Zelenin S M, Popova V S, Morozov I V, Tishkov V I, Egorov A M, Mertvetsov N P
Bioorg Khim. 1991 Jul;17(7):994-6.
EcoRI-fragment No. 5 of the rat tyrosine aminotransferase gene containing exons K, L, intron 11, and a part of the 3'-nontranslatable region was digested with several restriction endonucleases (BspRI, Sau3A, BamHI, Ecl136II, AluI), the subfragments obtained were cloned into M13mp19 and sequenced using the Sanger technique with dye-labelled primers on the automated sequencer "Applied Biosystems", model 370A. The sequences were combined by means of a PC-GENE package and original programs to yield the primary structure (1064 b. p.) of the above fragment No. 5, adjacent to the previously sequenced EcoRI-fragment No. 4 (3677 b.p.).
大鼠酪氨酸转氨酶基因的EcoRI片段5包含外显子K、L、内含子11和部分3'-非翻译区,用几种限制性内切酶(BspRI、Sau3A、BamHI、Ecl136II、AluI)进行消化,得到的亚片段克隆到M13mp19中,并在“Applied Biosystems”370A型自动测序仪上使用带染料标记引物的桑格技术进行测序。通过PC-GENE软件包和原始程序将序列组合起来,得到上述片段5(1064个碱基对)的一级结构,该片段与先前测序的EcoRI片段4(3677个碱基对)相邻。