STRUCTURE AND EXPRESSION OF A SMOOTH-MUSCLE CELL-SPECIFIC GENE, SM22-ALPHA

被引:230
作者
SOLWAY, J [1 ]
SELTZER, J [1 ]
SAMAHA, FF [1 ]
KIM, S [1 ]
ALGER, LE [1 ]
NIU, Q [1 ]
MORRISEY, EE [1 ]
IP, HS [1 ]
PARMACEK, MS [1 ]
机构
[1] UNIV CHICAGO, DEPT MED, CHICAGO, IL 60637 USA
关键词
D O I
10.1074/jbc.270.22.13460
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
SM22 alpha is expressed exclusively in smooth muscle-containing tissues of adult animals and is one of the earliest markers of differentiated smooth muscle cells (SMCs). To examine the molecular mechanisms that regulate SMC-specific gene expression, Foe have isolated and structurally characterized the murine SM22 alpha gene. SM22 alpha is a 6.2-kilobase single copy gene composed of five exons. SM22 alpha mRNA is expressed at high levels in the aorta, uterus, lung, and intestine, and in primary cultures of rat aortic SMCs, and the SMC line, A7r5. ln contrast to genes encoding SMC contractile proteins, SM22 alpha gene expression is not decreased in proliferating SMCs. Transient transfection experiments demonstrated that 441 base pairs of SM22 alpha 5'-flanking sequence was necessary and sufficient to program high level transcription of a luciferase reporter gene in both primary rat aortic SMCs and A7r5 cells. DNA sequence analyses revealed that the 441-base pair promoter contains two CArG/SRF boxes, a CACC box, and one potential MEF-2 binding site, cis-acting elements which are each important regulators of striated muscle transcription. Taken together, these studies have identified the murine SM22 alpha promoter as an excellent model system for studies of developmentally regulated, Lineage-specific gene expression in SMCs.
引用
收藏
页码:13460 / 13469
页数:10
相关论文
共 70 条
  • [1] HUMAN SMOOTH-MUSCLE MYOSIN HEAVY-CHAIN ISOFORMS AS MOLECULAR MARKERS FOR VASCULAR DEVELOPMENT AND ATHEROSCLEROSIS
    AIKAWA, M
    SIVAM, PN
    KUROO, M
    KIMURA, K
    NAKAHARA, K
    TAKEWAKI, S
    UEDA, M
    YAMAGUCHI, H
    YAZAKI, Y
    PERIASAMY, M
    NAGAI, R
    [J]. CIRCULATION RESEARCH, 1993, 73 (06) : 1000 - 1012
  • [2] A NUCLEAR FACTOR FOR IL-6 EXPRESSION (NF-IL6) IS A MEMBER OF A C/EBP FAMILY
    AKIRA, S
    ISSHIKI, H
    SUGITA, T
    TANABE, O
    KINOSHITA, S
    NISHIO, Y
    NAKAJIMA, T
    HIRANO, T
    KISHIMOTO, T
    [J]. EMBO JOURNAL, 1990, 9 (06) : 1897 - 1906
  • [3] CHARACTERIZATION OF THE GENE FOR MP20 - A DROSOPHILA MUSCLE PROTEIN THAT IS NOT FOUND IN ASYNCHRONOUS OSCILLATORY FLIGHT-MUSCLE
    AYMESOUTHGATE, A
    LASKO, P
    FRENCH, C
    PARDUE, ML
    [J]. JOURNAL OF CELL BIOLOGY, 1989, 108 (02) : 521 - 531
  • [4] BELKIN AM, 1988, J BIOL CHEM, V263, P6631
  • [5] BLANK RS, 1992, J BIOL CHEM, V267, P984
  • [6] BREATHNACH R, 1981, ANNU REV BIOCHEM, V50, P349, DOI 10.1146/annurev.bi.50.070181.002025
  • [7] CARROLL SL, 1986, J BIOL CHEM, V261, P8965
  • [8] CYTOSTATIC GENE-THERAPY FOR VASCULAR PROLIFERATIVE DISORDERS WITH A CONSTITUTIVELY ACTIVE FORM OF THE RETINOBLASTOMA GENE-PRODUCT
    CHANG, MW
    BARR, E
    SELTZER, J
    JIANG, YQ
    NABEL, GJ
    NABEL, EG
    PARMACEK, MS
    LEIDEN, JM
    [J]. SCIENCE, 1995, 267 (5197) : 518 - 522
  • [9] MODULATION OF GELSOLIN CONTENT IN RAT AORTIC SMOOTH-MUSCLE CELLS DURING DEVELOPMENT, EXPERIMENTAL INTIMAL THICKENING AND CULTURE - AN IMMUNOHISTOCHEMICAL AND BIOCHEMICAL-STUDY
    CHAPONNIER, C
    KOCHER, O
    GABBIANI, G
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1990, 190 (03): : 559 - 565
  • [10] CHOMCZYNSKI P, 1993, BIOTECHNIQUES, V15, P532