Ge H, Manley J L
Department of Biological Sciences, Columbia University, New York, New York 10027.
Cell. 1990 Jul 13;62(1):25-34. doi: 10.1016/0092-8674(90)90236-8.
SV40 early pre-mRNA is alternatively spliced by utilization of two different 5' splice sites and a shared 3' splice site to produce large T and small t mRNAs. The ratio of small t to large T mRNAs produced in human embryonic kidney 293 cells is 10- to 20-fold greater than in other mammalian cells, suggesting the existence of a 293 cell-specific factor that modulates alternative splicing. Here we show that nuclear extracts from 293 cells give rise to significantly more small t splicing than do extracts from HeLa cells. Using an in vitro complementation assay, we have characterized and extensively purified a factor from 293 extracts that brings about striking increases in small t splicing with concomitant decreases in large T splicing. The factor is heat sensitive and micrococcal nuclease resistant, suggesting that it is a protein lacking an accessible RNA component. Purification of the alternative splicing factor indicates that the activity is contained in one of several possibly related polypeptides of 30-35 kd.
SV40早期前体mRNA通过利用两个不同的5'剪接位点和一个共享的3'剪接位点进行可变剪接,以产生大T和小t mRNA。在人胚肾293细胞中产生的小t与大T mRNA的比例比其他哺乳动物细胞高10至20倍,这表明存在一种调节可变剪接的293细胞特异性因子。在这里,我们表明293细胞核提取物比HeLa细胞核提取物产生的小t剪接明显更多。使用体外互补试验,我们从293提取物中鉴定并广泛纯化了一种因子,该因子导致小t剪接显著增加,同时大T剪接减少。该因子对热敏感且抗微球菌核酸酶,表明它是一种缺乏可及RNA成分的蛋白质。可变剪接因子的纯化表明,活性存在于几种可能相关的30 - 35 kd多肽之一中。