Simoens C R, Peleman J, Valvekens D, Van Montagu M, Inzé D
Laboratorium voor Genetica, Rijksuniversiteit Gent, Belgium.
Gene. 1988 Jul 15;67(1):1-11. doi: 10.1016/0378-1119(88)90002-9.
The small genome size of Arabidopsis thaliana allows the isolation of genes expressed in specific tissues and under controlled conditions by the differential screening of a genomic library, as has been shown previously for yeast and Drosophila. cDNA probes, based on poly(A)+ mRNA isolated from different Arabidopsis organs, were used in colony hybridizations with 1145 randomly chosen genomic clones, representing 27,000 kb of Arabidopsis DNA. Twenty percent of the clones containing low-copy-number sequences hybridized with one or more of the cDNA probes that were synthesized from mRNA isolated from leaves, stems, seed pods, inflorescences, callus tissue, and light-grown and dark-grown plants. Comparison of the colony hybridizations led to the identification of a large variety of clones which contain differentially expressed genes. The pattern of expression was confirmed by Northern analysis. The advantage of the described method is that it yields directly genomic sequences that contain specifically expressed or induced genes. In particular, it circumvents the construction and differential screening of cDNA libraries for every tissue or environmental parameter to be analyzed.
拟南芥的小基因组使得通过对基因组文库进行差异筛选来分离在特定组织和受控条件下表达的基因成为可能,正如之前在酵母和果蝇中所展示的那样。基于从不同拟南芥器官中分离出的聚腺苷酸加尾(poly(A)+)信使核糖核酸(mRNA)制备的互补脱氧核糖核酸(cDNA)探针,被用于与1145个随机选择的基因组克隆进行菌落杂交,这些克隆代表了27000千碱基对(kb)的拟南芥DNA。20%含有低拷贝数序列的克隆与从叶片、茎、豆荚、花序、愈伤组织以及光照生长和黑暗生长的植物中分离的mRNA合成的一种或多种cDNA探针发生杂交。菌落杂交结果的比较导致鉴定出大量含有差异表达基因的克隆。通过Northern分析证实了表达模式。所描述方法的优点在于它直接产生包含特异性表达或诱导基因的基因组序列。特别是,它避免了针对每个要分析的组织或环境参数构建和差异筛选cDNA文库。