Genetic analysis of the roles of BMP2, BMP4, and BMP7 in limb patterning and skeletogenesis

被引:435
作者
Bandyopadhyay, Amitabha
Tsuji, Kunikazu
Cox, Karen
Harfe, Brian D.
Rosen, Vicki
Tabin, Clifford J. [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Genet, Boston, MA USA
[2] Harvard Univ, Sch Dent Med, Dept Dev Biol, Boston, MA 02115 USA
[3] Univ Florida, Dept Mol Genet & Microbiol, Gainesville, FL USA
关键词
D O I
10.1371/journal.pgen.0020216
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Bone morphogenetic protein (BMP) family members, including BMP2, BMP4, and BMP7, are expressed throughout limb development. BMPs have been implicated in early limb patterning as well as in the process of skeletogenesis. However, due to complications associated with early embryonic lethality, particularly for Bmp2 and Bmp4, and with functional redundancy among BMP molecules, it has been difficult to decipher the specific roles of these BMP molecules during different stages of limb development. To circumvent these issues, we have constructed a series of mouse strains lacking one or more of these BMPs, using conditional alleles in the case of Bmp2 and Bmp4 to remove them specifically from the limb bud mesenchyme. Contrary to earlier suggestions, our results indicate that BMPs neither act as secondary signals downstream of Sonic Hedghog (SHH) in patterning the anteroposterior axis nor as signals from the interdigital mesenchyme in specifying digit identity. We do find that a threshold level of BMP signaling is required for the onset of chondrogenesis, and hence some chondrogenic condensations fail to form in limbs deficient in both BMP2 and BMP4. However, in the condensations that do form, subsequent chondrogenic differentiation proceeds normally even in the absence of BMP2 and BMP7 or BMP2 and BMP4. In contrast, we find that the loss of both BMP2 and BMP4 results in a severe impairment of osteogenesis.
引用
收藏
页码:2116 / 2130
页数:15
相关论文
共 61 条
[1]   In vivo convergence of BMP and MAPK signaling pathways: impact of differential Smad1 phosphorylation on development and homeostasis [J].
Aubin, J ;
Davy, A ;
Soriano, P .
GENES & DEVELOPMENT, 2004, 18 (12) :1482-1494
[2]   NUCLEOTIDE-SEQUENCES OF COMPLEMENTARY DEOXYRIBONUCLEIC ACIDS FOR THE PRO-ALPHA-1 CHAIN OF HUMAN TYPE-I PROCOLLAGEN - STATISTICAL EVALUATION OF STRUCTURES THAT ARE CONSERVED DURING EVOLUTION [J].
BERNARD, MP ;
CHU, ML ;
MYERS, JC ;
RAMIREZ, F ;
EIKENBERRY, EF ;
PROCKOP, DJ .
BIOCHEMISTRY, 1983, 22 (22) :5213-5223
[3]   A somitic compartment of tendon progenitors [J].
Brent, AE ;
Schweitzer, R ;
Tabin, CJ .
CELL, 2003, 113 (02) :235-248
[4]   Control of vertebrate limb outgrowth by the proximal factor Meis2 and distal antagonism of BMPs by Gremlin [J].
Capdevila, J ;
Tsukui, T ;
Esteban, CR ;
Zappavigna, V ;
Belmonte, JCI .
MOLECULAR CELL, 1999, 4 (05) :839-849
[5]   Endogenous and ectopic expression of noggin suggests a conserved mechanism for regulation of BMP function during limb and somite patterning [J].
Capdevila, J ;
Johnson, RL .
DEVELOPMENTAL BIOLOGY, 1998, 197 (02) :205-217
[6]   Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function [J].
Chiang, C ;
Ying, LTT ;
Lee, E ;
Young, KE ;
Corden, JL ;
Westphal, H ;
Beachy, PA .
NATURE, 1996, 383 (6599) :407-413
[7]   Interdigital regulation of digit identity and homeotic transformation by modulated BMP signaling [J].
Dahn, RD ;
Fallon, JF .
SCIENCE, 2000, 289 (5478) :438-441
[8]  
Drossopoulou G, 2000, DEVELOPMENT, V127, P1337
[9]   Osf2/Cbfa1: A transcriptional activator of osteoblast differentiation [J].
Ducy, P ;
Zhang, R ;
Geoffroy, V ;
Ridall, AL ;
Karsenty, G .
CELL, 1997, 89 (05) :747-754
[10]   A REQUIREMENT FOR BONE MORPHOGENETIC PROTEIN-7 DURING DEVELOPMENT OF THE MAMMALIAN KIDNEY AND EYE [J].
DUDLEY, AT ;
LYONS, KM ;
ROBERTSON, EJ .
GENES & DEVELOPMENT, 1995, 9 (22) :2795-2807