Suppr超能文献

小鼠卵睾体发育过程中睾丸和卵巢决定途径的拮抗作用。

Antagonism of the testis- and ovary-determining pathways during ovotestis development in mice.

作者信息

Wilhelm Dagmar, Washburn Linda L, Truong Vy, Fellous Marc, Eicher Eva M, Koopman Peter

机构信息

Division of Molecular Genetics and Development, Institute for Molecular Biosciences, The University of Queensland, Qld, Australia.

出版信息

Mech Dev. 2009 May-Jun;126(5-6):324-36. doi: 10.1016/j.mod.2009.02.006. Epub 2009 Mar 6.

Abstract

Ovotestis development in B6-XY(POS) mice provides a rare opportunity to study the interaction of the testis- and ovary-determining pathways in the same tissue. We studied expression of several markers of mouse fetal testis (SRY, SOX9) or ovary (FOXL2, Rspo1) development in B6-XY(POS) ovotestes by immunofluorescence, using normal testes and ovaries as controls. In ovotestes, SOX9 was expressed only in the central region where SRY is expressed earliest, resulting in testis cord formation. Surprisingly, FOXL2-expressing cells also were found in this region, but individual cells expressed either FOXL2 or SOX9, not both. At the poles, even though SOX9 was not up-regulated, SRY expression was down-regulated normally as in XY testes, and FOXL2 was expressed from an early stage, demonstrating ovarian differentiation in these areas. Our data (1) show that SRY must act within a specific developmental window to activate Sox9; (2) challenge the established view that SOX9 is responsible for down-regulating Sry expression; (3) disprove the concept that testicular and ovarian cells occupy discrete domains in ovotestes; and (4) suggest that FOXL2 is actively suppressed in Sertoli cell precursors by the action of SOX9. Together these findings provide important new insights into the molecular regulation of testis and ovary development.

摘要

B6-XY(POS)小鼠的卵睾体发育为研究睾丸和卵巢决定途径在同一组织中的相互作用提供了一个难得的机会。我们通过免疫荧光研究了B6-XY(POS)卵睾体中小鼠胎儿睾丸(SRY、SOX9)或卵巢(FOXL2、Rspo1)发育的几种标志物的表达情况,以正常睾丸和卵巢作为对照。在卵睾体中,SOX9仅在SRY最早表达的中央区域表达,从而导致睾丸索形成。令人惊讶的是,在该区域也发现了表达FOXL2的细胞,但单个细胞要么表达FOXL2,要么表达SOX9,不会同时表达两者。在两极,尽管SOX9没有上调,但SRY的表达如在XY睾丸中一样正常下调,并且FOXL2从早期就开始表达,表明这些区域发生了卵巢分化。我们的数据(1)表明SRY必须在特定的发育窗口期内发挥作用以激活Sox9;(2)对SOX9负责下调Sry表达这一既定观点提出了挑战;(3)反驳了睾丸细胞和卵巢细胞在卵睾体中占据离散区域的概念;(4)表明在支持细胞前体中,FOXL2受到SOX9作用的积极抑制。这些发现共同为睾丸和卵巢发育的分子调控提供了重要的新见解。

相似文献

1
Antagonism of the testis- and ovary-determining pathways during ovotestis development in mice.
Mech Dev. 2009 May-Jun;126(5-6):324-36. doi: 10.1016/j.mod.2009.02.006. Epub 2009 Mar 6.
3
SRY upregulation of SOX9 is inefficient and delayed, allowing ovarian differentiation, in the B6.Y(TIR) gonad.
Differentiation. 2011 Jul;82(1):18-27. doi: 10.1016/j.diff.2011.04.007. Epub 2011 May 17.
4
Testis Determination Requires a Specific FGFR2 Isoform to Repress FOXL2.
Endocrinology. 2017 Nov 1;158(11):3832-3843. doi: 10.1210/en.2017-00674.
6
Antagonistic regulation of Cyp26b1 by transcription factors SOX9/SF1 and FOXL2 during gonadal development in mice.
FASEB J. 2011 Oct;25(10):3561-9. doi: 10.1096/fj.11-184333. Epub 2011 Jul 14.
8
DMRT1 prevents female reprogramming in the postnatal mammalian testis.
Nature. 2011 Jul 20;476(7358):101-4. doi: 10.1038/nature10239.
9
Gadd45g is required for timely Sry expression independently of RSPO1 activity.
Reproduction. 2022 Apr 22;163(6):333-340. doi: 10.1530/REP-21-0443.
10
Correct dosage of Fog2 and Gata4 transcription factors is critical for fetal testis development in mice.
Proc Natl Acad Sci U S A. 2007 Sep 18;104(38):14994-9. doi: 10.1073/pnas.0701677104. Epub 2007 Sep 11.

