Developmental expression and activities of specific Fos and Jun proteins are functionally related to osteoblast maturation: Role of Fra-2 and Jun D during differentiation

被引:158
作者
McCabe, LR
Banerjee, C
Kundu, R
Harrison, RJ
Dobner, PR
Stein, JL
Lian, JB
Stein, GS
机构
[1] UNIV MASSACHUSETTS, MED CTR, CTR CANC, WORCESTER, MA 01655 USA
[2] UNIV MASSACHUSETTS, MED CTR, DEPT MOL GENET & MICROBIOL, WORCESTER, MA 01655 USA
关键词
D O I
10.1210/en.137.10.4398
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Developmental studies of oncogene expression implicate the Fos and Jun family of transcription Factors in the regulation of bone growth and differentiation. Promoters of many developmentally regulated genes, including osteocalcin, a marker of osteoblast differentiation, contain AP-1 sites that bind Fos/Jun dimers. Here, we demonstrate that the selective expression of fos- and jun-related genes is functionally related to the stage of osteoblast growth and differentiation in vitro. During osteoblast proliferation, nuclear protein levels of all seven activating protein-1 (AP-1) members are maximal. Subsequently, during the period of extracellular matrix maturation, levels decline. In fully differentiated osteoblasts, Fra-2 and (to a lesser extent) Jun D are the principal AP-1 members detectable by Western blot analysis. AFP-1 complex composition and binding activity also exhibit developmental changes. All Fos and Jun family members are involved in AP-1 complex formation in proliferating cells, whereas Fra-2 and Jun D predominate in AP-1 complexes in differentiated osteoblasts. Overexpression of Fos and Jun family members in ROS 17/2.8 cells markedly affects the expression of an osteocalcin promoter-chloramphenicol acetyltransferase construct. Coexpression of only one AP-1 pair, Fra-2 and Jun D, stimulated reporter expression, whereas coexpression of other AP-1 pairs down-regulated expression (i.e. c-jun and any Fos family member) or had no effect (i.e. Fra-1 and Jun B). Promoter deletion analyses indicate that these effects are site specific. Consequential effects of Fra-2 on osteoblast differentiation are further demonstrated by antisense studies in which osteoblast differentiation and the development of a bone tissue-like organization were suppressed. Consistent with recent findings suggesting that AP-1 complex composition can selectively regulate gene transcription, our findings demonstrate that differential expression of Fos and Jun family members could play a role in the developmental regulation of bone-specific gene expression and, as a result, may be functionally significant for osteoblast differentiation.
引用
收藏
页码:4398 / 4408
页数:11
相关论文
共 57 条
[1]   THE ROLE OF JUN, FOS AND THE AP-1 COMPLEX IN CELL-PROLIFERATION AND TRANSFORMATION [J].
ANGEL, P ;
KARIN, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1072 (2-3) :129-157
[2]   FACTORS THAT PROMOTE PROGRESSIVE DEVELOPMENT OF THE OSTEOBLAST PHENOTYPE IN CULTURED FETAL-RAT CALVARIA CELLS [J].
ARONOW, MA ;
GERSTENFELD, LC ;
OWEN, TA ;
TASSINARI, MS ;
STEIN, GS ;
LIAN, JB .
JOURNAL OF CELLULAR PHYSIOLOGY, 1990, 143 (02) :213-221
[3]   CONTRIBUTIONS OF DISTAL AND PROXIMAL PROMOTER ELEMENTS TO GLUCOCORTICOID REGULATION OF OSTEOCALCIN GENE-TRANSCRIPTION [J].
ASLAM, F ;
SHALHOUB, V ;
VANWIJNEN, AJ ;
BANERJEE, C ;
BORTELL, R ;
SHAKOORI, AR ;
LITWACK, G ;
STEIN, JL ;
STEIN, GS ;
LIAN, JB .
MOLECULAR ENDOCRINOLOGY, 1995, 9 (06) :679-690
[4]  
Ausubel FA, 1995, CURRENT PROTOCOLS MO
[5]   Transforming growth factor-beta 1 responsiveness of the rat osteocalcin gene is mediated by an activator protein-1 binding site [J].
Banerjee, C ;
Stein, JL ;
VanWijnen, AJ ;
Frenkel, B ;
Lian, JB ;
Stein, GS .
ENDOCRINOLOGY, 1996, 137 (05) :1991-2000
[6]   An AML-1 consensus sequence binds an osteoblast-specific complex and transcriptionally activates the osteocalcin gene [J].
Banerjee, C ;
Hiebert, SW ;
Stein, JL ;
Lian, JB ;
Stein, GS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (10) :4968-4973
[7]   MINERALIZED BONE NODULES FORMED INVITRO FROM ENZYMATICALLY RELEASED RAT CALVARIA CELL-POPULATIONS [J].
BELLOWS, CG ;
AUBIN, JE ;
HEERSCHE, JNM ;
ANTOSZ, ME .
CALCIFIED TISSUE INTERNATIONAL, 1986, 38 (03) :143-154
[8]   PHYSIOLOGICAL CONCENTRATIONS OF GLUCOCORTICOIDS STIMULATE FORMATION OF BONE NODULES FROM ISOLATED RAT CALVARIA CELLS-INVITRO [J].
BELLOWS, CG ;
AUBIN, JE ;
HEERSCHE, JNM .
ENDOCRINOLOGY, 1987, 121 (06) :1985-1992
[9]   FUNCTIONAL-ROLE FOR SP1 IN THE TRANSCRIPTIONAL AMPLIFICATION OF A CELL-CYCLE-REGULATED HISTONE H4 GENE [J].
BIRNBAUM, MJ ;
WRIGHT, KL ;
VANWIJNEN, AJ ;
RAMSEYEWING, AL ;
BOURKE, MT ;
LAST, TJ ;
AZIZ, F ;
FRENKEL, B ;
RAO, BR ;
ARONIN, N ;
STEIN, GS ;
STEIN, JL .
BIOCHEMISTRY, 1995, 34 (23) :7648-7658
[10]   VITAMIN-D-RESPONSIVE PROTEIN DNA INTERACTIONS AT MULTIPLE PROMOTER REGULATORY ELEMENTS THAT CONTRIBUTE TO THE LEVEL OF RAT OSTEOCALCIN GENE-EXPRESSION [J].
BORTELL, R ;
OWEN, TA ;
BIDWELL, JP ;
GAVAZZO, P ;
BREEN, E ;
VANWIJNEN, AJ ;
DELUCA, HF ;
STEIN, JL ;
LIAN, JB ;
STEIN, GS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (13) :6119-6123