Direct evidence that the POU family transcription factor Oct-2 represses the cellular tyrosine hydroxylase gene in neuronal cells

被引:12
作者
Deans, L
Dawson, SJ
Buttery, L
Polak, JM
Wallace, D
Latchman, DS
机构
[1] UCL, SCH MED, DEPT MOLEC PATHOL, LONDON W1N 8AA, ENGLAND
[2] HAMMERSMITH HOSP, ROYAL POSTGRAD MED SCH, DEPT HISTOCHEM, LONDON W12 0HS, ENGLAND
[3] GLAXO RES & DEV LTD, MED RES CTR, STEVENAGE, HERTS, ENGLAND
关键词
Oct-2 transcription factor; tyrosine hydroxylase; gene repression;
D O I
10.1007/BF02736762
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
The POU family transcription factor Oct-2 was originally identified in B lymphocytes but has been shown to be expressed in neuronal cells, although it is absent in most other cell types. Cotransfection of Oct-2 expression vectors into nonneuronal cells with a tyrosine hydroxylase promoter/reporter plasmid suggests that Oct-2 can repress this promoter in this artificial situation. Here we report that reduction of endogenous Oct-2 levels in a neuronal cell line by an antisense approach results in an increase in endogenous tyrosine hydroxylase levels. In contrast, the level of the neuronal marker protein PGP9.5 remains unchanged in the antisense lines whereas that of the neuronal nitric oxide synthase decreases. Hence, the tyrosine hydroxylase gene is a natural target for repression by Oct-2 in neuronal cells. The significance of this effect is discussed in terms of the processes that regulate tyrosine hydroxylase gene expression and the role of Oct-2 in neuronal cells.
引用
收藏
页码:159 / 167
页数:9
相关论文
共 39 条
[1]  
BJORKLUND A, 1984, HDB CHEM NEUROANAT 1
[2]   EPIDERMAL GROWTH-FACTOR INDUCES, IN THE EL-ALPHA-4-2 CELL-LINE, HERPES-SIMPLEX VIRUS-1 ALPHA-4 GENE-TRANSCRIPTION IN THE ABSENCE OF THE VIRAL TRANSACTIVATOR VP16 [J].
BOVOLENTA, C ;
TOGNON, M ;
LIBOI, E .
VIRUS RESEARCH, 1991, 19 (2-3) :199-208
[3]   THE OCT-2 TRANSCRIPTION FACTOR REPRESSES TYROSINE-HYDROXYLASE EXPRESSION VIA A HEPTAMER TAATGARAT-LIKE MOTIF IN THE GENE PROMOTER [J].
DAWSON, SJ ;
YOON, SO ;
CHIKARAISHI, DM ;
LILLYCROP, KA ;
LATCHMAN, DS .
NUCLEIC ACIDS RESEARCH, 1994, 22 (06) :1023-1028
[4]   THE B-CELL AND NEURONAL FORMS OF THE OCTAMER-BINDING PROTEIN OCT-2 DIFFER IN DNA-BINDING SPECIFICITY AND FUNCTIONAL-ACTIVITY [J].
DENT, CL ;
LILLYCROP, KA ;
ESTRIDGE, JK ;
THOMAS, NSB ;
LATCHMAN, DS .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (08) :3925-3930
[5]   DIFFERENTIAL HEAT-SHOCK PROTEIN OVEREXPRESSION AND ITS CLINICAL RELEVANCE IN SYSTEMIC LUPUS-ERYTHEMATOSUS [J].
DHILLON, VB ;
MCCALLUM, S ;
NORTON, P ;
TWOMEY, BM ;
ERKELLERYUKSEL, F ;
LYDYARD, P ;
ISENBERG, DA ;
LATCHMAN, DS .
ANNALS OF THE RHEUMATIC DISEASES, 1993, 52 (06) :436-442
[6]  
FALKNER FG, 1986, NUCLEIC ACIDS RES, V13, P7847
[7]   CELL TYPE-SPECIFICITY ELEMENTS OF THE IMMUNOGLOBULIN HEAVY-CHAIN GENE ENHANCER [J].
GERSTER, T ;
MATTHIAS, P ;
THALI, M ;
JIRICNY, J ;
SCHAFFNER, W .
EMBO JOURNAL, 1987, 6 (05) :1323-1330
[8]   NEGATIVE EFFECT OF THE TRANSCRIPTIONAL ACTIVATOR GAL4 [J].
GILL, G ;
PTASHNE, M .
NATURE, 1988, 334 (6184) :721-724
[9]  
Gorman C., 1985, DNA CLONING PRACTICA, V1, P143
[10]  
KATZ DM, 1991, J NEUROSCI, V11, P3991