Literature DB >> 12412004

Different patterns of anti-Müllerian hormone expression, as related to DMRT1, SF-1, WT1, GATA-4, Wnt-4, and Lhx9 expression, in the chick differentiating gonads.

Emmanuelle Oréal1, Séverine Mazaud, Jean-Yves Picard, Solange Magre, Danièle Carré-Eusèbe.   

Abstract

In mammals, anti-Müllerian hormone (AMH) is produced by Sertoli cells from the onset of testicular differentiation and by granulosa cells after birth. In birds, AMH starts to be expressed in indifferent gonads of both sexes at a similar level and is later up-regulated in males. We previously demonstrated that, unlike in mammals, the onset of AMH expression occurs in chick embryo in the absence of SOX9. We looked for potential factors that might be involved in regulating AMH expression at different stages of chick gonad differentiation by comparing its expression pattern in embryos and young chicken with that of DMRT1, SF-1, WT1, GATA-4, Wnt-4, and Lhx9, by in situ hybridization. The results allowed us to distinguish different phases. (1) In indifferent gonads of both sexes, AMH is expressed in dispersed medullar cells. SF-1, WT1, GATA-4, Wnt-4, and DMRT1 are transcribed in the same region of the gonads, but none of these factors has an expression strictly coincident with that of AMH. Lhx9 is present only in the cortical area. (2) After this period, AMH is up-regulated in male gonads. The up-regulation is concomitant with the beginning of SOX9 expression and a sex dimorphic level of DMRT1 transcripts. It is followed by the aggregation of the AMH-positive cells (Sertoli cells) into testicular cords in which AMH is coexpressed with DMRT1, SF-1, WT1, GATA-4, and SOX9. (3) In the females, the low level of dispersed medullar AMH expression is conserved. With development of the cortex in the left ovary, cells expressing AMH accumulate in the juxtacortical part of the medulla, whereas they remain dispersed in the right ovary. At this stage, AMH expression is not strictly correlated with any of the studied factors. (4) After hatching, the organization of left ovarian cortex is characterized by the formation of follicles. Follicular cells express AMH in conjunction with SF-1, WT1, and GATA-4 and in the absence of SOX9, as in mammals. In addition, they express Lhx9 and Wnt-4, the latter being also found in the oocytes. (5) Moreover, unlike in mammals, the chicken ovary retains a dispersed AMH expression in cortical interstitial cells between the follicles, with no obvious correlation with any of the factors studied. Thus, the dispersed type of AMH expression in indifferent and female gonads appears to be bird-specific and not controlled by the same factors as testicular or follicular AMH transcription. Copyright 2002 Wiley-Liss, Inc.

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Year:  2002        PMID: 12412004     DOI: 10.1002/dvdy.10153

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  34 in total

1.  The potential role of microRNAs in regulating gonadal sex differentiation in the chicken embryo.

Authors:  Andrew D Cutting; Stephanie C Bannister; Tim J Doran; Andrew H Sinclair; Mark V L Tizard; Craig A Smith
Journal:  Chromosome Res       Date:  2012-01       Impact factor: 5.239

2.  Gene-environment interactions: the potential role of contaminants in somatic growth and the development of the reproductive system of the American alligator.

Authors:  Brandon C Moore; Alison M Roark; Satomi Kohno; Heather J Hamlin; Louis J Guillette
Journal:  Mol Cell Endocrinol       Date:  2011-10-28       Impact factor: 4.102

Review 3.  Temperature, genes, and sex: a comparative view of sex determination in Trachemys scripta and Mus musculus.

Authors:  Humphrey H-C Yao; Blanche Capel
Journal:  J Biochem       Date:  2005-07       Impact factor: 3.387

Review 4.  From gene networks underlying sex determination and gonadal differentiation to the development of neural networks regulating sociosexual behavior.

Authors:  David Crews; Wendy Lou; Alison Fleming; Sonoko Ogawa
Journal:  Brain Res       Date:  2006-08-14       Impact factor: 3.252

5.  Amh and Dmrta2 genes map to tilapia (Oreochromis spp.) linkage group 23 within quantitative trait locus regions for sex determination.

Authors:  Andrey Shirak; Eyal Seroussi; Avner Cnaani; Aimee E Howe; Raisa Domokhovsky; Noam Zilberman; Thomas D Kocher; Gideon Hulata; Micha Ron
Journal:  Genetics       Date:  2006-09-01       Impact factor: 4.562

6.  GATA4 is a key regulator of steroidogenesis and glycolysis in mouse Leydig cells.

Authors:  Anja Schrade; Antti Kyrönlahti; Oyediran Akinrinade; Marjut Pihlajoki; Merja Häkkinen; Simon Fischer; Tero-Pekka Alastalo; Vidya Velagapudi; Jorma Toppari; David B Wilson; Markku Heikinheimo
Journal:  Endocrinology       Date:  2015-02-10       Impact factor: 4.736

Review 7.  Role of the GATA family of transcription factors in endocrine development, function, and disease.

Authors:  Robert S Viger; Séverine Mazaud Guittot; Mikko Anttonen; David B Wilson; Markku Heikinheimo
Journal:  Mol Endocrinol       Date:  2008-01-03

8.  Over-expression of DMRT1 induces the male pathway in embryonic chicken gonads.

Authors:  Luke S Lambeth; Christopher S Raymond; Kelly N Roeszler; Asato Kuroiwa; Tomohiro Nakata; David Zarkower; Craig A Smith
Journal:  Dev Biol       Date:  2014-02-24       Impact factor: 3.582

9.  GATA4 Regulates Blood-Testis Barrier Function and Lactate Metabolism in Mouse Sertoli Cells.

Authors:  Anja Schrade; Antti Kyrönlahti; Oyediran Akinrinade; Marjut Pihlajoki; Simon Fischer; Verena Martinez Rodriguez; Kerstin Otte; Vidya Velagapudi; Jorma Toppari; David B Wilson; Markku Heikinheimo
Journal:  Endocrinology       Date:  2016-03-14       Impact factor: 4.736

10.  OVEX1, a novel chicken endogenous retrovirus with sex-specific and left-right asymmetrical expression in gonads.

Authors:  Danièle Carré-Eusèbe; Noëlline Coudouel; Solange Magre
Journal:  Retrovirology       Date:  2009-06-17       Impact factor: 4.602

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