Lack of shielding of primer binding site silencer-mediated repression of an internal promoter in a retrovirus vector by the putative insulators scs, BEAD-1, and HS4

被引:16
作者
Modin, C
Pedersen, FS
Duch, M
机构
[1] Aarhus Univ, Dept Mol & Struct Biol, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ, Dept Med Microbiol & Immunol, DK-8000 Aarhus, Denmark
关键词
D O I
10.1128/JVI.74.24.11697-11707.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A major determinant for transcriptional incompetence of murine leukemia virus (MLV) and MLV-derived vectors in embryonal cells is located at the proline primer binding site (PBS). The mechanism of silencing is unknown, yet the effect is capable of spreading to adjacent promoters. Based on a retroviral vector containing an internal promoter and the escape mutant B2 PBS with expressional capacity in embryonal cells, we have developed an assay to test the ability of putative insulators to shield the silencer at the PBS. Since the B2 PBS reverts to the wild-type PBS at high frequency, a shielding ability of a putative insulator can be assessed from the ratio of expressing B2 PBS to proline PBS proviruses in the target embryonal carcinoma cell population as measured by primer extension. Our results show that none of the possible insulators, scs, BEAD-1, or HS4, is able to shield an internal promoter from the repressive effect of the silencer at the PBS region when inserted between the silencer and the promoter.
引用
收藏
页码:11697 / 11707
页数:11
相关论文
共 79 条
[31]   A GROUP OF SCS ELEMENTS FUNCTION AS DOMAIN BOUNDARIES IN AN ENHANCER-BLOCKING ASSAY [J].
KELLUM, R ;
SCHEDL, P .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (05) :2424-2431
[32]   CHARACTERIZATION OF THE MOLONEY MURINE LEUKEMIA-VIRUS STEM CELL-SPECIFIC REPRESSOR BINDING-SITE [J].
KEMPLER, G ;
FREITAG, B ;
BERWIN, B ;
NANASSY, O ;
BARKLIS, E .
VIROLOGY, 1993, 193 (02) :690-699
[33]   NEP1 - A UBIQUITOUS TRANSCRIPTION FACTOR SYNERGIZES WITH V-ERBA IN TRANSCRIPTIONAL SILENCING [J].
KOHNE, AC ;
BANIAHMAD, A ;
RENKAWITZ, R .
JOURNAL OF MOLECULAR BIOLOGY, 1993, 232 (03) :747-755
[34]   Host cis-mediated extinction of a retrovirus permissive for expression in embryonal stem cells during differentiation [J].
Laker, C ;
Meyer, J ;
Schopen, A ;
Friel, J ;
Heberlein, C ;
Ostertag, W ;
Stocking, C .
JOURNAL OF VIROLOGY, 1998, 72 (01) :339-348
[35]   RETROVIRAL VECTOR GENE-EXPRESSION IN F9 EMBRYONAL CARCINOMA-CELLS [J].
LINNEY, E ;
NEILL, SD ;
PRESTRIDGE, DS .
JOURNAL OF VIROLOGY, 1987, 61 (10) :3248-3253
[36]   NON-FUNCTION OF A MOLONEY MURINE LEUKEMIA-VIRUS REGULATORY SEQUENCE IN F9 EMBRYONAL CARCINOMA-CELLS [J].
LINNEY, E ;
DAVIS, B ;
OVERHAUSER, J ;
CHAO, E ;
FAN, H .
NATURE, 1984, 308 (5958) :470-472
[37]   NEGATIVE REGULATION OF RETROVIRUS EXPRESSION IN EMBRYONAL CARCINOMA-CELLS MEDIATED BY AN INTRAGENIC DOMAIN [J].
LOH, TP ;
SIEVERT, LL ;
SCOTT, RW .
JOURNAL OF VIROLOGY, 1988, 62 (11) :4086-4095
[38]   EVIDENCE FOR A STEM CELL-SPECIFIC REPRESSOR OF MOLONEY MURINE LEUKEMIA-VIRUS EXPRESSION IN EMBRYONAL CARCINOMA-CELLS [J].
LOH, TP ;
SIEVERT, LL ;
SCOTT, RW .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (08) :4045-4057
[39]   PROVIRAL SEQUENCES THAT RESTRICT RETROVIRAL EXPRESSION IN MOUSE EMBRYONAL CARCINOMA-CELLS [J].
LOH, TP ;
SIEVERT, LL ;
SCOTT, RW .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (10) :3775-3784
[40]   MUTATED PRIMER BINDING SITES INTERACTING WITH DIFFERENT TRNAS ALLOW EFFICIENT MURINE LEUKEMIA VIRUS REPLICATION [J].
LUND, AH ;
DUCH, M ;
LOVMAND, J ;
JORGENSEN, P ;
PEDERSEN, FS .
JOURNAL OF VIROLOGY, 1993, 67 (12) :7125-7130