Acquisition of SOX transcription factor specificity through protein-protein interaction, modulation of Wnt signalling and post-translational modification

被引:74
作者
Bernard, Pascal [1 ]
Harley, Vincent R. [1 ]
机构
[1] Monash Med Ctr, Prince Henrys Inst Med Res, Clayton, Vic 3168, Australia
基金
英国医学研究理事会;
关键词
SOX; Protein interaction; Transcription; Wnt signalling; Post-translational modification; TESTIS-DETERMINING FACTOR; DETERMINING FACTOR SRY; II COLLAGEN GENE; DNA-BINDING; BETA-CATENIN; CELL-DIFFERENTIATION; SEX DETERMINATION; HMG BOX; CHROMOSOMAL-PROTEINS; PHYSICALLY INTERACT;
D O I
10.1016/j.biocel.2009.10.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
SOX transcription factors contain a high mobility group (HMG) box that confers sequence-specific (in the case of SOX/TCF) DNA binding ability to the protein. SOX proteins are transcriptional regulators involved in diverse tissues and developmental processes. Based on protein sequence comparisons, the SOX family is divided into eight groups. SOX proteins belonging to the same group tend to have overlapping tissue expression profiles and are able to functionally substitute for one another. However. SOX proteins belonging to different groups often do not show redundant regulatory functions. To achieve their specific actions, SOX proteins rely on interactions with a wide variety of proteins. The choice of binding partners as well as post-translational modifications of SOX proteins confers target gene specificity to the HMG box proteins which otherwise have weak DNA binding specificity. SOX proteins also regulate signalling pathways, such as the Wnt pathway by interacting with p-catenin and/or TCF/LEF transcription factors, employing different mechanisms to achieve similar functional outcomes. Here we review extensively the SOX protein interactions with partner co-factors, the ability of SOX proteins to modulate Wnt signalling and the effect of post-translational modification of SOX proteins on their function. Crown Copyright (C) 2009 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:400 / 410
页数:11
相关论文
共 118 条
  • [1] The transcription factor Sox9 is degraded by the ubiquitin-proteasome system and stabilized by a mutation in a ubiquitin-target site
    Akiyama, H
    Kamitani, T
    Yang, XH
    Kandyil, R
    Bridgewater, LC
    Fellous, M
    Mori-Akiyama, Y
    de Crombrugghe, B
    [J]. MATRIX BIOLOGY, 2005, 23 (08) : 499 - 505
  • [2] Interactions between Sox9 and β-catenin control chondrocyte differentiation
    Akiyama, H
    Lyons, JP
    Mori-Akiyama, Y
    Yang, XH
    Zhang, R
    Zhang, ZP
    Deng, JM
    Taketo, MM
    Nakamura, T
    Behringer, RR
    McCrea, PD
    de Crombrugghe, B
    [J]. GENES & DEVELOPMENT, 2004, 18 (09) : 1072 - 1087
  • [3] Synergistic activation of the fibroblast growth factor 4 enhancer by Sox2 and Oct-3 depends on protein-protein interactions facilitated by a specific spatial arrangement of factor binding sites
    Ambrosetti, DC
    Basilico, C
    Dailey, L
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (11) : 6321 - 6329
  • [4] Targeted mutagenesis of the endogenous mouse Mis gene promoter:: In vivo definition of genetic pathways of vertebrate sexual development
    Arango, NA
    Lovell-Badge, R
    Behringer, RR
    [J]. CELL, 1999, 99 (04) : 409 - 419
  • [5] Multipotent cell lineages in early mouse development depend on SOX2 function
    Avilion, AA
    Nicolis, SK
    Pevny, LH
    Perez, L
    Vivian, N
    Lovell-Badge, R
    [J]. GENES & DEVELOPMENT, 2003, 17 (01) : 126 - 140
  • [6] BAGHERIFAM S, 2009, INT J BIOCH CELL BIO
  • [7] A Positive Regulatory Role for the mSin3A-HDAC Complex in Pluripotency through Nanog and Sox2
    Baltus, Gretchen A.
    Kowalski, Michael P.
    Tutter, Antonin V.
    Kadam, Shilpa
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (11) : 6998 - 7006
  • [8] Sox9 regulates cell proliferation and is required for Paneth cell differentiation in the intestinal epithelium
    Bastide, Pauline
    Darido, Charbel
    Pannequiri, Julie
    Kist, Ralf
    Robine, Sylvie
    Marty-Double, Christiane
    Bibeau, Frederic
    Scherer, Gerd
    Joubert, Dominique
    Hollande, Frederic
    Blache, Philippe
    Jay, Philippe
    [J]. JOURNAL OF CELL BIOLOGY, 2007, 178 (04) : 635 - 648
  • [9] A post-translational modification code for transcription factors: sorting through a sea of signals
    Benayoun, Berenice A.
    Veitia, Reiner A.
    [J]. TRENDS IN CELL BIOLOGY, 2009, 19 (05) : 189 - 197
  • [10] Dimerization of SOX9 is required for chondrogenesis, but not for sex determination
    Bernard, P
    Tang, PY
    Dewing, P
    Harley, VR
    Vilain, E
    [J]. HUMAN MOLECULAR GENETICS, 2003, 12 (14) : 1755 - 1765