TY - JOUR
T1 - Identification of the genes regulated by Wnt-4, a critical signal for commitment of the ovary
AU - Naillat, Florence
AU - Yan, Wenying
AU - Karjalainen, Riikka
AU - Liakhovitskaia, Anna
AU - Samoylenko, Anatoly
AU - Xu, Qi
AU - Sun, Zhandong
AU - Shen, Bairong
AU - Medvinsky, Alexander
AU - Quaggin, Susan
AU - Vainio, Seppo J.
PY - 2015/1/1
Y1 - 2015/1/1
N2 - The indifferent mammalian embryonic gonad generates an ovary or testis, but the factors involved are still poorly known. The Wnt-4 signal represents one critical female determinant, since its absence leads to partial female-to-male sex reversal in mouse, but its signalling is as well implicated in the testis development. We used the Wnt-4 deficient mouse as a model to identify candidate gonadogenesis genes, and found that the Notum, Phlda2, Runx-1 and Msx1 genes are typical of the wild-type ovary and the Osr2, Dach2, Pitx2 and Tacr3 genes of the testis. Strikingly, the expression of these latter genes becomes reversed in the Wnt-4 knock-out ovary, suggesting a role in ovarian development. We identified the transcription factor Runx-1 as a Wnt-4 signalling target gene, since it is expressed in the ovary and is reduced upon Wnt-4 knock-out. Consistent with this, introduction of the Wnt-4 signal into early ovary cells ex vivo induces Runx-1 expression, while conversely Wnt-4 expression is down-regulated in the absence of Runx-1. We conclude that the Runx-1 gene can be a Wnt-4 signalling target, and that Runx-1 and Wnt-4 are mutually interdependent in their expression. The changes in gene expression due to the absence of Wnt-4 in gonads reflect the sexually dimorphic role of this signal and its complex gene network in mammalian gonad development.
AB - The indifferent mammalian embryonic gonad generates an ovary or testis, but the factors involved are still poorly known. The Wnt-4 signal represents one critical female determinant, since its absence leads to partial female-to-male sex reversal in mouse, but its signalling is as well implicated in the testis development. We used the Wnt-4 deficient mouse as a model to identify candidate gonadogenesis genes, and found that the Notum, Phlda2, Runx-1 and Msx1 genes are typical of the wild-type ovary and the Osr2, Dach2, Pitx2 and Tacr3 genes of the testis. Strikingly, the expression of these latter genes becomes reversed in the Wnt-4 knock-out ovary, suggesting a role in ovarian development. We identified the transcription factor Runx-1 as a Wnt-4 signalling target gene, since it is expressed in the ovary and is reduced upon Wnt-4 knock-out. Consistent with this, introduction of the Wnt-4 signal into early ovary cells ex vivo induces Runx-1 expression, while conversely Wnt-4 expression is down-regulated in the absence of Runx-1. We conclude that the Runx-1 gene can be a Wnt-4 signalling target, and that Runx-1 and Wnt-4 are mutually interdependent in their expression. The changes in gene expression due to the absence of Wnt-4 in gonads reflect the sexually dimorphic role of this signal and its complex gene network in mammalian gonad development.
KW - Female development
KW - Germ line
KW - Organogenesis
KW - Ovary
KW - Runx-1
KW - Sex determination
KW - Somatic cells
KW - Testis
KW - Wnt-4
UR - http://www.scopus.com/inward/record.url?scp=84924363333&partnerID=8YFLogxK
U2 - 10.1016/j.yexcr.2015.01.010
DO - 10.1016/j.yexcr.2015.01.010
M3 - Article
C2 - 25645944
AN - SCOPUS:84924363333
SN - 0014-4827
VL - 332
SP - 163
EP - 178
JO - Experimental Cell Research
JF - Experimental Cell Research
IS - 2
ER -