Moussa N M, Lobo S M, Marzluff W F
Gene. 1985;36(3):311-9. doi: 10.1016/0378-1119(85)90186-6.
A 6.9-kb DNA fragment containing two mouse U1b genes was introduced by cotransfection with the Herpes simplex virus (HSV) thymidine kinase (TK) gene into tk- mouse L cells. The parent Ltk- cells produce primarily U1a RNA and only small amounts of U1b RNA. However, after introduction of exogenous U1b genes by cotransfection these cells express large amounts of U1b RNA. Subcloned DNA fragments containing a single U1b gene and varying amounts of DNA flanking the 5' -end of the gene were introduced into Ltk- cells. All of the constructs containing 400 bp or more upstream of the U1b gene were efficiently expressed. By comparison, a subclone containing only 150 bp of DNA flanking the 5' -end of the U1b gene was not efficiently expressed. The U1b transcripts synthesized in transfected cells were identified by hybrid selection and by precipitation of ribonucleoproteins (RNP) containing U1 RNA with anti-RNP antibody.
一个包含两个小鼠U1b基因的6.9千碱基对DNA片段与单纯疱疹病毒(HSV)胸苷激酶(TK)基因共转染到tk -小鼠L细胞中。亲代Ltk -细胞主要产生U1a RNA,仅产生少量U1b RNA。然而,通过共转染引入外源U1b基因后,这些细胞大量表达U1b RNA。将含有单个U1b基因以及该基因5'端侧翼不同长度DNA的亚克隆DNA片段引入Ltk -细胞。所有含有U1b基因上游400碱基对或更多碱基对的构建体都能高效表达。相比之下,一个仅含有U1b基因5'端侧翼150碱基对DNA的亚克隆则不能高效表达。通过杂交筛选以及用抗核糖核蛋白(RNP)抗体沉淀含有U1 RNA的核糖核蛋白(RNP),鉴定了转染细胞中合成的U1b转录本。