Literature DB >> 18182450

Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and müllerian duct abnormalities: a French collaborative study.

Pascal Philibert1, Anna Biason-Lauber, Roman Rouzier, Catherine Pienkowski, Françoise Paris, Daniel Konrad, Eugene Schoenle, Charles Sultan.   

Abstract

CONTEXT: Müllerian duct development depends on gene and hormone interactions. Female Wnt4-knockout mice lack müllerian ducts and are virilized due to the inappropriate expression of the enzymes required for androgen production (normally repressed in female ovary). The WNT4 mutation was recently reported to be associated with failure of müllerian duct formation and virilization in two 46, XX women.
OBJECTIVES: This collaborative work was designed to determine whether the WNT4 mutation could be identified in a group of adolescent girls with Mayer-Rokitansky-Küster-Hauser syndrome.
RESULTS: We analyzed 28 DNA samples from adolescent girls with primary amenorrhea and failure of müllerian duct formation by direct sequencing and identified a new L12P mutation within exon 1 of the WNT4 gene. The substitution of leucine by proline is crucial for the conformation of the expressed protein. This amino acid substitution is unlikely to be a polymorphism because it was not found in 100 DNAs from control subjects. Functional analysis revealed that the mutation induces significantly increased expression of the enzymes involved in androgen biosynthesis (3beta-hydroxysteroid dehydrogenase and 17alpha-hydroxylase). It is interesting to note that the adolescent carrying the mutation was referred to our clinic for primary amenorrhea and hyperandrogenism (severe acne and plasma testosterone: 1.8 vs. 1.2 nmol/liter in controls). She also presented with uterine hypoplasia and follicle depletion.
CONCLUSIONS: We suggest that in adolescent girls with primary amenorrhea, müllerian duct abnormalities, and hyperandrogenism, a WNT4 mutation should be sought. Moreover, our data confirm that WNT4 is involved in the regulation of müllerian duct development and ovarian androgen biosynthesis. WNT4 may also contribute to human follicle development and/or maintenance.

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Year:  2008        PMID: 18182450     DOI: 10.1210/jc.2007-2023

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  45 in total

1.  Wnt4, the first member of the Wnt family identified in Schistosoma japonicum, regulates worm development by the canonical pathway.

Authors:  Hong-Fei Li; Xiao-Bo Wang; Ya-Ping Jin; Yan-Xun Xia; Xin-Gang Feng; Jian-Mei Yang; Xin-Yong Qi; Chun-Xiu Yuan; Jiao-Jiao Lin
Journal:  Parasitol Res       Date:  2010-06-24       Impact factor: 2.289

2.  Wnt family member 4 (WNT4) and WNT3A activate cell-autonomous Wnt signaling independent of porcupine O-acyltransferase or Wnt secretion.

Authors:  Deviyani M Rao; Madeleine T Shackleford; Evelyn K Bordeaux; Joseph L Sottnik; Rebecca L Ferguson; Tomomi M Yamamoto; Elizabeth A Wellberg; Benjamin G Bitler; Matthew J Sikora
Journal:  J Biol Chem       Date:  2019-11-18       Impact factor: 5.157

3.  Association of WNT4 polymorphisms with endometriosis in infertile patients.

Authors:  Fernanda Mafra; Michele Catto; Bianca Bianco; Caio Parente Barbosa; Denise Christofolini
Journal:  J Assist Reprod Genet       Date:  2015-07-03       Impact factor: 3.412

4.  Genetic Screening of Iranian Patients with 46,XY Disorders of Sex Development.

Authors:  Azadeh Shojaei; Reza Ebrahimzadeh-Vesal; Ali Ahani; Maryam Razzaghy-Azar; Golnaz Khakpour; Farideh Ghazi; Javad Tavakkoly-Bazzaz
Journal:  Rep Biochem Mol Biol       Date:  2017-10

5.  Genetic analysis of Mayer-Rokitansky-Kuster-Hauser syndrome in a large cohort of families.

Authors:  Lacey S Williams; Durkadin Demir Eksi; Yiping Shen; Amy C Lossie; Lynn P Chorich; Megan E Sullivan; John A Phillips; Munire Erman; Hyung-Goo Kim; Ozgul M Alper; Lawrence C Layman
Journal:  Fertil Steril       Date:  2017-06-07       Impact factor: 7.329

Review 6.  Building pathways for ovary organogenesis in the mouse embryo.

Authors:  Chia-Feng Liu; Chang Liu; Humphrey H-C Yao
Journal:  Curr Top Dev Biol       Date:  2010       Impact factor: 4.897

Review 7.  The genetic basis of female reproductive disorders: etiology and clinical testing.

Authors:  Lawrence C Layman
Journal:  Mol Cell Endocrinol       Date:  2013-03-14       Impact factor: 4.102

8.  Molecular analysis of the beta-catenin gene in patients with the Mayer-Rokitansky-Küster-Hauser syndrome.

Authors:  Juliana B Drummond; Camila F Rezende; Fabio C Peixoto; Joana S Carvalho; Fernando M Reis; Luiz De Marco
Journal:  J Assist Reprod Genet       Date:  2008-11-01       Impact factor: 3.412

9.  Congenital Malformations of the Reproductive Tract in a Patient with Poland Syndrome: Is There a Connection?

Authors:  Tian Meng; Ming Bai; Ru Zhao
Journal:  Breast Care (Basel)       Date:  2017-10-27       Impact factor: 2.860

Review 10.  WNT4 Balances Development vs Disease in Gynecologic Tissues and Women's Health.

Authors:  Lauren M Pitzer; Marisa R Moroney; Natalie J Nokoff; Matthew J Sikora
Journal:  Endocrinology       Date:  2021-07-01       Impact factor: 4.736

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