Mulder L C, Rossini M, Mora M
IRIS, The Chiron Biocine Immunobiological Research Institute, Siena, Italy.
Gene. 1997 Feb 20;186(1):83-6. doi: 10.1016/s0378-1119(96)00685-3.
RNA analysis of mice transgenic for human CD46 reveals almost undetectable levels of the expected transcript and the accumulation of a 900 nt shorter species. cDNA cloning and sequence analysis of this variant demonstrate an aberrant splicing of the transgene RNA. This aberrant splicing is present at low levels in cells that normally express the gene, suggesting that the transgene is lacking regulatory elements influencing the abundance of the shorter transcript.
对转人CD46基因小鼠的RNA分析显示,预期转录本水平几乎检测不到,且积累了一种短900个核苷酸的物种。对该变体进行cDNA克隆和序列分析表明转基因RNA存在异常剪接。这种异常剪接在正常表达该基因的细胞中水平较低,这表明转基因缺乏影响较短转录本丰度的调控元件。