Koh Eugene Y, Chen Tong, Daley George Q
Whitehead Institute, Nine Cambridge Center, Cambridge, MA 02142, USA.
Nucleic Acids Res. 2002 Dec 15;30(24):e142. doi: 10.1093/nar/gnf142.
As tools for functional genomics, expression profiling and proteomics provide correlative data, while expression cloning screens can link genes directly to biological function. However, technical limitations of gene transfer, expression, and recovery of candidate genes have limited wider application of genome-wide expression screens. Here we describe the pEYK retroviral vectors, which maintain high titers and robust gene expression while addressing the major bottleneck of expression cloning--efficient candidate gene recovery. By exploiting schemes for enhanced PCR rescue or strategies for direct isolation of proviral DNA as plasmids in bacterial hosts, the pEYK vectors facilitate cDNA isolation from selected cells and enable rapid iteration of screens and genetic reversion analyses to validate gene candidates. These vectors have proven useful to identify genes linked to cell proliferation, senescence and apoptosis.
作为功能基因组学的工具,表达谱分析和蛋白质组学提供相关数据,而表达克隆筛选可将基因直接与生物学功能联系起来。然而,基因转移、表达及候选基因回收的技术局限性限制了全基因组表达筛选的更广泛应用。在此,我们描述了pEYK逆转录病毒载体,其在解决表达克隆的主要瓶颈——高效回收候选基因的同时,保持高滴度和强劲的基因表达。通过采用增强型PCR拯救方案或在细菌宿主中作为质粒直接分离前病毒DNA的策略,pEYK载体便于从选定细胞中分离cDNA,并能快速进行筛选迭代和基因回复分析以验证候选基因。这些载体已被证明可用于鉴定与细胞增殖、衰老和凋亡相关的基因。