Ardley H C, Moynihan T P, Thompson J, Leek J P, Markham A F, Robinson P A
Molecular Medicine Unit, St. James's University Hospital, Leeds, UK.
Cytogenet Cell Genet. 1997;79(3-4):188-92. doi: 10.1159/000134717.
We describe a rapid, PCR-based, screening procedure for the isolation of human genomic clones in lambda bacteriophage, containing sequences coding for individual homologous members of a multigene family. The approach is based upon the identification, by dilution, of sub-pools of the genomic library that contain members of the gene family, prior to phage isolation. The presence of specific genes is established by PCR of aliquots of individually amplified library pools, using consensus primers and subsequent sequencing. We have used the approach to isolate a fourth member of the UBE2L gene family, UBE2L4, and located it on chromosome 19q13.1-->q13.2. This PCR-based approach to library screening has wider applicability in that it could be used to isolate alternate-spliced products from cDNA libraries.
我们描述了一种基于聚合酶链反应(PCR)的快速筛选程序,用于从λ噬菌体中分离人基因组克隆,这些克隆包含编码多基因家族单个同源成员的序列。该方法基于在噬菌体分离之前,通过稀释鉴定基因组文库中包含基因家族成员的亚库。通过使用共有引物对单独扩增的文库池的等分试样进行PCR并随后测序,来确定特定基因的存在。我们已使用该方法分离出UBE2L基因家族的第四个成员UBE2L4,并将其定位在19号染色体的13.1→13.2区域。这种基于PCR的文库筛选方法具有更广泛的适用性,因为它可用于从cDNA文库中分离可变剪接产物。