IDENTIFICATION AND CHARACTERIZATION OF THROMBOSPONDIN-4, A NEW MEMBER OF THE THROMBOSPONDIN GENE FAMILY

被引:124
作者
LAWLER, J
DUQUETTE, M
WHITTAKER, CA
ADAMS, JC
MCHENRY, K
DESIMONE, DW
机构
[1] UNIV VIRGINIA, HLTH SCI CTR, DEPT ANAT & CELL BIOL, CHARLOTTESVILLE, VA 22908 USA
[2] UNIV VIRGINIA, HLTH SCI CTR, INST MOLEC BIOL, CHARLOTTESVILLE, VA 22908 USA
[3] HARVARD UNIV, SCH MED, BOSTON, MA 02115 USA
关键词
D O I
10.1083/jcb.120.4.1059
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A new member of the thrombospondin gene family, designated thrombospondin-4, has been identified in the Xenopus laevis genome. The predicted amino acid sequence indicates that the protein is similar to the other members of this gene family in the structure of the type 3 repeats and the COOH-terminal domain. Thrombospondin-4 contains four type 2 repeats and lacks the type 1 repeats that are found in thrombospondin-1 and 2. The amino-terminal domain of thrombospondin-4 has no significant homology with the other members of the thrombospondin gene family or with other proteins in the database. RNAse protection analysis establishes that the initial expression of Xenopus thrombospondin-4 is observed during neurulation. Levels of mRNA expression increase twofold during tailbud stages but decrease by the feeding tadpole stage. The size of the thrombospondin-4 message is 3.3 Kb and 3.4 Kb in the frog and human, respectively. Northern blot analysis of human tissues reveals high levels of thrombospondin-4 expression in heart and skeletal muscle, low levels in brain, lung and pancreas and undetectable levels in the placenta, liver and kidney. These data establish the existence of a new member of the thrombospondin gene family that may participate in the genesis and function of cardiac and skeletal muscle.
引用
收藏
页码:1059 / 1067
页数:9
相关论文
共 58 条
  • [1] THROMBOSPONDIN SEQUENCE MOTIF (CSVTCG) IS RESPONSIBLE FOR CD36-BINDING
    ASCH, AS
    SILBIGER, S
    HEIMER, E
    NACHMAN, RL
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 182 (03) : 1208 - 1217
  • [2] ASCH AS, 1991, J BIOL CHEM, V266, P1740
  • [3] ALBUMIN PHYLOGENY FOR CLAWED FROGS (XENOPUS)
    BISBEE, CA
    BAKER, MA
    WILSON, AC
    HADJIAZIMI, I
    FISCHBERG, M
    [J]. SCIENCE, 1977, 195 (4280) : 785 - 787
  • [4] BORNSTEIN P, 1990, J BIOL CHEM, V265, P16691
  • [5] BORNSTEIN P, 1991, J BIOL CHEM, V266, P12821
  • [6] A 2ND THROMBOSPONDIN GENE IN THE MOUSE IS SIMILAR IN ORGANIZATION TO THROMBOSPONDIN-1 BUT DOES NOT RESPOND TO SERUM
    BORNSTEIN, P
    DEVARAYALU, S
    LI, P
    DISTECHE, CM
    FRAMSON, P
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (19) : 8636 - 8640
  • [7] CELL ATTACHMENT AND FIBRINOGEN BINDING-PROPERTIES OF PLATELET AND ENDOTHELIAL-CELL THROMBOSPONDIN ARE NOT AFFECTED BY STRUCTURAL DIFFERENCES IN THE 70-KDA AND 18-KDA PROTEASE-RESISTANT DOMAINS
    CLEZARDIN, P
    BOURDILLON, MC
    HUNTER, NR
    MCGREGOR, JL
    [J]. FEBS LETTERS, 1988, 228 (02): : 215 - 218
  • [8] COLOCALIZATION OF THROMBOSPONDIN AND SYNDECAN DURING MURINE DEVELOPMENT
    CORLESS, CL
    MENDOZA, A
    COLLINS, T
    LAWLER, J
    [J]. DEVELOPMENTAL DYNAMICS, 1992, 193 (04) : 346 - 358
  • [9] DESIMONE DW, 1988, J BIOL CHEM, V263, P5333
  • [10] IDENTIFICATION AND CHARACTERIZATION OF ALTERNATIVELY SPLICED FIBRONECTIN MESSENGER-RNAS EXPRESSED IN EARLY XENOPUS EMBRYOS
    DESIMONE, DW
    NORTON, PA
    HYNES, RO
    [J]. DEVELOPMENTAL BIOLOGY, 1992, 149 (02) : 357 - 369