TRANSCRIPTIONAL REGULATION OF THE CHICKEN CALDESMON GENE - ACTIVATION OF GIZZARD-TYPE CALDESMON PROMOTER REQUIRES A CARG BOX-LIKE MOTIF

被引:54
作者
YANO, H [1 ]
HAYASHI, K [1 ]
MOMIYAMA, T [1 ]
SAGA, H [1 ]
HARUNA, M [1 ]
SOBUE, K [1 ]
机构
[1] OSAKA UNIV,SCH MED,BIOMED RES CTR,DEPT NEUROCHEM & NEUROPHARMACOL,SUITA,OSAKA 565,JAPAN
关键词
D O I
10.1074/jbc.270.40.23661
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
Caldesmon, which plays a vital role in the actomyosin system, is distributed in smooth muscle and non-muscle cells, and its isoformal interconversion between a high M(r) form and low M(r) form is a favorable molecular event for studying phenotypic modulation of smooth muscle cells. Genomic analysis reveals two promoters, of which the gizzard-type promoter displays much higher activity than the brain-type promoter. Here, we have characterized transcriptional regulation of the gizzard-type promoter. Transient transfection assays in chick gizzard smooth muscle cells, chick embryo fibroblasts, mouse skeletal muscle cell line (C2C12), and HeLa cells revealed that the promoter activity was high in smooth muscle cells and fibroblasts, but was extremely low in other cells. Cell type-specific promoter activity depended on an element, CArG1, containing a unique CArG box-like motif (CCAAAAAAGG) at -315, while multiple E boxes were not directly involved in this event. Gel shift assays showed the specific interaction between the CArG1 and nuclear protein factors in smooth muscle cells and fibroblasts. These results suggest that the CArG1 is an essential cis element for cell type specific expression of caldesmon and that the function of CArG1 might be controlled under phenotypic modulation of smooth muscle cells.
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页码:23661 / 23666
页数:6
相关论文
共 43 条
[1]   SYNTHESIS AND EXPRESSION OF SMOOTH-MUSCLE PHENOTYPE MARKERS IN PRIMARY CULTURE OF RABBIT AORTIC SMOOTH-MUSCLE CELLS - INFLUENCE OF SEEDING DENSITY AND MEDIA AND RELATION TO CELL CONTRACTILITY [J].
BIRUKOV, KG ;
FRID, MG ;
ROGERS, JD ;
SHIRINSKY, VP ;
KOTELIANSKY, VE ;
CAMPBELL, JH ;
CAMPBELL, GR .
EXPERIMENTAL CELL RESEARCH, 1993, 204 (01) :46-53
[2]  
BLANK RS, 1992, J BIOL CHEM, V267, P984
[3]   CYTOPLASMIC ACTIVATION OF HUMAN NUCLEAR GENES IN STABLE HETEROCARYONS [J].
BLAU, HM ;
CHIU, CP ;
WEBSTER, C .
CELL, 1983, 32 (04) :1171-1180
[4]   RECENT ADVANCES IN MOLECULAR PATHOLOGY - SMOOTH-MUSCLE PHENOTYPIC CHANGES IN ARTERIAL-WALL HOMEOSTASIS - IMPLICATIONS FOR THE PATHOGENESIS OF ATHEROSCLEROSIS [J].
CAMPBELL, GR ;
CAMPBELL, JH .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 1985, 42 (02) :139-162
[5]   FIREFLY LUCIFERASE GENE - STRUCTURE AND EXPRESSION IN MAMMALIAN-CELLS [J].
DEWET, JR ;
WOOD, KV ;
DELUCA, M ;
HELINSKI, DR ;
SUBRAMANI, S .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (02) :725-737
[6]   IDENTIFICATION BY MONOCLONAL-ANTIBODIES AND CHARACTERIZATION OF HUMAN-PLATELET CALDESMON [J].
DINGUS, J ;
HWO, S ;
BRYAN, J .
JOURNAL OF CELL BIOLOGY, 1986, 102 (05) :1748-1757
[7]  
DRAEGER A, 1989, J CELL SCI, V94, P703
[8]   SPECIFIC STIMULATION OF ACTIN GENE-TRANSCRIPTION BY EPIDERMAL GROWTH-FACTOR AND CYCLOHEXIMIDE [J].
ELDER, PK ;
SCHMIDT, LJ ;
ONO, T ;
GETZ, MJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (23) :7476-7480
[9]  
FOSTER DN, 1992, J BIOL CHEM, V267, P11995
[10]   CALPONIN AND SM-22 ISOFORMS IN AVIAN AND MAMMALIAN SMOOTH-MUSCLE - ABSENCE OF PHOSPHORYLATION INVIVO [J].
GIMONA, M ;
SPARROW, MP ;
STRASSER, P ;
HERZOG, M ;
SMALL, JV .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 205 (03) :1067-1075