A microarray analysis of the XX Wnt4 mutant gonad targeted at the identification of genes involved in testis vascular differentiation

被引:17
作者
Coveney, Douglas [1 ]
Ross, Andrea J. [1 ]
Slone, Jesse D. [1 ]
Capel, Blanche [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
关键词
sex determination/differentiation; microarray; Wnt4; testis; ovary;
D O I
10.1016/j.modgep.2006.05.012
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
One of the earliest morphological changes during testicular differentiation is the establishment of an XY specific vasculature. The testis vascular system is derived from mesonephric endothelial cells that migrate into the gonad. In the XX gonad, mesonephric cell migration and testis vascular development are inhibited by WNT4 signaling. In Wnt4 mutant XX gonads, endothelial cells migrate from the mesonephros and form a male-like coelomic vessel. Interestingly, this process occurs in the absence of other obvious features of testis differentiation, suggesting that Wnt4 specifically inhibits XY vascular development. Consequently, the XX Wnt4 mutant mice presented an opportunity to focus a gene expression screen on the processes of mesonephric cell migration and testicular vascular development. We compared differences in gene expression between XY Wnt4+/+ and XX Wnt4+/+ gonads and between XX Wnt4+/+ and XX Wnt4+/+ gonads to identify sets of genes similarly upregulated in wildtype XY gonads and XX mutant gonads or upregulated in XX gonads as compared to XY gonads and XX mutant gonads. We show that several genes identified in the first set are expressed in vascular domains, and have predicted functions related to cell migration or vascular development. However, the expression patterns and known functions of other genes are not consistent with roles in these processes. This screen has identified candidates for regulation of sex specific vascular development, and has implicated a role for WNT4 signaling in the development of Sertoli and germ cell lineages not immediately obvious from previous phenotypic analyses. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:82 / 92
页数:11
相关论文
共 97 条
[11]   Pdgfr-α mediates testis cord organization and fetal Leydig cell development in the XY gonad [J].
Brennan, J ;
Tilmann, C ;
Capel, B .
GENES & DEVELOPMENT, 2003, 17 (06) :800-810
[12]   Divergent vascular mechanisms downstream of Sry establish the arterial system in the XY gonad [J].
Brennan, J ;
Karl, J ;
Capel, B .
DEVELOPMENTAL BIOLOGY, 2002, 244 (02) :418-428
[13]  
BUEHR M, 1993, DEVELOPMENT, V117, P273
[14]   Extensive vascularization of developing mouse ovaries revealed by caveolin-1 expression [J].
Bullejos, M ;
Bowles, J ;
Koopman, P .
DEVELOPMENTAL DYNAMICS, 2002, 225 (01) :95-99
[15]   Mice deficient in the candidate tumor suppressor gene Hic1 exhibit developmental defects of structures affected in the Miller-Dieker syndrome [J].
Carter, MG ;
Johns, MA ;
Zeng, XB ;
Zhou, L ;
Zink, MC ;
Mankowski, JL ;
Donovan, DM ;
Baylin, SB .
HUMAN MOLECULAR GENETICS, 2000, 9 (03) :413-419
[16]   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
[17]   Heterozygous disruption of Hic1 predisposes mice to a gender-dependent spectrum of malignant tumors [J].
Chen, WY ;
Zeng, XB ;
Carter, MG ;
Morrell, CN ;
Yen, RWC ;
Esteller, M ;
Watkins, DN ;
Herman, JG ;
Mankowski, JL ;
Baylin, SB .
NATURE GENETICS, 2003, 33 (02) :197-202
[18]   Male-to-female sex reversal in mice lacking fibroblast growth factor 9 [J].
Colvin, JS ;
Green, RP ;
Schmahl, J ;
Capel, B ;
Ornitz, DM .
CELL, 2001, 104 (06) :875-889
[19]   Disrupted gonadogenesis and male-to-female sex reversal in Pod1 knockout mice [J].
Cui, SY ;
Ross, A ;
Stallings, N ;
Parker, KL ;
Capel, B ;
Quaggin, SE .
DEVELOPMENT, 2004, 131 (16) :4095-4105
[20]   Simpson Golabi Behmel syndrome: Progress toward understanding the molecular basis for overgrowth, malformation, and cancer predisposition [J].
DeBaun, MR ;
Ess, J ;
Saunders, S .
MOLECULAR GENETICS AND METABOLISM, 2001, 72 (04) :279-286