Gulick P J, Dvorák J
Department of Agronomy and Range Science, University of California, Davis 95616.
Gene. 1990 Nov 15;95(2):173-7. doi: 10.1016/0378-1119(90)90359-y.
We present a novel technique for the enrichment of cDNA libraries to enhance the abundance of clones of differentially expressed genes. The technique is relatively simple, requires moderate quantities of poly(A) + RNA and results in preferential enrichment of clones derived from mRNAs that were of low abundance in their original population. This method was used to isolate cDNA clones of salt-stress-induced genes in the roots of Lophopyrum elongatum, a highly salt-tolerant wheatgrass. An excess of sonicated plasmid DNA from a cDNA library from nonstressed roots was hybridized in a formamide-phenol emulsion with inserts from a cDNA library of stressed roots. Clones that were more abundant in, or were unique to, the library of the stressed roots were recovered as double-stranded fragments by virtue of reconstituted restriction-enzyme-digested ends by ligating them to a plasmid vector. The resulting enriched library was screened by differential colony hybridization and clones of eleven different genes that were more strongly expressed in stressed roots than in controls were selected.
我们提出了一种用于富集cDNA文库以提高差异表达基因克隆丰度的新技术。该技术相对简单,需要适量的聚腺苷酸加尾RNA,并能优先富集源自其原始群体中低丰度mRNA的克隆。此方法用于分离长穗偃麦草(一种高度耐盐的小麦草)根部盐胁迫诱导基因的cDNA克隆。来自未受胁迫根部的cDNA文库中过量的超声处理质粒DNA与受胁迫根部的cDNA文库中的插入片段在甲酰胺 - 苯酚乳液中杂交。通过将它们连接到质粒载体上,借助重组的限制性内切酶消化末端,将在受胁迫根部文库中丰度更高或特有的克隆回收为双链片段。通过差异菌落杂交筛选所得的富集文库,并选择了11个在受胁迫根部比对照中表达更强的不同基因的克隆。