Sox8 is a specific marker for muscle satellite cells and inhibits myogenesis

被引:79
作者
Schmidt, K
Glaser, G
Wernig, A
Wegner, M
Rosorius, O
机构
[1] Univ Erlangen Nurnberg, Inst Biochem, D-91054 Erlangen, Germany
[2] Univ Bonn, Inst Physiol & Neurophysiol, D-53111 Bonn, Germany
关键词
D O I
10.1074/jbc.M301539200
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
Sox8 belongs to a family of transcription regulators characterized by a unique DNA-binding domain known as the high mobility group box. Many Sox proteins play fundamental roles in vertebrate development and differentiation processes. Expression of Sox8 is strong during embryonic muscle development and gradually declines postnatally. In this study, we report that in adult skeletal muscle Sox8 is confined to satellite cells. Downregulation during myogenic differentiation was also detected in cell culture systems and occurred in parallel with down-regulation of the related Sox9. Overexpression of Sox8 or Sox9 on the other hand disrupted myoblasts in their ability to form myotubes. Concomitantly, expression of MyoD and myogenin decreased and basal as well as MyoD-induced activities of the myogenin promoter were strongly reduced in a Sox8-dependent manner. Our data suggest that Sox8 acts as a specific negative regulator of skeletal muscle differentiation, possibly by interfering with the function of myogenic basic helix-loop-helix proteins.
引用
收藏
页码:29769 / 29775
页数:7
相关论文
共 37 条
[1]  
[Anonymous], 1994, MANIPULATING MOUSE E
[2]   Expression of CD34 and Myf5 defines the majority of quiescent adult skeletal muscle satellite cells [J].
Beauchamp, JR ;
Heslop, L ;
Yu, DSW ;
Tajbakhsh, S ;
Kelly, RG ;
Wernig, A ;
Buckingham, ME ;
Partridge, TA ;
Zammit, PS .
JOURNAL OF CELL BIOLOGY, 2000, 151 (06) :1221-1233
[3]   Dynamics of myoblast transplantation reveal a discrete minority of precursors with stem cell-like properties as the myogenic source [J].
Beauchamp, JR ;
Morgan, JE ;
Pagel, CN ;
Partridge, TA .
JOURNAL OF CELL BIOLOGY, 1999, 144 (06) :1113-1121
[4]   Muscle differentiation is antagonized by SOX15, a new member of the SOX protein family [J].
Béranger, F ;
Méjean, C ;
Moniot, B ;
Berta, P ;
Vandromme, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (21) :16103-16109
[5]   Sox9 is required for cartilage formation [J].
Bi, WM ;
Deng, JM ;
Zhang, ZP ;
Behringer, RR ;
de Crombrugghe, B .
NATURE GENETICS, 1999, 22 (01) :85-89
[6]   The transcription factor Sox10 is a key regulator of peripheral glial development [J].
Britsch, S ;
Goerich, DE ;
Riethmacher, D ;
Peirano, RI ;
Rossner, M ;
Nave, KA ;
Birchmeier, C ;
Wegner, M .
GENES & DEVELOPMENT, 2001, 15 (01) :66-78
[7]   CAMPOMELIC DYSPLASIA AND AUTOSOMAL SEX REVERSAL CAUSED BY MUTATIONS IN AN SRY-RELATED GENE [J].
FOSTER, JW ;
DOMINGUEZSTEGLICH, MA ;
GUIOLI, S ;
KWOK, C ;
WELLER, PA ;
STEVANOVIC, M ;
WEISSENBACH, J ;
MANSOUR, S ;
YOUNG, ID ;
GOODFELLOW, PN ;
BROOK, JD ;
SCHAFER, AJ .
NATURE, 1994, 372 (6506) :525-530
[8]   A nuclear export signal within the high mobility group domain regulates the nucleocytoplasmic translocation of SOX9 during sexual determination [J].
Gasca, S ;
Cañizares, J ;
Santa Barbara, P ;
Méjean, C ;
Poulat, F ;
Berta, P ;
Boizet-Bonhoure, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (17) :11199-11204
[9]   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
[10]   EXPRESSION PATTERN OF M-CADHERIN IN NORMAL, DENERVATED, AND REGENERATING MOUSE MUSCLES [J].
IRINTCHEV, A ;
ZESCHNIGK, M ;
STARZINSKIPOWITZ, A ;
WERNIG, A .
DEVELOPMENTAL DYNAMICS, 1994, 199 (04) :326-337