Secrets to a healthy Sox life: lessons for melanocytes

被引:86
作者
Wegner, M [1 ]
机构
[1] Univ Erlangen Nurnberg, Inst Biochem, D-91054 Erlangen, Germany
来源
PIGMENT CELL RESEARCH | 2005年 / 18卷 / 02期
关键词
Sry; high-mobility-group; bending; transcription factor; co-activator; Mitf;
D O I
10.1111/j.1600-0749.2005.00218.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Sox proteins are transcriptional regulators with a high-mobility-group domain as sequence-specific DNA-binding domain. For function, they generally require other transcription factors as partner proteins. Sox proteins furthermore affect DNA topology and may shape the conformation of enhancer-bound multiprotein complexes as architectural proteins. Recent studies suggest that Sox proteins are tightly regulated in their expression by many signalling pathways, and that their transcriptional activity is subject to post-translational modification and sequestration mechanisms. Sox proteins are thus ideally suited to perform their many different functions as transcriptional regulators throughout mammalian development. Their unique properties also cause Sox proteins to escape detection in many standard transcription assays. In melanocytes, studies have so far focused on the Sox10 protein which functions both during melanocyte specification and at later times in the melanocyte lineage. During specification, Sox10 activates the Mitf gene as the key regulator of melanocyte development. At later stages, it ensures cell-type specific expression of melanocyte genes such as Dopachrome tautomerase. Both activities require cooperation with transcriptional partner proteins such as Pax-3, CREB and eventually Mitf. If predictions can be made from other cell lineages, further functions of Sox proteins in melanocytes may still lie ahead.
引用
收藏
页码:74 / 85
页数:12
相关论文
共 126 条
[41]   Mutation of the Sry-related Sox10 gene in Dominant megacolon, a mouse model for human Hirschsprung disease [J].
Herbarth, B ;
Pingault, V ;
Bondurand, N ;
Kuhlbrodt, K ;
Hermans-Borgmeyer, I ;
Puliti, A ;
Lemort, N ;
Goossens, M ;
Wegner, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (09) :5161-5165
[42]   Sox10 is required for the early development of the prospective neural crest in Xenopus embryos [J].
Honoré, SM ;
Aybar, MJ ;
Mayor, R .
DEVELOPMENTAL BIOLOGY, 2003, 260 (01) :79-96
[43]   Complementation of melanocyte development in SOX10 mutant neural crest using lineage-directed gene transfer [J].
Hou, L ;
Loftus, SK ;
Incao, A ;
Chen, A ;
Pavan, WJ .
DEVELOPMENTAL DYNAMICS, 2004, 229 (01) :54-62
[44]   Phosphorylation of SOX9 by cyclic AMP-Dependent protein kinase a enhances SOX9's ability to transactivate a col2a1 chondrocyte-specific enhancer [J].
Huang, WD ;
Zhou, X ;
Lefebvre, V ;
De Crombrugghe, B .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (11) :4149-4158
[45]   A new long form of c-Maf cooperates with Sox9 to activate the type II collagen gene [J].
Huang, WD ;
Lu, N ;
Eberspaecher, H ;
de Crombrugghe, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (52) :50668-50675
[46]   The chondrogenic transcription factor Sox9 is a target of signaling by the parathyroid hormone-related peptide in the growth plate of endochondral bones [J].
Huang, WD ;
Chung, U ;
Kronenberg, HM ;
de Crombrugghe, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (01) :160-165
[47]   A tissue-restricted cAMP transcriptional response -: SOX10 modulates α-melanocyte-stimulating hormone-triggered expression of microphthalmia-associated transcription factor in melanocytes [J].
Huber, WE ;
Price, ER ;
Widlund, HR ;
Du, JY ;
Davis, IJ ;
Wegner, M ;
Fisher, DE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (46) :45224-45230
[48]   Functional identification of the pro-apoptotic effector domain in human Sox4 [J].
Hur, EH ;
Hur, W ;
Choi, JY ;
Kim, IK ;
Kim, HY ;
Yoon, SK ;
Rhim, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 325 (01) :59-67
[49]   Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations [J].
Inoue, K ;
Khajavi, M ;
Ohyama, T ;
Hirabayashi, S ;
Wilson, J ;
Reggin, JD ;
Mancias, P ;
Butler, IJ ;
Wilkinson, MF ;
Wegner, M ;
Lupski, JR .
NATURE GENETICS, 2004, 36 (04) :361-369
[50]   Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia [J].
Irrthum, A ;
Devriendt, K ;
Chitayat, D ;
Matthijs, G ;
Glade, C ;
Steijlen, PM ;
Fryns, JP ;
Van Steensel, MAM ;
Vikkula, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (06) :1470-1478