Smad transcription factors

被引:1951
作者
Massagué, J
Seoane, J
Wotton, D
机构
[1] Mem Sloan Kettering Canc Ctr, Howard Hughes Med Inst, Canc Biol & Genet Program, New York, NY 10021 USA
[2] Valle Hebron Univ Hosp, Res Inst, Med Oncol Res Program, ICREA, Barcelona 08035, Spain
[3] Univ Virginia, Ctr Cell Signaling, Dept Biochem & Mol Genet, Charlottesville, VA 22908 USA
关键词
D O I
10.1101/gad.1350705
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Smad transcription factors lie at the core of one of the most versatile cytokine signaling pathways in metazoan biology-the transforming growth factor-beta (TGF beta) pathway. Recent progress has shed light into the processes of Smad activation and deactivation, nucleocytoplasmic dynamics, and assembly of transcriptional complexes. A rich repertoire of regulatory devices exerts control over each step of the Smad pathway. This knowledge is enabling work on more complex questions about the organization, integration, and modulation of Smad-dependent transcriptional programs. We are beginning to uncover self-enabled gene response cascades, graded Smad response mechanisms, and Smad-dependent synexpression groups. Our growing understanding of TGF beta signaling through the Smad pathway provides general principles for how animal cells translate complex inputs into concrete behavior.
引用
收藏
页码:2783 / 2810
页数:28
相关论文
共 256 条
  • [71] Hayes SA, 2001, CANCER RES, V61, P2112
  • [72] Mouse models of holoprosencephaly
    Hayhurst, M
    McConnell, SK
    [J]. CURRENT OPINION IN NEUROLOGY, 2003, 16 (02) : 135 - 141
  • [73] The transforming activity of ski and SnoN is dependent on their ability to repress the activity of Smad proteins
    He, J
    Tegen, SB
    Krawitz, AR
    Martin, GS
    Luo, KX
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (33) : 30540 - 30547
  • [74] Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis
    Hellemans, J
    Preobrazhenska, O
    Willaert, A
    Debeer, P
    Verdonk, PCM
    Costa, T
    Janssens, K
    Menten, B
    Van Roy, N
    Vermeulen, SJT
    Savarirayan, R
    Van Hul, W
    Vanhoenacker, F
    Huylebroeck, D
    De Paepe, A
    Naeyaert, JM
    Vandesompele, J
    Speleman, F
    Verschueren, K
    Coucke, PJ
    Mortier, GR
    [J]. NATURE GENETICS, 2004, 36 (11) : 1213 - 1218
  • [75] Postgastrulation Smad2-deficient embryos show defects in embryo turning and anterior morphogenesis
    Heyer, J
    Escalante-Alcalde, D
    Lia, M
    Boettinger, E
    Edelmann, W
    Stewart, CL
    Kucherlapati, R
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (22) : 12595 - 12600
  • [76] The adaptor molecule Disabled-2 links the transforming growth factor β receptors to the Smad pathway
    Hocevar, BA
    Smine, A
    Xu, XX
    Howe, PH
    [J]. EMBO JOURNAL, 2001, 20 (11) : 2789 - 2801
  • [77] Bone morphogenetic proteins: Multifunctional regulators of vertebrate development
    Hogan, BLM
    [J]. GENES & DEVELOPMENT, 1996, 10 (13) : 1580 - 1594
  • [78] MADR1, a MAD-related protein that functions in BMP2 signaling pathways
    Hoodless, PA
    Haerry, T
    Abdollah, S
    Stapleton, M
    OConnor, MB
    Attisano, L
    Wrana, JL
    [J]. CELL, 1996, 85 (04) : 489 - 500
  • [79] Smad1, β-catenin and Tcf4 associate in a molecular complex with the Myc promoter in dysplastic renal tissue and cooperate to control Myc transcription
    Hu, MC
    Rosenblum, ND
    [J]. DEVELOPMENT, 2005, 132 (01): : 215 - 225
  • [80] Synergism between transcription factors TFE3 and Smad3 in transforming growth factor-β-induced transcription of the Smad7 gene
    Hua, XX
    Miller, ZA
    Benchabane, H
    Wrana, JL
    Lodish, HF
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (43) : 33205 - 33208