POSITION AND ORIENTATION-SELECTIVE SILENCER IN PROTEIN-CODING SEQUENCES OF THE RAT OSTEOCALCIN GENE

被引:34
作者
FRENKEL, B
MIJNES, J
ARONOW, MA
ZAMBETTI, G
BANERJEE, C
STEIN, JL
LIAN, JB
STEIN, GS
机构
[1] UNIV MASSACHUSETTS,MED CTR,DEPT CELL BIOL,55 LAKE AVE N,WORCESTER,MA 01655
[2] UNIV MASSACHUSETTS,MED CTR,DEPT ORTHOPED SURG,WORCESTER,MA 01655
关键词
D O I
10.1021/bi00212a031
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
Osteocalcin (OC) is a bone-specific protein which is expressed postproliferatively by osteoblasts during late stages of differentiation. We have found that a silencer element is present within the rat OC gene (between nt +39 and +104), overlapping the OC signal prepropeptide-coding sequence. The presence of this sequence in OC promoter-CAT reporter constructs suppresses promoter activity in transiently transfected proliferating osteoblasts, which do not express OC, by up to 50-fold. This is the first demonstration of contribution from protein-coding sequences to silencing of animal genes. The element appears to be bipartite; silencer activity requires both the protein-coding sequence +39 to +63 and the +93 to +104 exon 1/intron 1 border region. Both of these domains contain sequences highly similar to silencer motifs in several other genes, including chicken lysozyme as well as rat collagen type II, insulin, and growth hormone. OC silencer activity is fully retained when the element is placed outside the RNA-coding region, 3' but not 5' of the OC-CAT fusion gene. Repression activity is orientation independent in the native position but requires the native orientation when located in 3' extragenic positions. The silencer does not inhibit the activity of the heterologous SV40 early promoter. These results suggest interaction between the transcribed silencer and specific OC promoter element(s) residing farther upstream. The OC transcribed silencer may contribute to developmental control of OC expression.
引用
收藏
页码:13636 / 13643
页数:8
相关论文
共 53 条
[1]   LOCALIZATION OF TRANSCRIPTIONAL REGULATORY ELEMENTS AND NUCLEAR FACTOR BINDING-SITES IN MOUSE RIBOSOMAL-PROTEIN GENE RPL32 [J].
ATCHISON, ML ;
MEYUHAS, O ;
PERRY, RP .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (05) :2067-2074
[2]  
Ausubel F, 1988, CURRENT PROTOCOLS MO
[3]   KINDRED S-THYROID HORMONE RECEPTOR IS AN ACTIVE AND CONSTITUTIVE SILENCER AND A REPRESSOR FOR THYROID-HORMONE AND RETINOIC ACID RESPONSES [J].
BANIAHMAD, A ;
TSAI, SY ;
OMALLEY, BW ;
TSAI, MJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (22) :10633-10637
[4]   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
[5]   MODULAR STRUCTURE OF A CHICKEN LYSOZYME SILENCER - INVOLVEMENT OF AN UNUSUAL THYROID-HORMONE RECEPTOR-BINDING SITE [J].
BANIAHMAD, A ;
STEINER, C ;
KOHNE, AC ;
RENKAWITZ, R .
CELL, 1990, 61 (03) :505-514
[6]   CHARACTERIZATION AND PURIFICATION OF ADH DISTAL PROMOTER FACTOR-2, ADF-2, A CELL-SPECIFIC AND PROMOTER-SPECIFIC REPRESSOR IN DROSOPHILIA [J].
BENYAJATI, C ;
EWEL, A ;
MCKEON, J ;
CHOVAV, M ;
JUAN, E .
NUCLEIC ACIDS RESEARCH, 1992, 20 (17) :4481-4489
[7]   CHARACTERIZATION OF A SILENCER IN YEAST - A DNA-SEQUENCE WITH PROPERTIES OPPOSITE TO THOSE OF A TRANSCRIPTIONAL ENHANCER [J].
BRAND, AH ;
BREEDEN, L ;
ABRAHAM, J ;
STERNGLANZ, R ;
NASMYTH, K .
CELL, 1985, 41 (01) :41-48
[8]   IDENTIFICATION OF A TRANSCRIPTIONAL SILENCER IN THE 5'-FLANKING REGION OF THE HUMAN EPSILON-GLOBIN GENE [J].
CAO, SX ;
GUTMAN, PD ;
DAVE, HPG ;
SCHECHTER, AN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (14) :5306-5309
[9]   NEGATIVE CONTROL OF LIVER-SPECIFIC GENE-EXPRESSION - CLONED HUMAN RETINOL-BINDING PROTEIN GENE IS REPRESSED IN HELA-CELLS [J].
COLANTUONI, V ;
PIROZZI, A ;
BLANCE, C ;
CORTESE, R .
EMBO JOURNAL, 1987, 6 (03) :631-636
[10]   DNA-SEQUENCES IN THE RAT OSTEOCALCIN GENE THAT BIND THE 1,25-DIHYDROXYVITAMIN-D3 RECEPTOR AND CONFER RESPONSIVENESS TO 1,25-DIHYDROXYVITAMIN-D3 [J].
DEMAY, MB ;
GERARDI, JM ;
DELUCA, HF ;
KRONENBERG, HM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (01) :369-373