引用本文的文献

2
KDM6B is a conserved activator at the top of the male sex determination pathway.
Development. 2025 Jun 15;152(12). doi: 10.1242/dev.204724. Epub 2025 Jun 13.
3
Gonadal sex reversal at single-cell resolution in Znrf3-deficient mice.
Development. 2024 Dec 1;151(23). doi: 10.1242/dev.202707. Epub 2024 Dec 4.
4
Specificity of Key Sex Determination Genes in a Mammal with Ovotestes: The European Mole .
Animals (Basel). 2024 Jul 26;14(15):2180. doi: 10.3390/ani14152180.
5
Genomic technologies and the diagnosis of 46, XY differences of sex development.
Andrology. 2025 Jul;13(5):1025-1043. doi: 10.1111/andr.13708. Epub 2024 Jul 31.
6
Testicular differentiation in 46,XX DSD: an overview of genetic causes.
Front Endocrinol (Lausanne). 2024 Apr 24;15:1385901. doi: 10.3389/fendo.2024.1385901. eCollection 2024.
7
Reconstituted ovaries self-assemble without an ovarian surface epithelium.
Stem Cell Reports. 2023 Nov 14;18(11):2190-2202. doi: 10.1016/j.stemcr.2023.10.001. Epub 2023 Oct 26.
8
A Rare Differences of Sex Development: Male Sex Reversal Syndrome (NonSyndromic 46, XX with Negative Sex-Determining Region of Y Chromosome Gene).
J Indian Assoc Pediatr Surg. 2023 Mar-Apr;28(2):154-159. doi: 10.4103/jiaps.jiaps_109_22. Epub 2022 Nov 30.
9
Biased precursor ingression underlies the center-to-pole pattern of male sex determination in mouse.
Development. 2023 Mar 1;150(5). doi: 10.1242/dev.201060. Epub 2023 Mar 13.
10
Avian Sex Determination: A Chicken and Egg Conundrum.
Sex Dev. 2023;17(2-3):120-133. doi: 10.1159/000529754. Epub 2023 Feb 16.

本文引用的文献

1
A critical time window of Sry action in gonadal sex determination in mice.
Development. 2009 Jan;136(1):129-38. doi: 10.1242/dev.029587. Epub 2008 Nov 26.
2
Sex determination involves synergistic action of SRY and SF1 on a specific Sox9 enhancer.
Nature. 2008 Jun 12;453(7197):930-4. doi: 10.1038/nature06944. Epub 2008 May 4.
4
Activation of beta-catenin signaling by Rspo1 controls differentiation of the mammalian ovary.
Hum Mol Genet. 2008 May 1;17(9):1264-77. doi: 10.1093/hmg/ddn016. Epub 2008 Feb 4.
5
R-spondin1 plays an essential role in ovarian development through positively regulating Wnt-4 signaling.
Hum Mol Genet. 2008 May 1;17(9):1278-91. doi: 10.1093/hmg/ddn036. Epub 2008 Feb 4.
6
Loss of Wnt4 and Foxl2 leads to female-to-male sex reversal extending to germ cells.
Hum Mol Genet. 2007 Dec 1;16(23):2795-804. doi: 10.1093/hmg/ddm235. Epub 2007 Aug 29.
7
SOX9 regulates prostaglandin D synthase gene transcription in vivo to ensure testis development.
J Biol Chem. 2007 Apr 6;282(14):10553-60. doi: 10.1074/jbc.M609578200. Epub 2007 Feb 2.
8
R-spondin1 is essential in sex determination, skin differentiation and malignancy.
Nat Genet. 2006 Nov;38(11):1304-9. doi: 10.1038/ng1907. Epub 2006 Oct 15.
9
The poly(ADP-ribose) polymerase 1 interacts with Sry and modulates its biological functions.
Mol Cell Endocrinol. 2006 Sep 26;257-258:35-46. doi: 10.1016/j.mce.2006.06.008. Epub 2006 Aug 9.
10
The makings of maleness: towards an integrated view of male sexual development.
Nat Rev Genet. 2006 Aug;7(8):620-31. doi: 10.1038/nrg1903. Epub 2006 Jul 11.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验