Kato K
Okayama Cell Switching Project, ERATO, JRDC, Kyoto, Japan.
Nucleic Acids Res. 1995 Sep 25;23(18):3685-90. doi: 10.1093/nar/23.18.3685.
A novel means of recording the expression status of the total gene population is described. Digestion of cDNA by class IIS restriction enzymes produces a fragment with a poly (A) stretch and a 5' overhang with an unknown sequence. This fragment contains information such as the class IIS enzyme that cuts cDNA nearest to the poly (A) stretch, the sequence of the 5' overhang, and the size of the fragment. Expressed genes can be discriminated and displayed by the fragment as follows: (i) cut the cDNA with one class IIS restriction enzyme; (ii) ligate the digested cDNA to that from a pool of 64 biotinylated adaptors cohesive to all possible overhangs; (iii) digest by other two class IIS enzymes; (iv) recover the ligated molecules with streptavidin-coated paramagnetic beads; (v) perform PCR with the adaptor-primer and an anchored oligo-dT primer; (vi) separate the amplified fragments by denaturing polyacrylamide gel electrophoresis. Repeat the experiment with 64 adaptors, three enzymes and three anchored oligo-dT primers displays most of the expressed genes. Because redundancy is minimized, this technique is also ideal for generating tags for expressed genes, with which to construct a transcript map of the genome.
本文描述了一种记录全基因组表达状态的新方法。用II类限制性内切酶消化cDNA会产生一个带有poly(A)尾和未知序列5'突出端的片段。该片段包含诸如最靠近poly(A)尾切割cDNA的II类酶、5'突出端的序列以及片段大小等信息。表达的基因可通过该片段按以下方式进行区分和展示:(i) 用一种II类限制性内切酶切割cDNA;(ii) 将消化后的cDNA与64种生物素化接头的混合物连接,这些接头与所有可能的突出端互补;(iii) 用另外两种II类酶消化;(iv) 用链霉亲和素包被的顺磁珠回收连接的分子;(v) 用接头引物和锚定寡聚dT引物进行PCR;(vi) 通过变性聚丙烯酰胺凝胶电泳分离扩增片段。用64种接头、三种酶和三种锚定寡聚dT引物重复该实验可展示大多数表达的基因。由于冗余度最小化,该技术也是生成表达基因标签以构建基因组转录图谱的理想方法。