THE PROKARYOTIC NEOMYCIN-RESISTANCE-ENCODING GENE ACTS AS A TRANSCRIPTIONAL SILENCER IN EUKARYOTIC CELLS

被引:120
作者
ARTELT, P
GRANNEMANN, R
STOCKING, C
FRIEL, J
BARTSCH, J
HAUSER, H
机构
[1] GESELL BIOTECHNOL FORSCH GMBH,CELL BIOL & GENET SECT,MASCHERODER WEG 1,W-3300 BRAUNSCHWEIG,GERMANY
[2] UNIV HAMBURG,HEINRICH PETTE INST EXPTL VIROL & IMMUNOL,W-2000 HAMBURG 20,GERMANY
关键词
RETROVIRAL VECTORS; RECOMBINANT DNA; NEOMYCIN PHOSPHOTRANSFERASE; TRANSCRIPTIONAL INTERFERENCE; EXPRESSION VECTORS;
D O I
10.1016/0378-1119(91)90134-W
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The gene encoding neomycin resistance (neo) mediates a cis-acting negative effect on expression from promoters in transient and stable transfectants of mammalian cell lines. Inserting the neo gene either into retroviral vectors or into plasmids containing reporter genes results in a five- to tenfold decrease of expression from proximal promoters like the simian virus 40 early or the retroviral myeloproliferative sarcoma virus promoter. The silencing effect is not dependent on the insertion site or the orientation of the fragment. The neo gene is frequently used in eukaryotic vectors as a dominant selectable gene. Other selectable genes were tested for potential cis-activity. We found that the gene conferring resistance to puromycin from Streptomyces alboniger does not influence adjacent promoters.
引用
收藏
页码:249 / 254
页数:6
相关论文
共 22 条
[11]   RECOMBINANT GENOMES WHICH EXPRESS CHLORAMPHENICOL ACETYLTRANSFERASE IN MAMMALIAN-CELLS [J].
GORMAN, CM ;
MOFFAT, LF ;
HOWARD, BH .
MOLECULAR AND CELLULAR BIOLOGY, 1982, 2 (09) :1044-1051
[12]   NEW TECHNIQUE FOR ASSAY OF INFECTIVITY OF HUMAN ADENOVIRUS 5 DNA [J].
GRAHAM, FL ;
VANDEREB, AJ .
VIROLOGY, 1973, 52 (02) :456-467
[13]   MOLECULAR-CLONING AND CHARACTERIZATION OF A HUMAN DNA-BINDING FACTOR THAT REPRESSES TRANSCRIPTION [J].
KAGEYAMA, R ;
PASTAN, I .
CELL, 1989, 59 (05) :815-825
[14]   MOLECULAR-CLONING AND CHARACTERIZATION OF A LEUKEMIA-INDUCING MYELOPROLIFERATIVE SARCOMA-VIRUS AND 2 OF ITS TEMPERATURE-SENSITIVE MUTANTS [J].
KOLLEK, R ;
STOCKING, C ;
SMADJAJOFFE, F ;
OSTERTAG, W .
JOURNAL OF VIROLOGY, 1984, 50 (03) :717-724
[15]   AUTOCRINE STIMULATION AFTER TRANSFER OF THE GRANULOCYTE MACROPHAGE COLONY-STIMULATING FACTOR GENE AND AUTONOMOUS GROWTH ARE DISTINCT BUT INTERDEPENDENT STEPS IN THE ONCOGENIC PATHWAY [J].
LAKER, C ;
STOCKING, C ;
BERGHOLZ, U ;
HESS, N ;
DELAMARTER, JF ;
OSTERTAG, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (23) :8458-8462
[16]   SELECTION FOR ANIMAL-CELLS THAT EXPRESS THE ESCHERICHIA-COLI GENE CODING FOR XANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE [J].
MULLIGAN, RC ;
BERG, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (04) :2072-2076
[17]   THE MYELOPROLIFERATIVE SARCOMA-VIRUS RETAINS TRANSFORMING FUNCTIONS AFTER INTRODUCTION OF A DOMINANT SELECTABLE MARKER GENE [J].
OSTERTAG, W ;
SELIGER, B ;
KOLLEK, R ;
STOCKING, C ;
BERGHOLZ, U ;
SMADJAJOFFE, F .
JOURNAL OF GENERAL VIROLOGY, 1986, 67 :1361-1371
[18]  
Sambrook J., 1989, MOL CLONING LAB MANU
[19]   LONG TERMINAL REPEAT SEQUENCES IMPART HEMATOPOIETIC TRANSFORMATION PROPERTIES TO THE MYELOPROLIFERATIVE SARCOMA-VIRUS [J].
STOCKING, C ;
KOLLEK, R ;
BERGHOLZ, U ;
OSTERTAG, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (17) :5746-5750
[20]   STRUCTURE AND EXPRESSION OF A CLONED CDNA FOR HUMAN INTERLEUKIN-2 [J].
TANIGUCHI, T ;
MATSUI, H ;
FUJITA, T ;
TAKAOKA, C ;
KASHIMA, N ;
YOSHIMOTO, R ;
HAMURO, J .
NATURE, 1983, 302 (5906) :305-310