A DEVELOPMENTALLY REGULATED DNA-BINDING PROTEIN FROM MOUSE-BRAIN STIMULATES MYELIN BASIC-PROTEIN GENE-EXPRESSION

被引:60
作者
HAAS, S [1 ]
GORDON, J [1 ]
KHALILI, K [1 ]
机构
[1] THOMAS JEFFERSON UNIV, JEFFERSON INST MOLEC MED, DEPT BIOCHEM & MOLEC BIOL, PHILADELPHIA, PA 19107 USA
关键词
D O I
10.1128/MCB.13.5.3103
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
Transcription of the myelin basic protein (MBP) gene is regulated in a cell-type-specific and developmental stage-specific manner during myelin formation in the murine central nervous system. The 5'-flanking region of the MBP gene contains several regulatory elements that differentially contribute to the cell-type-specific transcription of MBP in cells derived from the central nervous system. The proximal element, termed MB1, which is located between nucleotides -14 and -50 with respect to the RNA start site, has previously been shown to have characteristics of a cell-type-specific enhancer element. In this study, we used band shift and UV cross-linking assays to identify DNA-binding proteins in mouse brain nuclear extract which interact with the MB1 element. Fractionation of these extracts has allowed the identification of a 38- to 41-kDa nuclear protein, derived from mouse brain tissue at the peak of myelination, which specifically binds the MB1 DNA sequence. Fractions enriched in the MB1-binding protein have been shown to stimulate transcription of the MBP promoter in extract derived from HeLa cells. MB1 binding protein activity is expressed in a tissue-specific and developmental stage-specific pattern which coincides with the pattern of MBP transcription, suggesting that this protein may be a biologically relevant transcription factor for the MBP gene in vivo.
引用
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页码:3103 / 3112
页数:10
相关论文
共 47 条
[1]  
AHMED S, 1990, J BIOL CHEM, V265, P13899
[2]  
Ausubel F, 1988, CURRENT PROTOCOLS MO
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]   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
[5]   CELLULAR AND MOLECULAR ASPECTS OF MYELIN PROTEIN GENE-EXPRESSION [J].
CAMPAGNONI, AT ;
MACKLIN, WB .
MOLECULAR NEUROBIOLOGY, 1988, 2 (01) :41-89
[6]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[7]   FORMATION OF STABLE PRE-INITIATION COMPLEXES BETWEEN EUKARYOTIC CLASS-B TRANSCRIPTION FACTORS AND PROMOTER SEQUENCES [J].
DAVISON, BL ;
EGLY, JM ;
MULVIHILL, ER ;
CHAMBON, P .
NATURE, 1983, 301 (5902) :680-686
[8]   ALTERNATIVE SPLICING ACCOUNTS FOR THE 4 FORMS OF MYELIN BASIC-PROTEIN [J].
DEFERRA, F ;
ENGH, H ;
HUDSON, L ;
KAMHOLZ, J ;
PUCKETT, C ;
MOLINEAUX, S ;
LAZZARINI, RA .
CELL, 1985, 43 (03) :721-727
[9]  
DESCHAMPS J, 1992, Critical Reviews in Oncogenesis, V3, P117
[10]  
DEVINEBEACH K, 1990, J BIOL CHEM, V265, P13830