Generation of RCAS vectors useful for functional genomic analyses

被引:50
作者
Loftus, SK
Larson, DM
Watkins-Chow, D
Church, DM
Pavan, WJ
机构
[1] NHGRI, Mouse Embryol Sect, Genet Dis Res Inst, NIH, Bethesda, MD 20892 USA
[2] NIH, Natl Ctr Biotechnol Informat, Bethesda, MD 20892 USA
关键词
RCAS; tv-a; retrovirus; recombination; Gateway; gene expression;
D O I
10.1093/dnares/8.5.221
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Avian leukosis type A virus-derived retroviral vectors have been used to introduce genes into cells expressing the corresponding avian receptor tv-a. This includes the use of Replication-Competent Avian sarcoma-leukosis virus (ASLV) long terminal repeat (LTR) with Splice acceptor (RCAS) vectors in the analysis of avian development, human and murine cell cultures, murine cell lineage studies and cancer biology. Previously, cloning of genes into this virus was difficult due to the large size of the vector and sparse cloning sites. To overcome some of the disadvantages of traditional cloning using the RCASBP-Y vector, we have modified the RCASBP-Y to incorporate "Gateway" site-specific recombination cloning of genes into the construct, either with or without HA epitope tags. We have found the repetitive "att" sequences, which are the targets for site-specific recombination, do not impair the production of infectious viral particles or the expression of the gene of interest. This is the first instance of site-specific recombination being used to generate retroviral gene constructs. These viral constructs will allow for the efficient transfer and expression of cDNAs needed for functional genomic analyses.
引用
收藏
页码:221 / 226
页数:6
相关论文
共 23 条
  • [1] Genetic mapping of the cloned subgroup A avian sarcoma and leukosis virus receptor gene to the TVA locus
    Bates, P
    Rong, LJ
    Varmus, HE
    Young, JAT
    Crittenden, LB
    [J]. JOURNAL OF VIROLOGY, 1998, 72 (03) : 2505 - 2508
  • [2] A RECEPTOR FOR SUBGROUP-A ROUS-SARCOMA VIRUS IS RELATED TO THE LOW-DENSITY-LIPOPROTEIN RECEPTOR
    BATES, P
    YOUNG, JAT
    VARMUS, HE
    [J]. CELL, 1993, 74 (06) : 1043 - 1051
  • [3] A LINE OF NONTUMORIGENIC MOUSE MELANOCYTES, SYNGENEIC WITH THE B-16 MELANOMA AND REQUIRING A TUMOR PROMOTER FOR GROWTH
    BENNETT, DC
    COOPER, PJ
    HART, IR
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1987, 39 (03) : 414 - 418
  • [4] A NEW DEFECTIVE RETROVIRAL VECTOR SYSTEM BASED ON THE BRYAN STRAIN OF ROUS-SARCOMA VIRUS
    BOERKOEL, CF
    FEDERSPIEL, MJ
    SALTER, DW
    PAYNE, W
    CRITTENDEN, LB
    KUNG, HJ
    HUGHES, SH
    [J]. VIROLOGY, 1993, 195 (02) : 669 - 679
  • [5] CARNINCI P, 2001, IN PRESS GENOMICS
  • [6] Neural crest-directed gene transfer demonstrates Wnt1 role in melanocyte expansion and differentiation during mouse development
    Dunn, KJ
    Williams, BO
    Li, Y
    Pavan, WJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (18) : 10050 - 10055
  • [7] In utero complementation of a neural crest-derived melanocyte defect using cell directed gene transfer
    Dunn, KJ
    Incao, A
    Watkins-Chow, D
    Li, Y
    Pavan, WJ
    [J]. GENESIS, 2001, 30 (02) : 70 - 76
  • [8] Expression of transduced genes in mice generated by infecting blastocysts with avian leukosis virus-based retroviral vectors
    Federspiel, MJ
    Swing, DA
    Eagleson, B
    Reid, SW
    Hughes, SH
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (10) : 4931 - 4936
  • [9] A SYSTEM FOR TISSUE-SPECIFIC GENE TARGETING - TRANSGENIC MICE SUSCEPTIBLE TO SUBGROUP-A AVIAN-LEUKOSIS VIRUS-BASED RETROVIRAL VECTORS
    FEDERSPIEL, MJ
    BATES, P
    YOUNG, JAT
    VARMUS, HE
    HUGHES, SH
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (23) : 11241 - 11245
  • [10] Development of a flexible and specific gene delivery system for production of murine tumor models
    Fisher, GH
    Orsulic, S
    Holland, E
    Hively, WP
    Li, Y
    Lewis, BC
    Williams, BO
    Varmus, HE
    [J]. ONCOGENE, 1999, 18 (38) : 5253 - 5260