Novel retroviral vectors to facilitate expression screens in mammalian cells.

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.

[1]  R. Bernards,et al.  A System for Stable Expression of Short Interfering RNAs in Mammalian Cells , 2002, Science.

[2]  René Bernards,et al.  A senescence rescue screen identifies BCL6 as an inhibitor of anti-proliferative p19(ARF)-p53 signaling. , 2002, Genes & development.

[3]  G. Daley,et al.  A functional screen identifies hDRIL1 as an oncogene that rescues RAS-induced senescence , 2002, Nature Cell Biology.

[4]  Marc J. van de Vijver,et al.  Senescence bypass screen identifies TBX2, which represses Cdkn2a (p19ARF) and is amplified in a subset of human breast cancers , 2000, Nature Genetics.

[5]  A. Miyajima,et al.  Constitutive Activation of STAT5 by a Point Mutation in the SH2 Domain* , 2000, The Journal of Biological Chemistry.

[6]  R. Jaenisch,et al.  V(D)J recombination is not activated by demethylation of the kappa locus. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[7]  G. Daley,et al.  A genetic screen to identify genes that rescue the slow growth phenotype of c-myc null fibroblasts , 2000, Oncogene.

[8]  G. Hannon,et al.  MaRX: An Approach to Genetics in Mammalian Cells , 1999, Science.

[9]  A. Kimchi,et al.  Death associated proteins (DAPs): from gene identification to the analysis of their apoptotic and tumor suppressive functions , 1998, Oncogene.

[10]  L. Lau,et al.  Isolation of growth suppressors from a cDNA expression library , 1998, Oncogene.

[11]  M. McMahon,et al.  Identification and Characterization of a Constitutively Active STAT5 Mutant That Promotes Cell Proliferation , 2022 .

[12]  A. Kimchi,et al.  Death-associated proteins: from gene identification to the analysis of their apoptotic and tumour suppressive functions. , 1998, Molecular medicine today.

[13]  G. Daley,et al.  Secondary mutation maintains the transformed state in BaF3 cells with inducible BCR/ABL expression. , 1998, Blood.

[14]  A. Kimchi DAP genes: novel apoptotic genes isolated by a functional approach to gene cloning. , 1998, Biochimica et Biophysica Acta.

[15]  D. Littman,et al.  Expression cloning of new receptors used by simian and human immunodeficiency viruses , 1997, Nature.

[16]  Warren S. Alexander,et al.  A family of cytokine-inducible inhibitors of signalling , 1997, Nature.

[17]  G. Nolan,et al.  Identification of an oncogenic form of the thrombopoietin receptor MPL using retrovirus-mediated gene transfer. , 1996, Blood.

[18]  R. Naviaux,et al.  The pCL vector system: rapid production of helper-free, high-titer, recombinant retroviruses , 1996, Journal of virology.

[19]  G. Nolan,et al.  Applications of retrovirus-mediated expression cloning. , 1996, Experimental hematology.

[20]  A. Kimchi,et al.  Isolation of DAP3, a Novel Mediator of Interferon-γ-induced Cell Death (*) , 1995, The Journal of Biological Chemistry.

[21]  G. Nolan,et al.  Efficient screening of retroviral cDNA expression libraries. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[22]  Robert Kay,et al.  Expression cloning of oncogenes by retroviral transfer of cDNA libraries , 1995, Molecular and cellular biology.

[23]  J. Bergemann,et al.  Excision of specific DNA-sequences from integrated retroviral vectors via site-specific recombination. , 1995, Nucleic acids research.

[24]  L. Lau,et al.  Genetic selection of growth-inhibitory sequences in mammalian cells. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[25]  H. Chen,et al.  High-efficiency identification of genes by functional analysis from a retroviral cDNA expression library , 1994, Journal of Virology.

[26]  I. Mazo,et al.  Cloning mammalian genes by expression selection of genetic suppressor elements: association of kinesin with drug resistance and cell immortalization. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[27]  J. Rayner,et al.  A simple and efficient procedure for generating stable expression libraries by cDNA cloning in a retroviral vector. , 1994, Molecular and cellular biology.

[28]  E. Jaffee,et al.  Vaccination with irradiated tumor cells engineered to secrete murine granulocyte-macrophage colony-stimulating factor stimulates potent, specific, and long-lasting anti-tumor immunity. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[29]  G. Nolan,et al.  Production of high-titer helper-free retroviruses by transient transfection. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[30]  R. Legerski,et al.  High-frequency transformation of human repair-deficient cell lines by an Epstein-Barr virus-based cDNA expression vector. , 1991, Gene.

[31]  A. Kimchi,et al.  A genetic tool used to identify thioredoxin as a mediator of a growth inhibitory signal. , 1991, Science.

[32]  David Baltimore,et al.  The V(D)J recombination activating gene, RAG-1 , 1989, Cell.

[33]  P. Palese,et al.  Expression of antisense RNA fails to inhibit influenza virus replication , 1989, Virus Research.

[34]  G. Stark,et al.  Excess antisense RNA from infectious recombinant SV40 fails to inhibit expression of a transfected, interferon-inducible gene. , 1988, European journal of biochemistry.

[35]  A. Gatignol,et al.  Bleomycin resistance conferred by a drug‐binding protein , 1988, FEBS letters.

[36]  B. Seed,et al.  Molecular cloning of a CD28 cDNA by a high-efficiency COS cell expression system. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[37]  M. Bender,et al.  Evidence that the packaging signal of Moloney murine leukemia virus extends into the gag region , 1987, Journal of virology.

[38]  R. Jaenisch,et al.  Replication-competent Moloney murine leukemia virus carrying a bacterial suppressor tRNA gene: selective cloning of proviral and flanking host sequences. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[39]  E. Chang,et al.  Pathogenicity of retroviruses containing either the normal human c-Ha-ras1 gene or its mutated form derived from the bladder carcinoma EJ/T24 cell line. , 1985, Journal of experimental pathology.

[40]  C. Cepko,et al.  Construction and applications of a highly transmissible murine retrovirus shuttle vector , 1984, Cell.

[41]  R. Weinberg,et al.  Isolation of a transforming sequence from a human bladder carcinoma cell line , 1982, Cell.

[42]  M. Wigler,et al.  Isolation and preliminary characterization of a human transforming gene from T24 bladder carcinoma cells , 1982, Nature.