Lapoumeroulie C, Acuto S, Rouabhi F, Labie D, Krishnamoorthy R, Bank A
Institut National de la Sante et de la Recherche Medicale, Faculte de Medecine Cochin Port-Royal, Paris, France.
Nucleic Acids Res. 1987 Oct 26;15(20):8195-204. doi: 10.1093/nar/15.20.8195.
Expression of a cloned human beta thalassemia gene with a single base change at position 5 of IVS 1 has been analyzed 48 hours after transfer of the gene into HeLa cells (transient expression). Little or no normal beta globin mRNA accumulates in the presence of the abnormal beta gene in contrast to significantly more normal beta mRNA produced with other mutations at this same position. By contrast, large amounts of an abnormal beta globin mRNA are present; this is due to the use of a cryptic 5' splice site in exon 1 rather than the normal 5' splice site of IVS 1. The results indicate the variability of the effect on RNA splicing of different single base defects within IVS.
在将该基因导入HeLa细胞48小时后(瞬时表达),对一个在IVS 1第5位有单个碱基变化的克隆人β地中海贫血基因的表达进行了分析。与在同一位置的其他突变产生的正常β mRNA明显增多形成对比的是,在异常β基因存在的情况下,几乎没有正常β珠蛋白mRNA积累。相比之下,存在大量异常β珠蛋白mRNA;这是由于外显子1中一个隐蔽的5'剪接位点被使用,而不是IVS 1的正常5'剪接位点。结果表明IVS内不同单碱基缺陷对RNA剪接的影响具有变异性。