SEQUENCE-SPECIFIC BINDING OF HMG-I(Y) TO THE PROXIMAL PROMOTER OF THE GP91-PHOX GENE

被引:22
作者
SKALNIK, DG [1 ]
NEUFELD, EJ [1 ]
机构
[1] HARVARD UNIV,CHILDRENS HOSP,SCH MED,DANA FARBER CANC INST,DEPT PEDIAT,DIO HEMATOL ONCOL,BOSTON,MA 02115
基金
美国国家卫生研究院;
关键词
D O I
10.1016/0006-291X(92)91231-E
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
Screening of a cDNA expression library with a CCAAT-box element derived from the myelomonocyte-specific gp91-phox promoter resulted in the isolation of three independent HMG-I(Y) cDNA clones. Filter binding competition studies reveal that HMG-Y binds to this promoter element in a sequence-specific manner and exhibits a gradient of binding affinities for various A T-rich sequences. Two adjacent A T-rich regions within the gp91-phox promoter CCAAT-box element are required for maximal binding. In addition, competition experiments demonstrate that the binding affinity of HMG-Y is influenced by sequences that flank A T-rich core binding sites. © 1992.
引用
收藏
页码:563 / 569
页数:7
相关论文
共 26 条
[1]  
AMNFIOLETTI G, 1991, NUC ACIDS RES, V19, P6793
[2]   CLONING OF CDNAS CODING FOR HUMAN HMG-I AND HMG-Y PROTEINS - BOTH ARE CAPABLE OF BINDING TO THE OCTAMER SEQUENCE MOTIF [J].
ECKNER, R ;
BIRNSTIEL, ML .
NUCLEIC ACIDS RESEARCH, 1989, 17 (15) :5947-5959
[3]  
EMIJER L, 1991, EUR J BIOCHEM, V196, P557
[4]   ANALYSIS OF THE HMGI NUCLEAR PROTEINS IN MOUSE NEOPLASTIC-CELLS INDUCED BY DIFFERENT PROCEDURES [J].
GIANCOTTI, V ;
BURATTI, E ;
PERISSIN, L ;
ZORZET, S ;
BALMAIN, A ;
PORTELLA, G ;
FUSCO, A ;
GOODWIN, GH .
EXPERIMENTAL CELL RESEARCH, 1989, 184 (02) :538-545
[5]   ELEVATED LEVELS OF A SPECIFIC CLASS OF NUCLEAR PHOSPHOPROTEINS IN CELLS TRANSFORMED WITH V-RAS AND V-MOS ONCOGENES AND BY COTRANSFECTION WITH C-MYC AND POLYOMA MIDDLE T-GENES [J].
GIANCOTTI, V ;
PANI, B ;
DANDREA, P ;
BERLINGIERI, MT ;
DIFIORE, PP ;
FUSCO, A ;
VECCHIO, G ;
PHILP, R ;
CRANEROBINSON, C ;
NICOLAS, RH ;
WRIGHT, CA ;
GOODWIN, GH .
EMBO JOURNAL, 1987, 6 (07) :1981-1987
[6]   THE HMG DOMAIN OF LYMPHOID ENHANCER FACTOR-I BENDS DNA AND FACILITATES ASSEMBLY OF FUNCTIONAL NUCLEOPROTEIN STRUCTURES [J].
GIESE, K ;
COX, J ;
GROSSCHEDL, R .
CELL, 1992, 69 (01) :185-195
[7]   ALTERNATIVE PROCESSING OF MESSENGER-RNAS ENCODING MAMMALIAN CHROMOSOMAL HIGH-MOBILITY-GROUP PROTEINS HMG-I AND HMG-Y [J].
JOHNSON, KR ;
LEHN, DA ;
REEVES, R .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (05) :2114-2123
[8]  
JOHNSON KR, 1988, J BIOL CHEM, V263, P18338
[9]   THE AMINO-ACID SEQUENCE OF THE CHROMOSOMAL PROTEIN HMG-Y, ITS RELATION TO HMG-I AND POSSIBLE DOMAINS FOR THE PREFERENTIAL BINDING OF THE PROTEINS TO STRETCHES OF A-T BASE-PAIRS [J].
KARLSON, JR ;
MORK, E ;
HOLTLUND, J ;
LALAND, SG ;
LUND, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 158 (03) :646-651
[10]   INTERACTION OF TFIID IN THE MINOR GROOVE OF THE TATA ELEMENT [J].
LEE, DK ;
HORIKOSHI, M ;
ROEDER, RG .
CELL, 1991, 67 (06) :1241-1250