Rickers A, Rininsland F, Osborne L, Reiss J
Institut für Humangenetik der Universität, Göttingen, Germany.
Hum Genet. 1994 Sep;94(3):311-3. doi: 10.1007/BF00208291.
The omission of complete exons in a proportion of mature transcripts has been shown for a variety of genes. In the case of the cystic fibrosis transmembrane conductance regulator gene, this phenomenon has previously been observed for exons 4, 9 and 12. Here, we describe the detection of a combined skipping of exons 11 and 12 in the absence of detectable transcripts missing only exon 11. This constellation has been found both in peripheral blood cells and in specifically expressing lung tissue, and excludes the possibility that the simultaneous skipping of both exons is merely a stochastic combination of single exon skipping events.
在多种基因的一部分成熟转录本中,已发现存在完全外显子缺失的情况。就囊性纤维化跨膜传导调节因子基因而言,此前已在外显子4、9和12中观察到这种现象。在此,我们描述了在未检测到仅缺失外显子11的转录本的情况下,外显子11和12联合跳跃的检测情况。这种情况在外周血细胞和特异性表达的肺组织中均已发现,并且排除了两个外显子同时跳跃仅仅是单个外显子跳跃事件的随机组合的可能性。