BMP-7 IS AN INDUCER OF NEPHROGENESIS, AND IS ALSO REQUIRED FOR EYE DEVELOPMENT AND SKELETAL PATTERNING

被引:821
作者
LUO, G
HOFMANN, C
BRONCKERS, ALJJ
SOHOCKI, M
BRADLEY, A
KARSENTY, G
机构
[1] UNIV TEXAS,MD ANDERSON CANC CTR,DEPT MOLEC GENET,HOUSTON,TX 77030
[2] BAYLOR COLL MED,DEPT BIOCHEM,HOUSTON,TX 77030
[3] BAYLOR COLL MED,HOWARD HUGHES MED INST,DEPT MOLEC & HUMAN GENET,HOUSTON,TX 77030
[4] GSF,FORSCHUNGSZENTRUM UMWELT & GESUNDHEIT,INST SAEUGETIERGENET,D-85758 OBERSCHLEISSHEIM,GERMANY
关键词
BMP-7; KIDNEY EYE; LIMB;
D O I
10.1101/gad.9.22.2808
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Bone morphogenetic proteins (BMPs) are multifunctional growth factors originally identified by their ability to induce ectopic bone formation. To investigate the function of one of the BMPs, BMP-7, we have generated BMP-7-deficient mice using embryonic stem cell technology. BMP-7-deficient mice die shortly after birth because of poor kidney development. Histological analysis of mutant embryos at several stages of development revealed that metanephric mesenchymal cells fail to differentiate, resulting in a virtual absence of glomerulus in newborn kidneys. In situ hybridization analysis showed that the absence of BMP-7 affects the expression of molecular markers of nephrogenesis, such as Pax-2 and Wnt-4 between 12.5 and 14.5 days postcoitum (dpc). This identifies BMP-7 as an inducer of nephrogenesis. In addition, BMP-7-deficient mice have eye defects that appear to originate during lens induction. Finally, BMP-7-deficient mice also have skeletal patterning defects restricted to the rib cage, the skull, and the hindlimbs.
引用
收藏
页码:2808 / 2820
页数:13
相关论文
共 58 条
  • [1] [Anonymous], 1987, TERATOCARCINOMA EMBR
  • [2] ARMSTRONG JF, 1992, MECH DEVELOP, V40, P85
  • [3] ISOLATION AND CHARACTERIZATION OF A ZINC FINGER POLYPEPTIDE GENE AT THE HUMAN CHROMOSOME-11 WILMS TUMOR LOCUS
    CALL, KM
    GLASER, T
    ITO, CY
    BUCKLER, AJ
    PELLETIER, J
    HABER, DA
    ROSE, EA
    KRAL, A
    YEGER, H
    LEWIS, WH
    JONES, C
    HOUSMAN, DE
    [J]. CELL, 1990, 60 (03) : 509 - 520
  • [4] Culling C. F. A., 1985, CELLULAR PATHOLOGY T, V4th
  • [5] DALE L, 1992, DEVELOPMENT, V115, P573
  • [6] THE HOX-4.8 GENE IS LOCALIZED AT THE 5' EXTREMITY OF THE HOX-4 COMPLEX AND IS EXPRESSED IN THE MOST POSTERIOR PARTS OF THE BODY DURING DEVELOPMENT
    DOLLE, P
    IZPISUABELMONTE, JC
    BONCINELLI, E
    DUBOULE, D
    [J]. MECHANISMS OF DEVELOPMENT, 1991, 36 (1-2) : 3 - 13
  • [7] DEREGULATION OF PAX-2 EXPRESSION IN TRANSGENIC MICE GENERATES SEVERE KIDNEY ABNORMALITIES
    DRESSLER, GR
    WILKINSON, JE
    ROTHENPIELER, UW
    PATTERSON, LT
    WILLIAMSSIMONS, L
    WESTPHAL, H
    [J]. NATURE, 1993, 362 (6415) : 65 - 67
  • [8] DRESSLER GR, 1990, DEVELOPMENT, V109, P787
  • [9] FAWCETT D, 1995, DEVELOPMENT, V121, P671
  • [10] DECAPENTAPLEGIC ACTS AS A MORPHOGEN TO ORGANIZE DORSAL-VENTRAL PATTERN IN THE DROSOPHILA EMBRYO
    FERGUSON, EL
    ANDERSON, KV
    [J]. CELL, 1992, 71 (03) : 451 - 461