SOX E genes: SOX9 and SOX8 in mammalian testis development

被引:118
作者
Barrionuevo, Francisco [1 ]
Scherer, Gerd [1 ]
机构
[1] Univ Freiburg, Inst Human Genet, D-79106 Freiburg, Germany
关键词
SOX8; SOX9; SOX10; Testis; Sertoli cell; AUTOSOMAL SEX REVERSAL; SRY-RELATED GENE; CAMPOMELIC DYSPLASIA; TRANSCRIPTION FACTOR; SERTOLI-CELLS; IN-VIVO; DIFFERENTIATION; MOUSE; MICE; TRANSACTIVATION;
D O I
10.1016/j.biocel.2009.07.015
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
The group E SOX proteins consist of SOX8. SOX9 and SOX10. These transcription factors contain, besides a DNA-binding HMG domain and a transactivation domain, a DNA-dependent dimerization domain, unique among SOX proteins. Among these three SOX E proteins, which are all expressed during mammalian testis development, SOX9 stands out in importance. It is SOX9 that becomes activated by SRY in pre-Sertoli cells, executing SRY's role as a testis-determining factor by inducing Sertoli cell and testis cord differentiation. However, Sox9 is dispensable during subsequent embryonic and postnatal testis development, since ablation of Sox9 at embryonic day 14.0, after the sex determination stage, only leads to late-onset sterility at about 5 months. A similar late male sterility phenotype occurs in constitutive Sox8 null mutants. In the combined absence of Sox9 and Sox8, primary male infertility evolves, revealing functional redundancy. Loss of Sox10 has no effect on testis development. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:433 / 436
页数:4
相关论文
共 34 条
[1]   Interactions between Sox9 and β-catenin control chondrocyte differentiation [J].
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 .
GENES & DEVELOPMENT, 2004, 18 (09) :1072-1087
[2]   Targeted mutagenesis of the endogenous mouse Mis gene promoter:: In vivo definition of genetic pathways of vertebrate sexual development [J].
Arango, NA ;
Lovell-Badge, R ;
Behringer, RR .
CELL, 1999, 99 (04) :409-419
[3]   Homozygous inactivation of Sox9 causes complete XY sex reversal in mice [J].
Barrionuevo, F ;
Bagheri-Fam, S ;
Klattig, J ;
Kist, R ;
Taketo, MM ;
Englert, C ;
Scherer, G .
BIOLOGY OF REPRODUCTION, 2006, 74 (01) :195-201
[4]   Testis cord differentiation after the sex determination stage is independent of Sox9 but fails in the combined absence of Sox9 and Sox8 [J].
Barrionuevo, Francisco ;
Georg, Ina ;
Scherthan, Harry ;
Lecureuil, Charlotte ;
Guillou, Florian ;
Wegner, Michael ;
Scherer, Gerd .
DEVELOPMENTAL BIOLOGY, 2009, 327 (02) :301-312
[5]   Dimerization of SOX9 is required for chondrogenesis, but not for sex determination [J].
Bernard, P ;
Tang, PY ;
Dewing, P ;
Harley, VR ;
Vilain, E .
HUMAN MOLECULAR GENETICS, 2003, 12 (14) :1755-1765
[6]   The Cerebellin 4 Precursor Gene Is a Direct Target of SRY and SOX9 in Mice [J].
Bradford, Stephen T. ;
Hiramatsu, Ryuji ;
Maddugoda, Madhavi P. ;
Bernard, Pascal ;
Chaboissier, Marie-Christine ;
Sinclair, Andrew ;
Schedl, Andreas ;
Harley, Vincent ;
Kanai, Yoshiakira ;
Koopman, Peter ;
Wilhelm, Dagmar .
BIOLOGY OF REPRODUCTION, 2009, 80 (06) :1178-1188
[7]   Functional analysis of Sox8 and Sox9 during sex determination in the mouse [J].
Chaboissier, MC ;
Kobayashi, A ;
Vidal, VIP ;
Lützkendorf, S ;
van de Kant, HJG ;
Wegner, M ;
de Rooij, DG ;
Behringer, RR ;
Schedl, A .
DEVELOPMENT, 2004, 131 (09) :1891-1901
[8]   Wt1 negatively regulates β-catenin signaling during testis development [J].
Chang, Hao ;
Gao, Fei ;
Guillou, Florian ;
Taketo, Makoto M. ;
Huff, Vicki ;
Behringer, Richard R. .
DEVELOPMENT, 2008, 135 (10) :1875-1885
[9]   Presumptive pre-Sertoli cells express genes involved in cell proliferation and cell signalling during a critical window in early testis differentiation [J].
Cory, Aron T. ;
Boyer, Alexandre ;
Pilon, Nicolas ;
Lussier, Jacques G. ;
Silversides, David W. .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 2007, 74 (12) :1491-1504
[10]   Direct interaction of SRY-related protein SOX9 and steroidogenic factor 1 regulates transcription of the human anti-Mullerian hormone gene [J].
De Santa Barbara, P ;
Bonneaud, N ;
Boizet, B ;
Desclozeaux, M ;
Moniot, B ;
Sudbeck, P ;
Scherer, G ;
Poulat, F ;
Berta, P .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (11) :6653-6665