Rambosek J A, Kinsey J A
Gene. 1984 Jan;27(1):101-7. doi: 10.1016/0378-1119(84)90242-7.
We have cloned the unstable am mutant gene, am126, as well as the am gene from an am126 revertant. The mutation is a result of a 33-bp duplication that repeats a sequence starting 13 bp upstream of the 3' splice junction between intron 1 and exon 2 and extends 20 bp into exon 2. In addition, there is a G----A transition 2 bp upstream of the first copy of the duplicated sequence. In the revertant gene the wild-type sequence is precisely recovered, involving both the loss of the duplication and a reversion (A----G) of the associated transition. Our data suggest that only the more 5' of the two 3' splice junctions present in the duplicated version of the gene is used. This favors a 5'----3' scanning mechanism for exon splicing.
我们已经克隆了不稳定的am突变基因am126,以及来自am126回复体的am基因。该突变是由于33bp的重复造成的,该重复重复了一个序列,该序列从内含子1和外显子2之间3'剪接位点上游13bp处开始,并延伸到外显子2中20bp处。此外,在重复序列的第一个拷贝上游2bp处有一个G→A转换。在回复体基因中,野生型序列被精确恢复,包括重复序列的丢失和相关转换的回复(A→G)。我们的数据表明,基因重复版本中存在的两个3'剪接位点中只有更靠近5'端的那个被使用。这有利于外显子剪接的5'→3'扫描机制。