Finding Partners: How BMPs Select Their Targets

被引:38
作者
Blitz, Ira L. [1 ]
Cho, Ken W. Y.
机构
[1] Univ Calif Irvine, Dept Dev & Cell Biol, Irvine, CA 92697 USA
关键词
TGF beta signaling; Xenopus; Drosophila; D-V patterning; Smad; Schnurri; ZINC-FINGER PROTEIN; MAJOR HISTOCOMPATIBILITY COMPLEX; SCHNURRI HOMOLOG SMA-9; DPP MORPHOGEN GRADIENT; TGF-BETA SIGNALS; DNA-BINDING; TRANSCRIPTIONAL REPRESSOR; BONE-FORMATION; FUNCTIONAL-CHARACTERIZATION; RESPONSIVE SILENCERS;
D O I
10.1002/dvdy.21984
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
The bone morphogenetic protein (BMP) signaling pathway is a conserved and evolutionarily ancient regulatory module affecting a large variety of cellular behaviors. The evolutionary flexibility in using BMP responses presumably arose by co-option of a canonical BMP signaling cascade to regulate the transcription of diverse batteries of target genes. This begs the question of how seemingly interchangeable BMP signaling components elicit widely different outputs in different cell types, an important issue in the context of understanding how BMP signaling integrates with gene regulatory networks to control development. Because a molecular understanding of how BMP signaling activates different batteries of target genes is an essential prerequisite to comprehending the roles of BMPs in regulating cellular responses, here we review the current knowledge of how BMP-regulated target genes are selected by the signal transduction machinery. We highlight recent studies suggesting the evolutionary conservation of BMP target gene regulation signaling by Schnurri family zinc finger proteins. Developmental Dynamics 238:1321-1331, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:1321 / 1331
页数:11
相关论文
共 104 条
[1]   Wnt and TGF-β Expression in the Sponge Amphimedon queenslandica and the Origin of Metazoan Embryonic Patterning [J].
Adamska, Maja ;
Degnan, Sandie M. ;
Green, Kathryn M. ;
Adamski, Marcin ;
Craigie, Alina ;
Larroux, Claire ;
Degnan, Bernard M. .
PLOS ONE, 2007, 2 (10)
[2]   Dose-dependent Smad1, Smad5 and Smad8 signaling in the early mouse embryo [J].
Arnold, Sebastian J. ;
Maretto, Silvia ;
Islam, Ayesha ;
Bikoff, Elizabeth K. ;
Robertson, Elizabeth J. .
DEVELOPMENTAL BIOLOGY, 2006, 296 (01) :104-118
[3]   THE DROSOPHILA SCHNURRI GENE ACTS IN THE DPP/TGF-BETA SIGNALING PATHWAY AND ENCODES A TRANSCRIPTION FACTOR HOMOLOGOUS TO THE HUMAN MBP FAMILY [J].
ARORA, K ;
DAI, H ;
KAZUKO, SG ;
JAMAL, J ;
OCONNOR, MB ;
LETSOU, A ;
WARRIOR, R .
CELL, 1995, 81 (05) :781-790
[4]   A LARGE PROTEIN CONTAINING ZINC FINGER DOMAINS BINDS TO RELATED SEQUENCE ELEMENTS IN THE ENHANCERS OF THE CLASS-I MAJOR HISTOCOMPATIBILITY COMPLEX AND KAPPA-IMMUNOGLOBULIN GENES [J].
BALDWIN, AS ;
LECLAIR, KP ;
SINGH, H ;
SHARP, PA .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (04) :1406-1414
[5]   GATA- and Smad1-dependent enhancers in the Smad7 gene differentially interpret bone morphogenetic protein concentrations [J].
Benchabane, H ;
Wrana, JL .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (18) :6646-6661
[6]   Genetic screen for regulators of ind expression identifies shrew as encoding a novel twisted gastrulation-like protein involved in dpp signaling [J].
Bonds, Morgan ;
Sands, Jennifer ;
Poulson, Will ;
Harvey, Canda ;
Von Ohlen, Tonia .
DEVELOPMENTAL DYNAMICS, 2007, 236 (12) :3524-3531
[7]   The cardiac determination factor, Nkx2-5, is activated by mutual cofactors GATA-4 and Smad1/4 via a novel upstream enhancer [J].
Brown, CO ;
Chi, X ;
Garcia-Gras, E ;
Shirai, M ;
Feng, XH ;
Schwartz, RJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (11) :10659-10669
[8]   Transducing the Dpp morphogen gradient in the wing of Drosophila:: Regulation of Dpp targets by brinker [J].
Campbell, G ;
Tomlinson, A .
CELL, 1999, 96 (04) :553-562
[9]  
Candia AF, 1997, DEVELOPMENT, V124, P4467
[10]   The L3 loop and C-terminal phosphorylation jointly define Smad protein trimerization [J].
Chacko, BM ;
Qin, B ;
Correia, JJ ;
Lam, SS ;
de Caestecker, MP ;
Lin, K .
NATURE STRUCTURAL BIOLOGY, 2001, 8 (03) :248-253