed the differential expression of a total of 23 genes (12 known, 11 novel), while 19 (seven known, 12 novel) did not show differential expression. Several of the known genes were previously observed by others to be differentially expressed between young and senescent fibroblasts, thereby validating the technique.
最近,一种基于聚合酶链反应(PCR)的新技术——差异显示(DD),推动了在mRNA水平上对差异表达基因的研究。我们在此报告一种改进版的DD,我们称之为增强差异显示(EDD)。我们对该技术进行了改良,以提高其可重复性,并便于进行测序和克隆。使用EDD,我们已生成并验证了一份在年轻和衰老的人二倍体成纤维细胞(HDF)之间差异表达的基因目录。从最初鉴定出的168个基因标签中,有84个可以直接从PCR扩增条带中进行测序。这些序列代表27个已知基因和37个新基因。通过Northern印迹分析,我们证实了总共23个基因(12个已知,11个新基因)的差异表达,而19个(7个已知,12个新基因)未显示差异表达。其他研究人员之前也曾观察到其中一些已知基因在年轻和衰老的成纤维细胞之间存在差异表达,从而验证了该技术。