Novel retroviral vectors to facilitate expression screens in mammalian cells
Author(s) -
Eugene Y. Koh
Publication year - 2002
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gnf142
Subject(s) - biology , gene , computational biology , functional genomics , gene expression profiling , plasmid , expression cloning , genome , genetics , cloning (programming) , dna microarray , gene expression , complementary dna , genomics , computer science , programming language
As tools for functional genomics, expression profil- ing and proteomics provide correlative data, while expression cloning screens can link genes directly to biological function. However, technical limita- tions 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.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom