A NEGATIVE ELEMENT INVOLVED IN VIMENTIN GENE-EXPRESSION

被引:67
作者
FARRELL, FX
SAX, CM
ZEHNER, ZE
机构
[1] VIRGINIA COMMONWEALTH UNIV, MED COLL VIRGINIA, DEPT BIOCHEM & MOLEC BIOPHYS, RICHMOND, VA 23298 USA
[2] NEI, MOLEC & DEV BIOL LAB, BETHESDA, MD 20892 USA
[3] VIRGINIA COMMONWEALTH UNIV, MED COLL VIRGINIA, MASSEY CANC CTR, RICHMOND, VA 23298 USA
关键词
D O I
10.1128/MCB.10.5.2349
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vimentin is one member of the intermediate filament multigene family which exhibits both tissue- and developmental stage-specific expression. In vivo, vimentin is expressed in cells of mesenchymal origin. Previously, we identified both enhancer and promoter elements in the chicken vimentin gene which regulate gene expression in a positive manner. In this report, we have identified a 40-base-pair region at -568 base pairs between the proximal and distal enhancer elements which represses transcriptional activity. This silencer region can also repress the heterologous herpes simplex virus thymidine kinase promoter, which is comparable to the vimentin promoter. In addition, the element is able to function in a position- and orientation-independent manner, and the amount of repression is increased by multiple copies. Here we show by gel retardation assays and DNase I footprinting that this region binds a protein in nuclear extracts from HeLa cells. Southwestern (DNA-protein) blot analysis indicates this protein is approximately 95 kilodaltons in size. Moreover, protein distribution and activity mimic the expression pattern of vimentin during myogenesis, i.e., protein binding increases as vimentin gene expression decreases. The silencer region shares strong sequence similarity with 5'-flanking sequences found in both the human and hamster vimentin genes and with other characterized silencer elements, including the human immunodeficiency virus long terminal repeat, rat growth hormone, chicken lysozyme, and rat insulin genes. Thus, a negative element appears to bind a 95-kilodalton protein involved in regulating the tissue-specific expression of the chicken vimentin gene.
引用
收藏
页码:2349 / 2358
页数:10
相关论文
共 55 条
[1]   REGULATION OF THE LOW-DENSITY LIPOPROTEIN RECEPTOR AND HYDROXYMETHYLGLUTARYL COENZYME-A REDUCTASE GENES BY PROTEIN KINASE-C AND A PUTATIVE NEGATIVE REGULATORY PROTEIN [J].
AUWERX, JH ;
CHAIT, A ;
DEEB, SS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (04) :1133-1137
[2]   ACTIVITY OF 2 DIFFERENT SILENCER ELEMENTS OF THE CHICKEN LYSOZYME GENE CAN BE COMPENSATED BY ENHANCER ELEMENTS [J].
BANIAHMAD, A ;
MULLER, M ;
STEINER, C ;
RENKAWITZ, R .
EMBO JOURNAL, 1987, 6 (08) :2297-2303
[3]   OBP100 BINDS REMARKABLY DEGENERATE OCTAMER MOTIFS THROUGH SPECIFIC INTERACTIONS WITH FLANKING SEQUENCES [J].
BAUMRUKER, T ;
STURM, R ;
HERR, W .
GENES & DEVELOPMENT, 1988, 2 (11) :1400-1413
[4]   A PURIFIED DROSOPHILA HOMEODOMAIN PROTEIN REPRESSES TRANSCRIPTION INVITRO [J].
BIGGIN, MD ;
TJIAN, R .
CELL, 1989, 58 (03) :433-440
[5]   THE SAME INDUCIBLE NUCLEAR PROTEINS REGULATES MITOGEN ACTIVATION OF BOTH THE INTERLEUKIN-2 RECEPTOR-ALPHA GENE AND TYPE-1 HIV [J].
BOHNLEIN, E ;
LOWENTHAL, JW ;
SIEKEVITZ, M ;
BALLARD, DW ;
FRANZA, BR ;
GREENE, WC .
CELL, 1988, 53 (05) :827-836
[6]   PURIFICATION AND BIOCHEMICAL-CHARACTERIZATION OF THE PROMOTER-SPECIFIC TRANSCRIPTION FACTOR, SPL [J].
BRIGGS, MR ;
KADONAGA, JT ;
BELL, SP ;
TJIAN, R .
SCIENCE, 1986, 234 (4772) :47-52
[7]   PEMBL - A NEW FAMILY OF SINGLE STRANDED PLASMIDS [J].
DENTE, L ;
CESARENI, G ;
CORTESE, R .
NUCLEIC ACIDS RESEARCH, 1983, 11 (06) :1645-1655
[8]   ACCURATE TRANSCRIPTION INITIATION BY RNA POLYMERASE-II IN A SOLUBLE EXTRACT FROM ISOLATED MAMMALIAN NUCLEI [J].
DIGNAM, JD ;
LEBOVITZ, RM ;
ROEDER, RG .
NUCLEIC ACIDS RESEARCH, 1983, 11 (05) :1475-1489
[9]   CONTROL OF EUKARYOTIC MESSENGER-RNA SYNTHESIS BY SEQUENCE-SPECIFIC DNA-BINDING PROTEINS [J].
DYNAN, WS ;
TJIAN, R .
NATURE, 1985, 316 (6031) :774-778
[10]   CODING SEQUENCE AND GROWTH-REGULATION OF THE HUMAN VIMENTIN GENE [J].
FERRARI, S ;
BATTINI, R ;
KACZMAREK, L ;
RITTLING, S ;
CALABRETTA, B ;
DERIEL, JK ;
PHILIPONIS, V ;
WEI, JF ;
BASERGA, R .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (11) :3614-3620