spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

First published online 15 October 2003
doi: 10.1242/dev.00836


This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
dev.00836v1
130/24/5895    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Yao, H. H.-C.
Right arrow Articles by Capel, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Yao, H. H.-C.
Right arrow Articles by Capel, B.
Development 130, 5895-5902 (2003)
Copyright © 2003 The Company of Biologists Limited

Meiotic germ cells antagonize mesonephric cell migration and testis cord formation in mouse gonads

Humphrey H.-C. Yao*, Leo DiNapoli and Blanche Capel{dagger}

Department of Cell Biology, Duke University, Durham NC 27710, USA

{dagger} Author for correspondence (e-mail: b.capel{at}cellbio.duke.edu)

Accepted 14 August 2003

The developmental fate of primordial germ cells in the mammalian gonad depends on their environment. In the XY gonad, Sry induces a cascade of molecular and cellular events leading to the organization of testis cords. Germ cells are sequestered inside testis cords by 12.5 dpc where they arrest in mitosis. If the testis pathway is not initiated, germ cells spontaneously enter meiosis by 13.5 dpc, and the gonad follows the ovarian fate. We have previously shown that some testis-specific events, such as mesonephric cell migration, can be experimentally induced into XX gonads prior to 12.5 dpc. However, after that time, XX gonads are resistant to the induction of cell migration. In current experiments, we provide evidence that this effect is dependent on XX germ cells rather than on XX somatic cells. We show that, although mesonephric cell migration cannot be induced into normal XX gonads at 14.5 dpc, it can be induced into XX gonads depleted of germ cells. We also show that when 14.5 dpc XX somatic cells are recombined with XY somatic cells, testis cord structures form normally; however, when XX germ cells are recombined with XY somatic cells, cord structures are disrupted. Sandwich culture experiments suggest that the inhibitory effect of XX germ cells is mediated through short-range interactions rather than through a long-range diffusible factor. The developmental stage at which XX germ cells show a disruptive effect on the male pathway is the stage at which meiosis is normally initiated, based on the immunodetection of meiotic markers. We suggest that at the stage when germ cells commit to meiosis, they reinforce ovarian fate by antagonizing the testis pathway.

Key words: Primordial Germ cells, Meiosis, Sex Determination, Gonad, Testis, Sry




This article has been cited by other articles:


Home page
DevelopmentHome page
N. L. Manuylov, F. O. Smagulova, L. Leach, and S. G. Tevosian
Ovarian development in mice requires the GATA4-FOG2 transcription complex
Development, November 15, 2008; 135(22): 3731 - 3743.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
K. Tomizuka, K. Horikoshi, R. Kitada, Y. Sugawara, Y. Iba, A. Kojima, A. Yoshitome, K. Yamawaki, M. Amagai, A. Inoue, et al.
R-spondin1 plays an essential role in ovarian development through positively regulating Wnt-4 signaling
Hum. Mol. Genet., May 1, 2008; 17(9): 1278 - 1291.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
A.-A. Chassot, F. Ranc, E. P. Gregoire, H. L. Roepers-Gajadien, M. M. Taketo, G. Camerino, D. G. de Rooij, A. Schedl, and M.-C. Chaboissier
Activation of {beta}-catenin signaling by Rspo1 controls differentiation of the mammalian ovary
Hum. Mol. Genet., May 1, 2008; 17(9): 1264 - 1277.
[Abstract] [Full Text] [PDF]


Home page
Mol. Endocrinol.Home page
L. DiNapoli and B. Capel
SRY and the Standoff in Sex Determination
Mol. Endocrinol., January 1, 2008; 22(1): 1 - 9.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
T. Qing, H. Liu, W. Wei, X. Ye, W. Shen, D. Zhang, Z. Song, W. Yang, M. Ding, and H. Deng
Mature oocytes derived from purified mouse fetal germ cells
Hum. Reprod., January 1, 2008; 23(1): 54 - 61.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
J. Bowles and P. Koopman
Retinoic acid, meiosis and germ cell fate in mammals
Development, October 1, 2007; 134(19): 3401 - 3411.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
N. Lei, K. I Hornbaker, D. A Rice, T. Karpova, V. A Agbor, and L. L Heckert
Sex-Specific Differences in Mouse DMRT1 Expression Are Both Cell Type- and Stage-Dependent During Gonad Development
Biol Reprod, September 1, 2007; 77(3): 466 - 475.
[Abstract] [Full Text] [PDF]


Home page
ReproductionHome page
C. Itman, S. Mendis, B. Barakat, and K. L. Loveland
All in the family: TGF-{beta} family action in testis development.
Reproduction, August 1, 2006; 132(2): 233 - 246.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
L. DiNapoli, J. Batchvarov, and B. Capel
FGF9 promotes survival of germ cells in the fetal testis
Development, April 15, 2006; 133(8): 1519 - 1527.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
C. J. Guigon and S. Magre
Contribution of Germ Cells to the Differentiation and Maturation of the Ovary: Insights from Models of Germ Cell Depletion
Biol Reprod, March 1, 2006; 74(3): 450 - 458.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
J. Koubova, D. B. Menke, Q. Zhou, B. Capel, M. D. Griswold, and D. C. Page
Inaugural Articles: Retinoic acid regulates sex-specific timing of meiotic initiation in mice
PNAS, February 21, 2006; 103(8): 2474 - 2479.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
C. Ottolenghi, S. Omari, J. E. Garcia-Ortiz, M. Uda, L. Crisponi, A. Forabosco, G. Pilia, and D. Schlessinger
Foxl2 is required for commitment to ovary differentiation
Hum. Mol. Genet., July 15, 2005; 14(14): 2053 - 2062.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
C. J. Guigon, N. Coudouel, S. Mazaud-Guittot, M. G. Forest, and S. Magre
Follicular Cells Acquire Sertoli Cell Characteristics after Oocyte Loss
Endocrinology, July 1, 2005; 146(7): 2992 - 3004.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
A. Isotani, T. Nakanishi, S. Kobayashi, J. Lee, S. Chuma, N. Nakatsuji, F. Ishino, and M. Okabe
Genomic imprinting of XX spermatogonia and XX oocytes recovered from XX{leftrightarrow}XY chimeric testes
PNAS, March 15, 2005; 102(11): 4039 - 4044.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
S. Y. Park and J. L. Jameson
Minireview: Transcriptional Regulation of Gonadal Development and Differentiation
Endocrinology, March 1, 2005; 146(3): 1035 - 1042.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 2003