THE OCT-2 TRANSCRIPTION FACTOR REPRESSES TYROSINE-HYDROXYLASE EXPRESSION VIA A HEPTAMER TAATGARAT-LIKE MOTIF IN THE GENE PROMOTER

被引:38
作者
DAWSON, SJ
YOON, SO
CHIKARAISHI, DM
LILLYCROP, KA
LATCHMAN, DS
机构
[1] UCL, SCH MED, DEPT MOLEC PATHOL, LONDON W1P 6DB, ENGLAND
[2] UCL, SCH MED, DEPT MOLEC BIOL & MICROBIOL, LONDON W1P 6DB, ENGLAND
[3] TUFTS UNIV, SCH MED, PROGRAM NEUROSCI, BOSTON, MA 02111 USA
基金
英国医学研究理事会;
关键词
D O I
10.1093/nar/22.6.1023
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 tyrosine hydroxylase (TH) gene promoter contains adjacent octamer and heptamer motifs which act as target sites for octamer binding transcription factors. Mutation of the heptamer motif but not the octamer motif enhances TH promoter activity in neuronal cells expressing Oct-2 but not in non-expressing fibroblasts. Similarly addition of the heptamer motif to a minimal TH promoter represses gene expression in neuronal cells but not in fibroblasts. These effects can be reproduced by the artificial expression of neuronal isoforms of Oct-2 in fibroblasts which results in the repression of transfected TH promoters containing an intact heptamer motif but not those in which this motif has been mutated or deleted. The TH promoter thus represents the first example of a cellular promoter which is repressed by Oct-2. The significance of this effect is discussed in terms of the cell type specificity of the TH promoter and its induction by different physiological stimuli.
引用
收藏
页码:1023 / 1028
页数:6
相关论文
共 39 条
[1]   A PROCEDURE TO STANDARDIZE CAT REPORTER GENE ASSAY [J].
ABKEN, H ;
REIFENRATH, B .
NUCLEIC ACIDS RESEARCH, 1992, 20 (13) :3527-3527
[2]   OCT2 TRANSACTIVATION FROM A REMOTE ENHANCER POSITION REQUIRES A B-CELL-RESTRICTED ACTIVITY [J].
ANNWEILER, A ;
MULLERIMMERGLUCK, M ;
WIRTH, T .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (07) :3107-3116
[3]  
Bjorklund A., 1984, HDB CHEM NEUROANATOM, V2, P55
[4]   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
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   5' FLANKING DNA-SEQUENCES DIRECT CELL-SPECIFIC EXPRESSION OF RAT TYROSINE-HYDROXYLASE [J].
CAMBI, F ;
FUNG, B ;
CHIKARAISHI, D .
JOURNAL OF NEUROCHEMISTRY, 1989, 53 (05) :1656-1659
[7]   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
[8]  
FALKNER FG, 1986, NUCLEIC ACIDS RES, V13, P7847
[9]   SEQUENCES THAT DIRECT RAT TYROSINE-HYDROXYLASE GENE-EXPRESSION [J].
FUNG, BP ;
YOON, SO ;
CHIKARAISHI, DM .
JOURNAL OF NEUROCHEMISTRY, 1992, 58 (06) :2044-2052
[10]   NERVE GROWTH-FACTOR REGULATES TYROSINE-HYDROXYLASE GENE-TRANSCRIPTION THROUGH A NUCLEOPROTEIN COMPLEX THAT CONTAINS C-FOS [J].
GIZANGGINSBERG, E ;
ZIFF, EB .
GENES & DEVELOPMENT, 1990, 4 (04) :477-491